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Latest revision as of 20:47, 12 September 2019

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Mandana Chitsazan, M.D. [2]

Synonyms and keywords:Mesothelioma of the AV node, AV node tumor

Overview

Cystic tumor of the atrioventricular (AV) node is a rare benign congenital tumor. The origin of the cystic tumor of the AV node is still controversial. Although it is called mesothelioma of the AV node, it appears to have endodermal origin. The size of the tumor ranges from 0.5 mm to 30 mm and size of the tumor is not correlated with the occurrence of fatal arrhythmias. On gross pathology, small multiocular cysts are characteristic findings of the cystic tumor of the AV node. On microscopic examination, solid cell nests and cystic structures lined by flattended cuboidal and squamous epithelium mixed with rare neuroendocrine cells (C cells) are characteristic findings of the cystic tumor of the AV node. The immunohistochemical staining of the cystic tumor of the AV node is in favor of the epithelial differentiation of the tumor. Cystic tumor of the AV node is most commonly diagnosed postmortem in individuals died due to sudden cardiac death. Fatal arrhythmias including ventricular tachycardia or ventricular fibrillation may occur despite pacemaker placement. Only a few cases of cystic tumor of the AV node has been diagnosed antemortem. Imaging modalities including echocardiography and MRI are helpful in making the diagnosis. Histopathological examination of the resected tumor provides the definitive diagnosis. Because of the critical location of the tumor and its unfavorable prognosis, surgical excision is the mainstay of treatment for cystic tumor of the AV node. Anti-arrhythmic drugs and lifelong pacemaker placement may be necessary after excision to manage any post-surgical AV block.

Historical Perspective

Cystic tumor of the atrioventricular (AV) node was first reported by Armstrong and Mönckeberg in 1911. ^[1]

Classification

There is no established system for the staging of the cystic tumor of the AV node.

Pathophysiology

The cystic tumor of the AV node is a benign congenital tumor. Although it is also called mesothelioma of the AV node, it appears to be a misnomer. The origin of the cystic tumor of the AV node is still controversial. It is believed that it has endodermal origin, derived from congenital rests during embryogenesis. ^[2] ^[3] One study suggested that cystic tumor of the AV node and solid cell nests of the thyroid have similar structures and may share the same developmental process; therefore it is assumed that cystic tumor of the AV node is an ultimobranchial heterotopia. ^[4]

On gross pathology, small multiocular cysts are characteristic findings of the cystic tumor of the AV node. The tumor may be invisible from the endocardial surface of the heart. Therefore, sectioning through the infero-medial tricuspid annulus might be required. ^[5] ^[6] The size of the tumor ranges from 0.5 mm to 30 mm and the size of the tumor is not correlated with the occurrence of fatal arrhythmias. ^[7]

On microscopic histopathological analysis, solid cell nests and cystic structures lined by flattened cuboidal or squamous epithelium mixed with rare neuroendocrine cells (C cells) are characteristic findings of the cystic tumor of the AV node. ^[5] ^[6] ^[8]

On immunohistochemical staining, the main tumor cells stain positive for: ^[9]

Cytokeratin CAM5.2
Cytokeratin AE1/AE3
Cytokeratin 34βE12
Cytokeratin 5/6 (CK5/6)
Cytokeratin 7 (CK7)
Epithelial membrane antigen (EMA)
Carcinoembryonic antigen (CEA)
Carbohydrate antigen (CA)19.9
p63
bcl2
Galectin-3

The neuroendocrine cells of the lesion stain positive for: ^[10] ^[8] ^[9]

CAM5.2
Pan-keratin (AE1/AE3)
CEA
Calcitonin
Chromogranin
Synaptophysin
hyroid Transcription Factor 1 (TTF1)

The tumor stains negative for: ^[10] ^[8] ^[9]

However, true mesothelium stains positive for thrombomodulin, Wilm’s tumor 1, calretinin and negative for PAS. ^[11]

The immunohistochemistry staining of the cystic tumor of the AV node is in favor of the epithelial differentiation of the tumor and supports the labeling of this tumor as an endodermal heterotopia. ^[10]

Causes

The cause of the cystic tumor of the AV node has not been identified. Other mid-line developmental defects are seen in 10% of the patients. ^[6]It suggests that a genetic defect might involve migration of embryological tissues and cardiac neural crest cell development ^[4] ^[2] with possible familial predisposition. ^[12] Considering the absence of mitoses in the tumor, it is suggested to be resulted from a dilatation of cystic spaces rather than true neoplasm. ^[13] ^[14]

Differentiating Cystic Tumor of the AV node from Other Diseases

Cystic tumor of the AV node must be differentiated from other cardiac tumors.

Epidemiology and Demographics

Primary cardiac tumors are rare with an incidence of 0.0017% to 0.03% of all autopsies. ^[6] ^[5] Cystic tumor of the AV node accounts for 2.7% of cardiac tumors and it is the most common primary cardiac tumor that causes sudden death. ^[6] ^[15]

There is no racial or ethnic predilection to the cystic tumor of the AV node.

Women are more commonly affected by the cystic tumor of the AV node than men. The female to male ratio is approximately 3 to 1. ^[5]

The cystic tumor of the AV node is usually diagnosed in the fourth decade of life. ^[6]

Risk Factors

There are no established risk factors for the cystic tumor of the AV node.

Screening

There is insufficient evidence to recommend routine screening for the cystic tumor of the AV node.

Natural History, Complications, and Prognosis

Cystic tumor of the AV node is most commonly diagnosed postmortem in individuals died due to sudden cardiac death. Fatal arrhythmias including ventricular tachycardia or ventricular fibrillation may occur despite pacemaker placement. ^[16] ^[17]

Diagnosis

Diagnostic Study of Choice

There are no established criteria for the diagnosis of cystic tumor of the AV node. Only a few cases of cystic tumor of the AV node has been diagnosed antemortem. Imaging modalities including echocardiography and MRI are helpful in making the diagnosis. ^[18] Histopathological examination of the resected tumor provides the definitive diagnosis. ^[18]

History and Symptoms

The presentation of the cystic tumor of the AV node can range from being asymptomatic to sudden cardiac death. ^[17]^[18] Typical symptoms are: ^[8] ^[19]^[20] ^[21]

Patients may also present with partial or complete heart block. ^[20] ^[22] ^[16]

Physical Examination

Physical examination of patients with cystic tumor of the AV node is usually unremarkable.

Laboratory Findings

There are no diagnostic laboratory findings associated with cystic tumor of the AV node.

Electrocardiogram

An ECG may be helpful in the diagnosis of cystic tumor of the AV node. ECG might show partial or complete heart block. ^[20]^[19]^[23]

X-ray

There are no x-ray findings associated with cystic tumor of the AV node.

Echocardiography or Ultrasound

Echocardiography may be helpful in the diagnosis of cystic tumor of the AV node, showing a mass at the site of the tumor. ^[19] ^[20] ^[23]

CT scan

Only a few cases of cystic tumor of the AV node have been reported antemortem. Therefore, the data regarding the imaging findings are limited. Reports have shown either a high-attenuation ^[24] or low-attenuation lesions on CT images. ^[25]

MRI

Cardiac MRI may be helpful in the diagnosis of the cystic tumor of the AV node. High-signal intensity lesion on T1-weighted ^[8] ^[24] ^[18]and T2-weighted MRI ^[24] or low signal intensity on T2-weighted MRI ^[18] have been reported.

Other Imaging Findings

There are no other imaging findings associated with cystic tumor of the AV node.

Other Diagnostic Studies

There are no other diagnostic studies associated with cystic tumor of the AV node.

Treatment

Medical Therapy

There is no medical treatment for the cystic tumor of the AV node.

Surgery

Because of the critical location of the tumor and its unfavorable prognosis, surgical excision is the mainstay of treatment for cystic tumor of the AV node. Anti-arrhythmic drugs and lifelong pacemaker placement may be necessary after excision to manage any post-surgical AV block. ^[5] ^[6]

Primary Prevention

There are no established measures for the primary prevention of the cystic tumor of the AV node.

Secondary Prevention

There are no established measures for the secondary prevention of the cystic tumor of the AV node.

References

↑ Armstrong H, Mönckeberg JG (1911). "Herzblock, bedingt durch primären Herztumor, bei einem 5 jährigen Kinde". Dtsch Arch Klin Med. 102: 144–146.
↑ ^2.0 ^2.1 Burke AP, Anderson PG, Virmani R, James TN, Herrera GA, Ceballos R (1990). "Tumor of the atrioventricular nodal region. A clinical and immunohistochemical study". Arch Pathol Lab Med. 114 (10): 1057–62. PMID 2222148.
↑ Cameselle-Teijeiro J, Santías RR, Nallib IA, Forteza J, Barreiro NA (2010). "Cystic tumor of the atrioventricular node: a rare cardiac pseudoneoplastic lesion". Arch Pathol Lab Med. 134 (11): 1584–6. doi:10.1043/2010-0268-LER.1. PMID 21043810.
↑ ^4.0 ^4.1 Cameselle-Teijeiro J, Abdulkader I, Soares P, Alfonsín-Barreiro N, Moldes-Boullosa J, Sobrinho-Simões M (2005). "Cystic tumor of the atrioventricular node of the heart appears to be the heart equivalent of the solid cell nests (ultimobranchial rests) of the thyroid". Am J Clin Pathol. 123 (3): 369–75. doi:10.1309/GWT2-PY0T-77PB-BA1A. PMID 15716232.
↑ ^5.0 ^5.1 ^5.2 ^5.3 ^5.4 Miller DV (2012). "Cardiac Tumors". Surg Pathol Clin. 5 (2): 453–83. doi:10.1016/j.path.2012.04.007. PMID 26838113.
↑ ^6.0 ^6.1 ^6.2 ^6.3 ^6.4 ^6.5 ^6.6 Burke A, Tavora F (2016). "The 2015 WHO Classification of Tumors of the Heart and Pericardium". J Thorac Oncol. 11 (4): 441–52. doi:10.1016/j.jtho.2015.11.009. PMID 26725181.
↑ Guo J, Zuo S, Lin C, Ji Y (May 2009). "Surgical treatment of a giant cystic tumor of the atrioventricular nodal region". Interact Cardiovasc Thorac Surg. 8 (5): 592–3. doi:10.1510/icvts.2008.191866. PMID 19237400.
↑ ^8.0 ^8.1 ^8.2 ^8.3 ^8.4 Paniagua JR, Sadaba JR, Davidson LA, Munsch CM (2000). "Cystic tumour of the atrioventricular nodal region: report of a case successfully treated with surgery". Heart. 83 (4): E6. doi:10.1136/heart.83.4.e6. PMC 1729374. PMID 10722558.
↑ ^9.0 ^9.1 ^9.2 Arai T, Kurashima C, Wada S, Chida K, Ohkawa S (1998). "Histological evidence for cell proliferation activity in cystic tumor (endodermal heterotopia) of the atrioventricular node". Pathol Int. 48 (11): 917–23. PMID 9832064.
↑ ^10.0 ^10.1 ^10.2 Evans CA, Suvarna SK (2005). "Cystic atrioventricular node tumour: not a mesothelioma". J Clin Pathol. 58 (11): 1232. PMC 1770778. PMID 16254122.
↑ Fletcher, Christopher (2013). Diagnostic histopathology of tumors. Philadelphia, PA: Saunders/Elsevier. ISBN 9781437715347.
↑ Travers H (1985). "Congenital polycystic tumor of the atrioventricular node". Arch Pathol Lab Med. 109 (8): 704–6. PMID 3839372.
↑ Thorgeirsson G, Liebman J (1983). "Mesothelioma of the AV node". Pediatr Cardiol. 4 (3): 219–23. doi:10.1007/BF02242259. PMID 6647106.
↑ Ford SE (1999). "Congenital cystic tumors of the atrio-ventricular node: successful demonstration by an abbreviated dissection of the conduction system". Cardiovasc Pathol. 8 (4): 233–7. PMID 10724528.
↑ Wolf PL, Bing R (1965). "The smallest tumor which causes sudden death". JAMA. 194 (6): 674–5. PMID 5897246.
↑ ^16.0 ^16.1 Maujean G, Tabib A, Malicier D, Fanton L (2010). "Sudden death due to a cystic atrio-ventricular node tumour". J Forensic Leg Med. 17 (8): 437–8. doi:10.1016/j.jflm.2010.08.009. PMID 21056880.
↑ ^17.0 ^17.1 Patel J, Sheppard MN (2011). "Cystic tumour of the atrioventricular node: three cases of sudden death". Int J Legal Med. 125 (1): 139–42. doi:10.1007/s00414-009-0399-7. PMID 20020153.
↑ ^18.0 ^18.1 ^18.2 ^18.3 ^18.4 Suzuki K, Matsushita S, Suzuki H, Kuroda K, Inaba H, Arakawa A; et al. (2014). "Cystic tumor of the atrioventricular node: computed tomography and magnetic resonance imaging findings". J Thorac Imaging. 29 (6): W97–9. doi:10.1097/RTI.0000000000000111. PMID 25303965.
↑ ^19.0 ^19.1 ^19.2 Abuzeid W, Myers R (April 2017). "Cystic tumour of the atrioventricular node: treatment dilemma". BMJ Case Rep. 2017. doi:10.1136/bcr-2017-219314. PMC 5534749. PMID 28438795. Vancouver style error: initials (help)
↑ ^20.0 ^20.1 ^20.2 ^20.3 Law KB, Feng T, Nair V, Cusimano RJ, Butany J (2012). "Cystic tumor of the atrioventricular node: rare antemortem diagnosis". Cardiovasc Pathol. 21 (2): 120–7. doi:10.1016/j.carpath.2011.05.004. PMID 21820324.
↑ Lewman LV, Demany MA, Zimmerman HA (1972). "Congenital tumor of atrioventricular node with complete heart block and sudden death. Mesothelioma or lymphangio-endothelioma of atrioventricular node". Am J Cardiol. 29 (4): 554–7. doi:10.1016/0002-9149(72)90448-1. PMID 5016834.
↑ Hopkinson JM, Newcombe CP (1971). "Heart block due to epithelial heterotopia". J Pathol. 104 (3): 218–20. doi:10.1002/path.1711040312. PMID 5124984.
↑ ^23.0 ^23.1 Careddu L, Pantaleo A, Savini C, Di Eusanio M, Leone O, Di Bartolomeo R (2013). "Cystic atrioventricular node tumor excision by minimally invasive surgery". Ann Thorac Surg. 96 (5): 1873–5. doi:10.1016/j.athoracsur.2013.03.036. PMID 24182482.
↑ ^24.0 ^24.1 ^24.2 Saito S, Kobayashi J, Tagusari O, Bando K, Niwaya K, Nakajima H; et al. (2005). "Successful excision of a cystic tumor of the atrioventricular nodal region". Circ J. 69 (10): 1293–4. PMID 16195634.
↑ Kaminishi Y, Watanabe Y, Nakata H; et al. (2002). "Cystic tumor of the atrioventricular nodal region". . Jpn J Thorac Cardiovasc Surg. 50: 37–39.

Template:WikiDoc Sources

[Armstrong-1] Armstrong H, Mönckeberg JG (1911). "Herzblock, bedingt durch primären Herztumor, bei einem 5 jährigen Kinde". Dtsch Arch Klin Med. 102: 144–146.

[pmid2222148-2] 2.0 ^2.1 Burke AP, Anderson PG, Virmani R, James TN, Herrera GA, Ceballos R (1990). "Tumor of the atrioventricular nodal region. A clinical and immunohistochemical study". Arch Pathol Lab Med. 114 (10): 1057–62. PMID 2222148.

[pmid21043810-3] Cameselle-Teijeiro J, Santías RR, Nallib IA, Forteza J, Barreiro NA (2010). "Cystic tumor of the atrioventricular node: a rare cardiac pseudoneoplastic lesion". Arch Pathol Lab Med. 134 (11): 1584–6. doi:10.1043/2010-0268-LER.1. PMID 21043810.

[pmid15716232-4] 4.0 ^4.1 Cameselle-Teijeiro J, Abdulkader I, Soares P, Alfonsín-Barreiro N, Moldes-Boullosa J, Sobrinho-Simões M (2005). "Cystic tumor of the atrioventricular node of the heart appears to be the heart equivalent of the solid cell nests (ultimobranchial rests) of the thyroid". Am J Clin Pathol. 123 (3): 369–75. doi:10.1309/GWT2-PY0T-77PB-BA1A. PMID 15716232.

[pmid26838113-5] 5.0 ^5.1 ^5.2 ^5.3 ^5.4 Miller DV (2012). "Cardiac Tumors". Surg Pathol Clin. 5 (2): 453–83. doi:10.1016/j.path.2012.04.007. PMID 26838113.

[pmid26725181-6] 6.0 ^6.1 ^6.2 ^6.3 ^6.4 ^6.5 ^6.6 Burke A, Tavora F (2016). "The 2015 WHO Classification of Tumors of the Heart and Pericardium". J Thorac Oncol. 11 (4): 441–52. doi:10.1016/j.jtho.2015.11.009. PMID 26725181.

[pmid19237400-7] Guo J, Zuo S, Lin C, Ji Y (May 2009). "Surgical treatment of a giant cystic tumor of the atrioventricular nodal region". Interact Cardiovasc Thorac Surg. 8 (5): 592–3. doi:10.1510/icvts.2008.191866. PMID 19237400.

[pmid10722558-8] 8.0 ^8.1 ^8.2 ^8.3 ^8.4 Paniagua JR, Sadaba JR, Davidson LA, Munsch CM (2000). "Cystic tumour of the atrioventricular nodal region: report of a case successfully treated with surgery". Heart. 83 (4): E6. doi:10.1136/heart.83.4.e6. PMC 1729374. PMID 10722558.

[pmid9832064-9] 9.0 ^9.1 ^9.2 Arai T, Kurashima C, Wada S, Chida K, Ohkawa S (1998). "Histological evidence for cell proliferation activity in cystic tumor (endodermal heterotopia) of the atrioventricular node". Pathol Int. 48 (11): 917–23. PMID 9832064.

[pmid16254122-10] 10.0 ^10.1 ^10.2 Evans CA, Suvarna SK (2005). "Cystic atrioventricular node tumour: not a mesothelioma". J Clin Pathol. 58 (11): 1232. PMC 1770778. PMID 16254122.

[11] Fletcher, Christopher (2013). Diagnostic histopathology of tumors. Philadelphia, PA: Saunders/Elsevier. ISBN 9781437715347.

[pmid3839372-12] Travers H (1985). "Congenital polycystic tumor of the atrioventricular node". Arch Pathol Lab Med. 109 (8): 704–6. PMID 3839372.

[pmid6647106-13] Thorgeirsson G, Liebman J (1983). "Mesothelioma of the AV node". Pediatr Cardiol. 4 (3): 219–23. doi:10.1007/BF02242259. PMID 6647106.

[pmid10724528-14] Ford SE (1999). "Congenital cystic tumors of the atrio-ventricular node: successful demonstration by an abbreviated dissection of the conduction system". Cardiovasc Pathol. 8 (4): 233–7. PMID 10724528.

[pmid5897246-15] Wolf PL, Bing R (1965). "The smallest tumor which causes sudden death". JAMA. 194 (6): 674–5. PMID 5897246.

[pmid21056880-16] 16.0 ^16.1 Maujean G, Tabib A, Malicier D, Fanton L (2010). "Sudden death due to a cystic atrio-ventricular node tumour". J Forensic Leg Med. 17 (8): 437–8. doi:10.1016/j.jflm.2010.08.009. PMID 21056880.

[pmid20020153-17] 17.0 ^17.1 Patel J, Sheppard MN (2011). "Cystic tumour of the atrioventricular node: three cases of sudden death". Int J Legal Med. 125 (1): 139–42. doi:10.1007/s00414-009-0399-7. PMID 20020153.

[pmid25303965-18] 18.0 ^18.1 ^18.2 ^18.3 ^18.4 Suzuki K, Matsushita S, Suzuki H, Kuroda K, Inaba H, Arakawa A; et al. (2014). "Cystic tumor of the atrioventricular node: computed tomography and magnetic resonance imaging findings". J Thorac Imaging. 29 (6): W97–9. doi:10.1097/RTI.0000000000000111. PMID 25303965.

[pmid28438795-19] 19.0 ^19.1 ^19.2 Abuzeid W, Myers R (April 2017). "Cystic tumour of the atrioventricular node: treatment dilemma". BMJ Case Rep. 2017. doi:10.1136/bcr-2017-219314. PMC 5534749. PMID 28438795. Vancouver style error: initials (help)

[pmid21820324-20] 20.0 ^20.1 ^20.2 ^20.3 Law KB, Feng T, Nair V, Cusimano RJ, Butany J (2012). "Cystic tumor of the atrioventricular node: rare antemortem diagnosis". Cardiovasc Pathol. 21 (2): 120–7. doi:10.1016/j.carpath.2011.05.004. PMID 21820324.

[pmid5016834-21] Lewman LV, Demany MA, Zimmerman HA (1972). "Congenital tumor of atrioventricular node with complete heart block and sudden death. Mesothelioma or lymphangio-endothelioma of atrioventricular node". Am J Cardiol. 29 (4): 554–7. doi:10.1016/0002-9149(72)90448-1. PMID 5016834.

[pmid5124984-22] Hopkinson JM, Newcombe CP (1971). "Heart block due to epithelial heterotopia". J Pathol. 104 (3): 218–20. doi:10.1002/path.1711040312. PMID 5124984.

[pmid24182482-23] 23.0 ^23.1 Careddu L, Pantaleo A, Savini C, Di Eusanio M, Leone O, Di Bartolomeo R (2013). "Cystic atrioventricular node tumor excision by minimally invasive surgery". Ann Thorac Surg. 96 (5): 1873–5. doi:10.1016/j.athoracsur.2013.03.036. PMID 24182482.

[pmid16195634-24] 24.0 ^24.1 ^24.2 Saito S, Kobayashi J, Tagusari O, Bando K, Niwaya K, Nakajima H; et al. (2005). "Successful excision of a cystic tumor of the atrioventricular nodal region". Circ J. 69 (10): 1293–4. PMID 16195634.

[Kaminishi-25] Kaminishi Y, Watanabe Y, Nakata H; et al. (2002). "Cystic tumor of the atrioventricular nodal region". . Jpn J Thorac Cardiovasc Surg. 50: 37–39.

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@@ Line 4: / Line 4: @@
 {{CMG}}; {{AE}} {{MC}}
-{{SK}} Mesothelioma of the atrioventricular node
+{{SK}}Mesothelioma of the AV node, AV node tumor
 ==Overview==
+Cystic tumor of the atrioventricular (AV) node is a [[rare]] [[benign]] [[congenital]] [[tumor]]. The [[origin]] of the cystic tumor of the AV node is still controversial. Although it is called [[mesothelioma]] of the AV node, it appears to have [[Endoderm|endodermal]] origin. The size of the [[tumor]] ranges from 0.5 mm to 30 mm and size of the tumor is not correlated with the occurrence of [[fatal]] [[arrhythmias]]. On [[gross pathology]], small multiocular [[Cyst|cysts]] are characteristic findings of the cystic tumor of the AV node. On [[microscopic examination]], [[solid]] [[cell]] nests and [[cystic]] structures lined by flattended [[Cuboidal epithelium|cuboidal]] and [[squamous epithelium]] mixed with rare [[neuroendocrine cells]] ([[C cells]]) are characteristic findings of the cystic tumor of the AV node. The [[immunohistochemical staining]] of the cystic tumor of the AV node is in favor of the [[epithelial]] [[differentiation]] of the tumor. Cystic tumor of the AV node is most commonly [[Diagnose|diagnosed]] [[postmortem]] in individuals died due to [[sudden cardiac death]]. [[Fatal arrhythmias]] including [[ventricular tachycardia]] or [[ventricular fibrillation]] may occur despite [[pacemaker]] placement. Only a few cases of cystic tumor of the AV node has been [[Diagnose|diagnosed]] antemortem. [[Imaging]] modalities including [[echocardiography]] and [[MRI]] are helpful in making the diagnosis. [[Histopathological]] [[examination]] of the [[Resection|resected]] [[tumor]] provides the definitive [[diagnosis]]. Because of the critical location of the [[tumor]] and its unfavorable [[prognosis]], [[Surgery|surgical]] [[excision]] is the mainstay of treatment for cystic tumor of the AV node. [[Anti-arrhythmic medications|Anti-arrhythmic drugs]] and lifelong [[pacemaker]] placement may be necessary after [[excision]] to manage any post-[[Surgery|surgical]] [[AV block]].
 ==Historical Perspective==
-Cystic tumor of the atrioventricular (AV) node was first reported by Armstrong and Mönckeberg in 1911. <ref name="Armstrong">{{cite journal| author= Armstrong H, Mönckeberg JG | title= Herzblock, bedingt durch primären Herztumor, bei einem 5 jährigen Kinde. | journal= Dtsch Arch Klin Med | year= 1911 | volume= 102 | issue=  | pages= 144-146 | }} </ref>
+Cystic tumor of the [[atrioventricular (AV) node]] was first reported by Armstrong and Mönckeberg in 1911. <ref name="Armstrong">{{cite journal| author= Armstrong H, Mönckeberg JG | title= Herzblock, bedingt durch primären Herztumor, bei einem 5 jährigen Kinde. | journal= Dtsch Arch Klin Med | year= 1911 | volume= 102 | issue=  | pages= 144-146 | }} </ref>
 ==Classification==
-There is no established system for the classification of [disease name].
+There is no established system for the [[Cancer staging|staging]] of the cystic tumor of the [[AV node]].
-OR
-There is no established system for the staging of [malignancy name].
-CTAVN are rare. They are choristomatous lesions composed of ectopic gland located in the atrioventricular node and the atrial septum.
-Other midline defects are seen in 10% of the patients.
-Considering their location, congenital heart block is a typical manifestation.
+==Pathophysiology==
+The cystic tumor of the AV node is a [[benign]] [[Congenital disorder|congenital]] [[tumor]]. Although it is also called [[mesothelioma]] of the [[AV node,]] it appears to be a misnomer. The [[origin]] of the cystic tumor of the AV node is still controversial. It is believed that it has [[Endoderm|endodermal]] [[origin]], derived from [[congenital]] rests during [[embryogenesis]]. <ref name="pmid2222148">{{cite journal| author=Burke AP, Anderson PG, Virmani R, James TN, Herrera GA, Ceballos R| title=Tumor of the atrioventricular nodal region. A clinical and immunohistochemical study. | journal=Arch Pathol Lab Med | year= 1990 | volume= 114 | issue= 10 | pages= 1057-62 | pmid=2222148 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=2222148  }} </ref> <ref name="pmid21043810">{{cite journal| author=Cameselle-Teijeiro J, Santías RR, Nallib IA, Forteza J, Barreiro NA| title=Cystic tumor of the atrioventricular node: a rare cardiac pseudoneoplastic lesion. | journal=Arch Pathol Lab Med | year= 2010 | volume= 134 | issue= 11 | pages= 1584-6 | pmid=21043810 | doi=10.1043/2010-0268-LER.1 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=21043810  }} </ref> One study suggested that cystic tumor of the AV node and [[solid]] [[Cell (biology)|cell]] nests of the [[thyroid]] have similar structures and may share the same [[developmental]] process; therefore it is assumed that cystic tumor of the AV node is an [[Ultimobranchial body|ultimobranchial]] [[Heterotopia (medicine)|heterotopia]]. <ref name="pmid15716232">{{cite journal| author=Cameselle-Teijeiro J, Abdulkader I, Soares P, Alfonsín-Barreiro N, Moldes-Boullosa J, Sobrinho-Simões M| title=Cystic tumor of the atrioventricular node of the heart appears to be the heart equivalent of the solid cell nests (ultimobranchial rests) of the thyroid. | journal=Am J Clin Pathol | year= 2005 | volume= 123 | issue= 3 | pages= 369-75 | pmid=15716232 | doi=10.1309/GWT2-PY0T-77PB-BA1A | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=15716232  }} </ref>
-The most common initial manifestation is sudden death.Most CTAVN are diagnosed incidentally at autopsy.
+On [[gross pathology]], small [[multiocular]] [[Cyst|cysts]] are characteristic findings of the cystic tumor of the [[AV node]]. The [[tumor]] may be invisible from the [[endocardial]] surface of the [[heart]]. Therefore, [[Section|sectioning]] through the infero-[[medial]] [[tricuspid]] annulus might be required.  <ref name="pmid26838113">{{cite journal| author=Miller DV| title=Cardiac Tumors. | journal=Surg Pathol Clin | year= 2012 | volume= 5 | issue= 2 | pages= 453-83 | pmid=26838113 | doi=10.1016/j.path.2012.04.007 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=26838113  }} </ref> <ref name="pmid26725181">{{cite journal| author=Burke A, Tavora F| title=The 2015 WHO Classification of Tumors of the Heart and Pericardium. | journal=J Thorac Oncol | year= 2016 | volume= 11 | issue= 4 | pages= 441-52 | pmid=26725181 | doi=10.1016/j.jtho.2015.11.009 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=26725181  }} </ref> The size of the [[tumor]] ranges from 0.5 mm to 30 mm and the size of the [[tumor]] is not correlated with the occurrence of fatal [[arrhythmias]]. <ref name="pmid19237400">{{cite journal |vauthors=Guo J, Zuo S, Lin C, Ji Y |title=Surgical treatment of a giant cystic tumor of the atrioventricular nodal region |journal=Interact Cardiovasc Thorac Surg |volume=8 |issue=5 |pages=592–3 |date=May 2009 |pmid=19237400 |doi=10.1510/icvts.2008.191866 |url=}}</ref>
-There are a few case reports of successfully resected atrioventricular nodal tumors.
+On [[microscopic]] [[histopathological]] [[analysis]], [[solid]] [[cell]] nests and [[cystic]] structures [[Line|lined]] by flattened [[cuboidal]] or [[squamous]] [[epithelium]] mixed with rare [[neuroendocrine cells]] ([[C cells]]) are characteristic findings of the cystic tumor of the AV node. <ref name="pmid26838113">{{cite journal| author=Miller DV| title=Cardiac Tumors. | journal=Surg Pathol Clin | year= 2012 | volume= 5 | issue= 2 | pages= 453-83 | pmid=26838113 | doi=10.1016/j.path.2012.04.007 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=26838113  }} </ref> <ref name="pmid26725181">{{cite journal| author=Burke A, Tavora F| title=The 2015 WHO Classification of Tumors of the Heart and Pericardium. | journal=J Thorac Oncol | year= 2016 | volume= 11 | issue= 4 | pages= 441-52 | pmid=26725181 | doi=10.1016/j.jtho.2015.11.009 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=26725181  }} </ref> <ref name="pmid10722558">{{cite journal| author=Paniagua JR, Sadaba JR, Davidson LA, Munsch CM| title=Cystic tumour of the atrioventricular nodal region: report of a case successfully treated with surgery. | journal=Heart | year= 2000 | volume= 83 | issue= 4 | pages= E6 | pmid=10722558 | doi=10.1136/heart.83.4.e6 | pmc=1729374 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=10722558  }} </ref>
+On [[immunohistochemical staining]], the main [[Tumor cell|tumor cells]] [[stain]] positive for: <ref name="pmid9832064">{{cite journal| author=Arai T, Kurashima C, Wada S, Chida K, Ohkawa S| title=Histological evidence for cell proliferation activity in cystic tumor (endodermal heterotopia) of the atrioventricular node. | journal=Pathol Int | year= 1998 | volume= 48 | issue= 11 | pages= 917-23 | pmid=9832064 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=9832064  }} </ref>
+*[[Cytokeratin]] [[CAM]]5.2
+*[[Cytokeratin]] AE1/AE3
+*[[Cytokeratin]] 34βE12
+*[[Cytokeratin]] 5/6 (CK5/6)
+*[[Cytokeratin]] 7 (CK7)
+*[[Epithelial]] [[membrane]] [[antigen]] (EMA)
+*[[Carcinoembryonic antigen]] ([[CEA]])
+*Carbohydrate antigen ([[CA-19-9|CA]])19.9
+* p63
+*[[bcl2]]
+*[[Galectin-3]]
-==Pathophysiology==
+The [[neuroendocrine cells]] of the [[lesion]] [[stain]] positive for: <ref name="pmid16254122">{{cite journal| author=Evans CA, Suvarna SK| title=Cystic atrioventricular node tumour: not a mesothelioma. | journal=J Clin Pathol | year= 2005 | volume= 58 | issue= 11 | pages= 1232 | pmid=16254122 | doi= | pmc=1770778 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=16254122  }} </ref> <ref name="pmid10722558">{{cite journal| author=Paniagua JR, Sadaba JR, Davidson LA, Munsch CM| title=Cystic tumour of the atrioventricular nodal region: report of a case successfully treated with surgery. | journal=Heart | year= 2000 | volume= 83 | issue= 4 | pages= E6 | pmid=10722558 | doi=10.1136/heart.83.4.e6 | pmc=1729374 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=10722558  }} </ref> <ref name="pmid9832064">{{cite journal| author=Arai T, Kurashima C, Wada S, Chida K, Ohkawa S| title=Histological evidence for cell proliferation activity in cystic tumor (endodermal heterotopia) of the atrioventricular node. | journal=Pathol Int | year= 1998 | volume= 48 | issue= 11 | pages= 917-23 | pmid=9832064 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=9832064  }} </ref>
+*[[CAM|CAM5.2]]
+* Pan-[[keratin]] (AE1/AE3)
+*[[CEA]]
+*[[Calcitonin]]
+*[[Chromogranin]]
+*[[Synaptophysin]]
+* hyroid [[Transcription]] Factor 1 (TTF1)
-[Disease or malignancy name] arises from [cell name]s, which are [cell type] cells that are normally involved in [function of cells].
+The [[tumor]] [[Stain|stains]] negative for: <ref name="pmid16254122">{{cite journal| author=Evans CA, Suvarna SK| title=Cystic atrioventricular node tumour: not a mesothelioma. | journal=J Clin Pathol | year= 2005 | volume= 58 | issue= 11 | pages= 1232 | pmid=16254122 | doi= | pmc=1770778 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=16254122  }} </ref> <ref name="pmid10722558">{{cite journal| author=Paniagua JR, Sadaba JR, Davidson LA, Munsch CM| title=Cystic tumour of the atrioventricular nodal region: report of a case successfully treated with surgery. | journal=Heart | year= 2000 | volume= 83 | issue= 4 | pages= E6 | pmid=10722558 | doi=10.1136/heart.83.4.e6 | pmc=1729374 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=10722558  }} </ref> <ref name="pmid9832064">{{cite journal| author=Arai T, Kurashima C, Wada S, Chida K, Ohkawa S| title=Histological evidence for cell proliferation activity in cystic tumor (endodermal heterotopia) of the atrioventricular node. | journal=Pathol Int | year= 1998 | volume= 48 | issue= 11 | pages= 917-23 | pmid=9832064 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=9832064  }} </ref>
+*[[Keratin]] 20 (CK20)
+*[[p53]]
+*[[Bcl-2]]
+*[[Cyclin D1]]
+*[[Cytokeratin]] 20 (CK20)
+*[[Vimentin]]
+*[[CD31]]
+*[[Factor VIII]] related [[antigen]]
+*[[Estrogen receptor]]
+*[[Progesterone receptor]]
+*[[Thrombomodulin]]
+*[[Wilm's tumor|Wilm’s tumor]] 1
+*[[Calretinin]]
-On gross pathology, small multiocular cysts are characteristic findings of CTAVN.The tumor may be invisible from the endocardial surface of the heart. Therefore, sectioning through the infero-medial tricuspid annulus might be required.<ref name="pmid26838113">{{cite journal| author=Miller DV| title=Cardiac Tumors. | journal=Surg Pathol Clin | year= 2012 | volume= 5 | issue= 2 | pages= 453-83 | pmid=26838113 | doi=10.1016/j.path.2012.04.007 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=26838113  }}</ref> <ref name="pmid26725181">{{cite journal| author=Burke A, Tavora F| title=The 2015 WHO Classification of Tumors of the Heart and Pericardium. | journal=J Thorac Oncol | year= 2016 | volume= 11 | issue= 4 | pages= 441-52 | pmid=26725181 | doi=10.1016/j.jtho.2015.11.009 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=26725181  }} </ref>
+However, true [[mesothelium]] [[Stain|stains]] positive for [[thrombomodulin]], [[Wilm's tumor|Wilm’s tumor]] 1, [[calretinin]] and negative for [[PAS stain|PAS]]. <ref>{{Cite book|title=Diagnostic histopathology of tumors|last=Fletcher|first=Christopher|publisher=Saunders/Elsevier|year=2013|isbn=9781437715347|location=Philadelphia, PA|pages=}}</ref>
-On microscopic histopathological analysis, solid cell nests and cystic structures lined by flattened cuboidal or squamous epithelium mixed with rare neuroendocrine cells are characteristic findings of CTAVN.<nowiki></ref></nowiki> <ref name="pmid26838113">{{cite journal| author=Miller DV| title=Cardiac Tumors. | journal=Surg Pathol Clin | year= 2012 | volume= 5 | issue= 2 | pages= 453-83 | pmid=26838113 | doi=10.1016/j.path.2012.04.007 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=26838113  }} </ref> <ref name="pmid26725181">{{cite journal| author=Burke A, Tavora F| title=The 2015 WHO Classification of Tumors of the Heart and Pericardium. | journal=J Thorac Oncol | year= 2016 | volume= 11 | issue= 4 | pages= 441-52 | pmid=26725181 | doi=10.1016/j.jtho.2015.11.009 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=26725181  }}
+The [[immunohistochemistry staining]] of the cystic tumor of the AV node is in favor of the [[epithelial]] [[differentiation]] of the tumor and supports the labeling of this [[tumor]] as an [[Endoderm|endodermal]] [[Heterotopia (medicine)|heterotopia]]. <ref name="pmid16254122">{{cite journal| author=Evans CA, Suvarna SK| title=Cystic atrioventricular node tumour: not a mesothelioma. | journal=J Clin Pathol | year= 2005 | volume= 58 | issue= 11 | pages= 1232 | pmid=16254122 | doi= | pmc=1770778 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=16254122  }} </ref>
 ==Causes==
-Disease name] may be caused by [cause1], [cause2], or [cause3].
+The cause of the cystic tumor of the AV node has not been identified. Other mid-line [[developmental]] defects are seen in 10% of the patients. <ref name="pmid26725181">{{cite journal| author=Burke A, Tavora F| title=The 2015 WHO Classification of Tumors of the Heart and Pericardium. | journal=J Thorac Oncol | year= 2016 | volume= 11 | issue= 4 | pages= 441-52 | pmid=26725181 | doi=10.1016/j.jtho.2015.11.009 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=26725181  }} </ref>It suggests that a [[genetic]] [[defect]] might involve migration of [[embryological]] [[tissues]] and [[cardiac]] [[neural crest cell]] [[development]] <ref name="pmid15716232">{{cite journal| author=Cameselle-Teijeiro J, Abdulkader I, Soares P, Alfonsín-Barreiro N, Moldes-Boullosa J, Sobrinho-Simões M| title=Cystic tumor of the atrioventricular node of the heart appears to be the heart equivalent of the solid cell nests (ultimobranchial rests) of the thyroid. | journal=Am J Clin Pathol | year= 2005 | volume= 123 | issue= 3 | pages= 369-75 | pmid=15716232 | doi=10.1309/GWT2-PY0T-77PB-BA1A | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=15716232  }} </ref> <ref name="pmid2222148">{{cite journal| author=Burke AP, Anderson PG, Virmani R, James TN, Herrera GA, Ceballos R| title=Tumor of the atrioventricular nodal region. A clinical and immunohistochemical study. | journal=Arch Pathol Lab Med | year= 1990 | volume= 114 | issue= 10 | pages= 1057-62 | pmid=2222148 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=2222148  }} </ref> with possible [[familial]] [[predisposition]]. <ref name="pmid3839372">{{cite journal| author=Travers H| title=Congenital polycystic tumor of the atrioventricular node. | journal=Arch Pathol Lab Med | year= 1985 | volume= 109 | issue= 8 | pages= 704-6 | pmid=3839372 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=3839372  }} </ref> Considering the absence of [[Mitosis|mitoses]] in the [[tumor]], it is suggested to be resulted from a [[dilatation]] of [[cystic]] spaces rather than true [[neoplasm]]. <ref name="pmid6647106">{{cite journal| author=Thorgeirsson G, Liebman J| title=Mesothelioma of the AV node. | journal=Pediatr Cardiol | year= 1983 | volume= 4 | issue= 3 | pages= 219-23 | pmid=6647106 | doi=10.1007/BF02242259 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=6647106  }} </ref> <ref name="pmid10724528">{{cite journal| author=Ford SE| title=Congenital cystic tumors of the atrio-ventricular node: successful demonstration by an abbreviated dissection of the conduction system. | journal=Cardiovasc Pathol | year= 1999 | volume= 8 | issue= 4 | pages= 233-7 | pmid=10724528 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=10724528  }} </ref>
-OR
-Common causes of [disease] include [cause1], [cause2], and [cause3].
-OR
-The most common cause of [disease name] is [cause 1]. Less common causes of [disease name] include [cause 2], [cause 3], and [cause 4].
-OR
-The cause of [disease name] has not been identified. To review risk factors for the development of [disease name], click [[Pericarditis causes#Overview|here]].
-==Differentiating Cystic Tumor of the Atrioventricular Tumor from Other Diseases==
+==Differentiating Cystic Tumor of the AV node from Other Diseases==
-Considering the location and histopathologic <br />
+Cystic tumor of the AV node must be [[Differentiate|differentiated]] from other [[Cardiac tumors differential diagnosis|cardiac tumors]].
 ==Epidemiology and Demographics==
-CTANV is commonly diagnosed in the fourth decade of life. <nowiki><ref name="pmid26725181"></nowiki>{{cite journal| author=Burke A, Tavora F| title=The 2015 WHO Classification of Tumors of the Heart and Pericardium. | journal=J Thorac Oncol | year= 2016 | volume= 11 | issue= 4 | pages= 441-52 | pmid=26725181 | doi=10.1016/j.jtho.2015.11.009 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=26725181  }}</ref>
+[[Primary cardiac neoplasms|Primary cardiac tumors]] are [[rare]] with an [[incidence]] of 0.0017% to 0.03% of all [[Autopsy|autopsies]]. <ref name="pmid26725181">{{cite journal| author=Burke A, Tavora F| title=The 2015 WHO Classification of Tumors of the Heart and Pericardium. | journal=J Thorac Oncol | year= 2016 | volume= 11 | issue= 4 | pages= 441-52 | pmid=26725181 | doi=10.1016/j.jtho.2015.11.009 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=26725181  }} </ref> <ref name="pmid26838113">{{cite journal| author=Miller DV| title=Cardiac Tumors. | journal=Surg Pathol Clin | year= 2012 | volume= 5 | issue= 2 | pages= 453-83 | pmid=26838113 | doi=10.1016/j.path.2012.04.007 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=26838113  }} </ref> Cystic tumor of the AV node accounts for 2.7% of [[cardiac]] [[Tumor|tumors]] and it is the most common [[Primary cardiac neoplasms|primary cardiac tumor]] that causes [[sudden death]]. <ref name="pmid26725181">{{cite journal| author=Burke A, Tavora F| title=The 2015 WHO Classification of Tumors of the Heart and Pericardium. | journal=J Thorac Oncol | year= 2016 | volume= 11 | issue= 4 | pages= 441-52 | pmid=26725181 | doi=10.1016/j.jtho.2015.11.009 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=26725181  }} </ref> <ref name="pmid5897246">{{cite journal| author=Wolf PL, Bing R| title=The smallest tumor which causes sudden death. | journal=JAMA | year= 1965 | volume= 194 | issue= 6 | pages= 674-5 | pmid=5897246 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=5897246  }} </ref>
-The female to male ratio is approximately 3 to 1 <ref name="pmid267251812">{{cite journal| author=Burke A, Tavora F| title=The 2015 WHO Classification of Tumors of the Heart and Pericardium. | journal=J Thorac Oncol | year= 2016 | volume= 11 | issue= 4 | pages= 441-52 | pmid=26725181 | doi=10.1016/j.jtho.2015.11.009 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=26725181  }}</ref>.
-==Risk Factors==
+There is no [[racial]] or [[Ethnic group|ethnic]] [[predilection]] to the cystic tumor of the AV node.
-There are no established risk factors for [disease name].
-OR
+Women are more commonly affected by the cystic tumor of the AV node than men. The female to male [[ratio]] is approximately 3 to 1. <ref name="pmid26838113">{{cite journal| author=Miller DV| title=Cardiac Tumors. | journal=Surg Pathol Clin | year= 2012 | volume= 5 | issue= 2 | pages= 453-83 | pmid=26838113 | doi=10.1016/j.path.2012.04.007 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=26838113  }} </ref>
-The most potent risk factor in the development of [disease name] is [risk factor 1]. Other risk factors include [risk factor 2], [risk factor 3], and [risk factor 4].
+The cystic tumor of the AV node is usually diagnosed in the fourth decade of life. <ref name="pmid26725181">{{cite journal| author=Burke A, Tavora F| title=The 2015 WHO Classification of Tumors of the Heart and Pericardium. | journal=J Thorac Oncol | year= 2016 | volume= 11 | issue= 4 | pages= 441-52 | pmid=26725181 | doi=10.1016/j.jtho.2015.11.009 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=26725181  }} </ref>
-OR
+==Risk Factors==
+There are no established [[risk factor]]<nowiki/>s for the cystic tumor of the AV node.
-Common risk factors in the development of [disease name] include [risk factor 1], [risk factor 2], [risk factor 3], and [risk factor 4].
-OR
-Common risk factors in the development of [disease name] may be occupational, environmental, genetic, and viral.
 ==Screening==
-There is insufficient evidence to recommend routine screening for cystic tumor of the atrioventricular node.
+There is insufficient evidence to recommend routine [[screening]] for the cystic tumor of the AV node.
 ==Natural History, Complications, and Prognosis==
-If left untreated, [#]% of patients with [disease name] may progress to develop [manifestation 1], [manifestation 2], and [manifestation 3].
+Cystic tumor of the AV node is most commonly diagnosed [[postmortem]] in individuals died due to [[sudden cardiac death]]. <ref name="pmid20020153">{{cite journal| author=Patel J, Sheppard MN| title=Cystic tumour of the atrioventricular node: three cases of sudden death. | journal=Int J Legal Med | year= 2011 | volume= 125 | issue= 1 | pages= 139-42 | pmid=20020153 | doi=10.1007/s00414-009-0399-7 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=20020153  }} <ref name="pmid5897246">{{cite journal |vauthors=Wolf PL, Bing R |title=The smallest tumor which causes sudden death |journal=JAMA |volume=194 |issue=6 |pages=674–5 |date=November 1965 |pmid=5897246 |doi= |url=}}</ref> [[Fatal arrhythmias]] including [[ventricular tachycardia]] or [[ventricular fibrillation]] may occur despite [[pacemaker]] placement. <ref name="pmid21056880">{{cite journal| author=Maujean G, Tabib A, Malicier D, Fanton L| title=Sudden death due to a cystic atrio-ventricular node tumour. | journal=J Forensic Leg Med | year= 2010 | volume= 17 | issue= 8 | pages= 437-8 | pmid=21056880 | doi=10.1016/j.jflm.2010.08.009 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=21056880  }} </ref> <ref name="pmid20020153">{{cite journal| author=Patel J, Sheppard MN| title=Cystic tumour of the atrioventricular node: three cases of sudden death. | journal=Int J Legal Med | year= 2011 | volume= 125 | issue= 1 | pages= 139-42 | pmid=20020153 | doi=10.1007/s00414-009-0399-7 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=20020153  }} </ref>
-OR
-Common complications of [disease name] include [complication 1], [complication 2], and [complication 3].
-OR
-Prognosis is generally excellent/good/poor, and the 1/5/10-year mortality/survival rate of patients with [disease name] is approximately [#]%.
 ==Diagnosis==
 ===Diagnostic Study of Choice===
-The diagnosis of [disease name] is made when at least [number] of the following [number] diagnostic criteria are met: [criterion 1], [criterion 2], [criterion 3], and [criterion 4].
+There are no established [[criteria]] for the [[diagnosis]] of cystic tumor of the AV node. Only a few cases of cystic tumor of the AV node has been [[Diagnose|diagnosed]] antemortem. [[Imaging]] modalities including [[echocardiography]] and [[MRI]] are helpful in making the diagnosis. <ref name="pmid25303965">{{cite journal| author=Suzuki K, Matsushita S, Suzuki H, Kuroda K, Inaba H, Arakawa A et al.| title=Cystic tumor of the atrioventricular node: computed tomography and magnetic resonance imaging findings. | journal=J Thorac Imaging | year= 2014 | volume= 29 | issue= 6 | pages= W97-9 | pmid=25303965 | doi=10.1097/RTI.0000000000000111 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=25303965  }} </ref> [[Histopathological]] [[examination]] of the [[Resection|resected]] [[tumor]] provides the definitive [[diagnosis]]. <ref name="pmid25303965">{{cite journal |vauthors=Suzuki K, Matsushita S, Suzuki H, Kuroda K, Inaba H, Arakawa A, Hayashi T, Amano A, Kuwatsuru R |title=Cystic tumor of the atrioventricular node: computed tomography and magnetic resonance imaging findings |journal=J Thorac Imaging |volume=29 |issue=6 |pages=W97–9 |date=November 2014 |pmid=25303965 |doi=10.1097/RTI.0000000000000111 |url=}}</ref>
-OR
-The diagnosis of [disease name] is based on the [criteria name] criteria, which include [criterion 1], [criterion 2], and [criterion 3].
-OR
-The diagnosis of [disease name] is based on the [definition name] definition, which includes [criterion 1], [criterion 2], and [criterion 3].
-OR
-There are no established criteria for the diagnosis of [disease name].
 ===History and Symptoms===
-The majority of patients with [disease name] are asymptomatic.
+The presentation of the cystic tumor of the AV node can range from being [[asymptomatic]] to [[sudden cardiac death]]. <ref name="pmid20020153">{{cite journal| author=Patel J, Sheppard MN| title=Cystic tumour of the atrioventricular node: three cases of sudden death. | journal=Int J Legal Med | year= 2011 | volume= 125 | issue= 1 | pages= 139-42 | pmid=20020153 | doi=10.1007/s00414-009-0399-7 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=20020153  }} </ref><ref name="pmid25303965">{{cite journal |vauthors=Suzuki K, Matsushita S, Suzuki H, Kuroda K, Inaba H, Arakawa A, Hayashi T, Amano A, Kuwatsuru R |title=Cystic tumor of the atrioventricular node: computed tomography and magnetic resonance imaging findings |journal=J Thorac Imaging |volume=29 |issue=6 |pages=W97–9 |date=November 2014 |pmid=25303965 |doi=10.1097/RTI.0000000000000111 |url=}}</ref>
+Typical [[Symptom|symptoms]] are: <ref name="pmid10722558">{{cite journal| author=Paniagua JR, Sadaba JR, Davidson LA, Munsch CM| title=Cystic tumour of the atrioventricular nodal region: report of a case successfully treated with surgery. | journal=Heart | year= 2000 | volume= 83 | issue= 4 | pages= E6 | pmid=10722558 | doi=10.1136/heart.83.4.e6 | pmc=1729374 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=10722558  }} </ref> <ref name="pmid28438795">{{cite journal |vauthors=Abuzeid W, Myers RBH |title=Cystic tumour of the atrioventricular node: treatment dilemma |journal=BMJ Case Rep |volume=2017 |issue= |pages= |date=April 2017 |pmid=28438795 |pmc=5534749 |doi=10.1136/bcr-2017-219314 |url=}}</ref><ref name="pmid21820324">{{cite journal| author=Law KB, Feng T, Nair V, Cusimano RJ, Butany J| title=Cystic tumor of the atrioventricular node: rare antemortem diagnosis. | journal=Cardiovasc Pathol | year= 2012 | volume= 21 | issue= 2 | pages= 120-7 | pmid=21820324 | doi=10.1016/j.carpath.2011.05.004 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=21820324  }} </ref> <ref name="pmid5016834">{{cite journal| author=Lewman LV, Demany MA, Zimmerman HA| title=Congenital tumor of atrioventricular node with complete heart block and sudden death. Mesothelioma or lymphangio-endothelioma of atrioventricular node. | journal=Am J Cardiol | year= 1972 | volume= 29 | issue= 4 | pages= 554-7 | pmid=5016834 | doi=10.1016/0002-9149(72)90448-1 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=5016834  }} </ref>
+*[[Palpitations]]
+*[[Dyspnea]]
+*[[syncope]]
+*[[Dizziness]]
-OR
+Patients may also present with partial or [[complete heart block]]. <ref name="pmid21820324">{{cite journal| author=Law KB, Feng T, Nair V, Cusimano RJ, Butany J| title=Cystic tumor of the atrioventricular node: rare antemortem diagnosis. | journal=Cardiovasc Pathol | year= 2012 | volume= 21 | issue= 2 | pages= 120-7 | pmid=21820324 | doi=10.1016/j.carpath.2011.05.004 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=21820324  }} </ref> <ref name="pmid5124984">{{cite journal| author=Hopkinson JM, Newcombe CP| title=Heart block due to epithelial heterotopia. | journal=J Pathol | year= 1971 | volume= 104 | issue= 3 | pages= 218-20 | pmid=5124984 | doi=10.1002/path.1711040312 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=5124984  }} </ref> <ref name="pmid21056880">{{cite journal| author=Maujean G, Tabib A, Malicier D, Fanton L| title=Sudden death due to a cystic atrio-ventricular node tumour. | journal=J Forensic Leg Med | year= 2010 | volume= 17 | issue= 8 | pages= 437-8 | pmid=21056880 | doi=10.1016/j.jflm.2010.08.009 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=21056880  }} </ref>
-The hallmark of [disease name] is [finding]. A positive history of [finding 1] and [finding 2] is suggestive of [disease name]. The most common symptoms of [disease name] include [symptom 1], [symptom 2], and [symptom 3]. Common symptoms of [disease] include [symptom 1], [symptom 2], and [symptom 3]. Less common symptoms of [disease name] include [symptom 1], [symptom 2], and [symptom 3].
 ===Physical Examination===
-Patients with [disease name] usually appear [general appearance]. Physical examination of patients with [disease name] is usually remarkable for [finding 1], [finding 2], and [finding 3].
+[[Physical examination]] of [[Patient|patients]] with cystic tumor of the AV node is usually unremarkable.
-OR
-Common physical examination findings of [disease name] include [finding 1], [finding 2], and [finding 3].
-OR
-The presence of [finding(s)] on physical examination is diagnostic of [disease name].
-OR
-The presence of [finding(s)] on physical examination is highly suggestive of [disease name].
 ===Laboratory Findings===
+There are no [[Diagnosis|diagnostic]] [[laboratory]] findings associated with cystic tumor of the AV node.
-The cysts contain a clear to mucoid material and mucinous, ciliated, goblet and transitional type cells may also be present in the lining (Fig. 29). The cells express CK7, but not CK20, and also stain positive for EMA and CEA. Miller
 ===Electrocardiogram===
-There are no ECG findings associated with [disease name].
+An [[ECG]] may be helpful in the [[diagnosis]] of cystic tumor of the AV node. [[ECG]] might show partial or [[complete heart block]]. <ref name="pmid21820324">{{cite journal| author=Law KB, Feng T, Nair V, Cusimano RJ, Butany J| title=Cystic tumor of the atrioventricular node: rare antemortem diagnosis. | journal=Cardiovasc Pathol | year= 2012 | volume= 21 | issue= 2 | pages= 120-7 | pmid=21820324 | doi=10.1016/j.carpath.2011.05.004 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=21820324  }} </ref><ref name="pmid28438795">{{cite journal| author=Abuzeid W, Myers RBH| title=Cystic tumour of the atrioventricular node: treatment dilemma. | journal=BMJ Case Rep | year= 2017 | volume= 2017 | issue=  | pages=  | pmid=28438795 | doi=10.1136/bcr-2017-219314 | pmc=5534749 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=28438795  }} </ref><ref name="pmid24182482">{{cite journal| author=Careddu L, Pantaleo A, Savini C, Di Eusanio M, Leone O, Di Bartolomeo R| title=Cystic atrioventricular node tumor excision by minimally invasive surgery. | journal=Ann Thorac Surg | year= 2013 | volume= 96 | issue= 5 | pages= 1873-5 | pmid=24182482 | doi=10.1016/j.athoracsur.2013.03.036 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=24182482  }} </ref>
-OR
-An ECG may be helpful in the diagnosis of [disease name]. Findings on an ECG suggestive of/diagnostic of [disease name] include [finding 1], [finding 2], and [finding 3].
 ===X-ray===
-There are no x-ray findings associated with cystic tumor of the atrioventricular tumor.
+There are no [[x-ray]] findings associated with cystic tumor of the AV node.
 ===Echocardiography or Ultrasound===
-There are no echocardiography/ultrasound  findings associated with [disease name].
+[[Echocardiography]] may be helpful in the [[diagnosis]] of cystic tumor of the AV node, showing a [[mass]] at the site of the tumor. <ref name="pmid28438795">{{cite journal| author=Abuzeid W, Myers RBH| title=Cystic tumour of the atrioventricular node: treatment dilemma. | journal=BMJ Case Rep | year= 2017 | volume= 2017 | issue=  | pages=  | pmid=28438795 | doi=10.1136/bcr-2017-219314 | pmc=5534749 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=28438795  }} </ref> <ref name="pmid21820324">{{cite journal| author=Law KB, Feng T, Nair V, Cusimano RJ, Butany J| title=Cystic tumor of the atrioventricular node: rare antemortem diagnosis. | journal=Cardiovasc Pathol | year= 2012 | volume= 21 | issue= 2 | pages= 120-7 | pmid=21820324 | doi=10.1016/j.carpath.2011.05.004 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=21820324  }} </ref> <ref name="pmid24182482">{{cite journal| author=Careddu L, Pantaleo A, Savini C, Di Eusanio M, Leone O, Di Bartolomeo R| title=Cystic atrioventricular node tumor excision by minimally invasive surgery. | journal=Ann Thorac Surg | year= 2013 | volume= 96 | issue= 5 | pages= 1873-5 | pmid=24182482 | doi=10.1016/j.athoracsur.2013.03.036 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=24182482  }} </ref>
-OR
-Echocardiography/ultrasound  may be helpful in the diagnosis of [disease name]. Findings on an echocardiography/ultrasound suggestive of/diagnostic of [disease name] include [finding 1], [finding 2], and [finding 3].
-OR
-There are no echocardiography/ultrasound  findings associated with [disease name]. However, an echocardiography/ultrasound  may be helpful in the diagnosis of complications of [disease name], which include [complication 1], [complication 2], and [complication 3].
 ===CT scan===
-There are no CT scan findings associated with cystic tumor of the atrioventricular tumor.
+Only a few cases of cystic tumor of the AV node have been reported antemortem. Therefore, the data regarding the [[imaging]] findings are limited. Reports have shown either a high-[[attenuation]] <ref name="pmid16195634">{{cite journal| author=Saito S, Kobayashi J, Tagusari O, Bando K, Niwaya K, Nakajima H et al.| title=Successful excision of a cystic tumor of the atrioventricular nodal region. | journal=Circ J | year= 2005 | volume= 69 | issue= 10 | pages= 1293-4 | pmid=16195634 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=16195634  }} </ref> or low-attenuation [[Lesion|lesions]] on [[Computed tomography|CT]] [[images]]. <ref name="Kaminishi">{{cite journal| author= Kaminishi Y, Watanabe Y, Nakata H, et al. | title= Cystic tumor of the atrioventricular nodal region. | journal= . Jpn J Thorac Cardiovasc Surg. | year= 2002 | volume= 50 | issue=  | pages= 37-39 | }} </ref>
 ===MRI===
-There are no MRI findings associated with [disease name].
+[[Cardiac MRI]] may be helpful in the [[diagnosis]] of the cystic tumor of the AV node. High-signal [[intensity]] lesion on T1-weighted <ref name="pmid10722558">{{cite journal| author=Paniagua JR, Sadaba JR, Davidson LA, Munsch CM| title=Cystic tumour of the atrioventricular nodal region: report of a case successfully treated with surgery. | journal=Heart | year= 2000 | volume= 83 | issue= 4 | pages= E6 | pmid=10722558 | doi=10.1136/heart.83.4.e6 | pmc=1729374 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=10722558  }} </ref> <ref name="pmid16195634">{{cite journal| author=Saito S, Kobayashi J, Tagusari O, Bando K, Niwaya K, Nakajima H et al.| title=Successful excision of a cystic tumor of the atrioventricular nodal region. | journal=Circ J | year= 2005 | volume= 69 | issue= 10 | pages= 1293-4 | pmid=16195634 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=16195634  }} </ref> <ref name="pmid25303965">{{cite journal| author=Suzuki K, Matsushita S, Suzuki H, Kuroda K, Inaba H, Arakawa A et al.| title=Cystic tumor of the atrioventricular node: computed tomography and magnetic resonance imaging findings. | journal=J Thorac Imaging | year= 2014 | volume= 29 | issue= 6 | pages= W97-9 | pmid=25303965 | doi=10.1097/RTI.0000000000000111 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=25303965  }} </ref>and T2-weighted [[MRI]] <ref name="pmid16195634">{{cite journal| author=Saito S, Kobayashi J, Tagusari O, Bando K, Niwaya K, Nakajima H et al.| title=Successful excision of a cystic tumor of the atrioventricular nodal region. | journal=Circ J | year= 2005 | volume= 69 | issue= 10 | pages= 1293-4 | pmid=16195634 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=16195634  }} </ref> or low signal intensity on T2-weighted MRI <ref name="pmid25303965">{{cite journal| author=Suzuki K, Matsushita S, Suzuki H, Kuroda K, Inaba H, Arakawa A et al.| title=Cystic tumor of the atrioventricular node: computed tomography and magnetic resonance imaging findings. | journal=J Thorac Imaging | year= 2014 | volume= 29 | issue= 6 | pages= W97-9 | pmid=25303965 | doi=10.1097/RTI.0000000000000111 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=25303965  }} </ref> have been reported.
-OR
-[Location] MRI may be helpful in the diagnosis of [disease name]. Findings on MRI suggestive of/diagnostic of [disease name] include [finding 1], [finding 2], and [finding 3].
-OR
-There are no MRI findings associated with [disease name]. However, a MRI may be helpful in the diagnosis of complications of [disease name], which include [complication 1], [complication 2], and [complication 3].
 ===Other Imaging Findings===
-There are no other imaging findings associated with cystic tumor of the atrioventricular tumor.
+There are no other [[imaging]] findings associated with cystic tumor of the AV node.
 ===Other Diagnostic Studies===
-There are no other diagnostic studies associated with cystic tumor of the atrioventricular tumor.
+There are no other [[diagnostic]] studies associated with cystic tumor of the AV node.
 ==Treatment==
 ===Medical Therapy===
+There is no [[medical]] treatment for the cystic tumor of the AV node.
-There is no medical treatment for cystic tumor of the atrioventricular tumor.
 ===Surgery===
-Because of the critical location of the tumor and its unfavorable prognosis, surgical excision is the mainstay of treatment for cystic tumor of the atrioventricular node. Anti-arrhythmic drugs and lifelong pacemaker placement may be necessary after excision to manage any post-surgical AV block. <ref name="pmid26838113" /> <ref name="pmid29221317">{{cite journal| author=Luc JGY, Phan K, Tchantchaleishvili V| title=Cystic tumor of the atrioventricular node: a review of the literature. | journal=J Thorac Dis | year= 2017 | volume= 9 | issue= 9 | pages= 3313-3318 | pmid=29221317 | doi=10.21037/jtd.2017.08.101 | pmc=5708412 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=29221317  }} </ref>
+Because of the critical location of the [[tumor]] and its unfavorable [[prognosis]], [[Surgery|surgical]] [[excision]] is the mainstay of treatment for cystic tumor of the AV node. [[Anti-arrhythmic medications|Anti-arrhythmic drugs]] and lifelong [[pacemaker]] placement may be necessary after [[excision]] to manage any post-surgical [[AV block]]. <ref name="pmid26838113">{{cite journal| author=Miller DV| title=Cardiac Tumors. | journal=Surg Pathol Clin | year= 2012 | volume= 5 | issue= 2 | pages= 453-83 | pmid=26838113 | doi=10.1016/j.path.2012.04.007 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=26838113  }} </ref> <ref name="pmid26725181">{{cite journal| author=Burke A, Tavora F| title=The 2015 WHO Classification of Tumors of the Heart and Pericardium. | journal=J Thorac Oncol | year= 2016 | volume= 11 | issue= 4 | pages= 441-52 | pmid=26725181 | doi=10.1016/j.jtho.2015.11.009 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=26725181  }} </ref>
-<br />
 ===Primary Prevention===
-There are no established measures for the primary prevention of cystic tumor of the atrioventricular tumor.
+There are no established measures for the [[primary prevention]] of the cystic tumor of the AV node.
 ===Secondary Prevention===
-There are no established measures for the secondary prevention of cystic tumor of the atrioventricular node.
+There are no established measures for the [[secondary prevention]] of the cystic tumor of the AV node.
 ==References==