Ganglioneuroma overview: Difference between revisions
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==Overview== | ==Overview== | ||
Ganglioneuroma is a rare and benign tumor of the peripheral nervous system that tends to affect children and young adults.<ref>Introduction of ganglioneuroma. National Library of Medicine. https://www.nlm.nih.gov/medlineplus/ency/article/001437.htm</ref> Ganglioneuroma may be classified into two subtypes/groups: Ganglioneuroma-maturing and ganglioneuroma-mature.<ref name="pmid19530234">{{cite journal| author=Okamatsu C, London WB, Naranjo A, Hogarty MD, Gastier-Foster JM, Look AT et al.| title=Clinicopathological characteristics of ganglioneuroma and ganglioneuroblastoma: a report from the CCG and COG. | journal=Pediatr Blood Cancer | year= 2009 | volume= 53 | issue= 4 | pages= 563-9 | pmid=19530234 | doi=10.1002/pbc.22106 | pmc=PMC2730988 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=19530234 }} </ref> Ganglioneuromas are derived from the primordial [[neural crest cells]], which are undifferentiated cells of the [[sympathetic nervous system]]. On gross pathology, ganglioneuromas are characterized by solid, white, firm, well-circumscribed, and nodular tumors. On microscopic histopathological analysis, ganglioneuromas are characterized by spindle-shaped cells with cell borders in a fibrillar matrix containing [[ganglion cells]] with large round [[nuclei]], prominent [[nucleoli]], and abundant [[eosinophilic]] cytoplasm.<ref name="pmid22907039">{{cite journal| author=Vasiliadis K, Papavasiliou C, Fachiridis D, Pervana S, Michaelides M, Kiranou M et al.| title=Retroperitoneal extra-adrenal ganglioneuroma involving the infrahepatic inferior vena cava, celiac axis and superior mesenteric artery: A case report. | journal=Int J Surg Case Rep | year= 2012 | volume= 3 | issue= 11 | pages= 541-3 | pmid=22907039 | doi=10.1016/j.ijscr.2012.07.008 | pmc=PMC3437388 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22907039 }} </ref> Ganglioglioma must be differentiated from [[neuroblastoma]], ganglioneuroblastoma, spinal [[schwannoma]], spinal [[neurofibroma]], [[adrenal adenoma]], [[adrenal carcinoma]], and [[pheochromocytoma]].<ref name=ddd>D.Dx of ganglioneuroma. Dr Bruno Di Muzio and Dr Yuranga Weerakkody et al. Radiopaedia 2015. http://radiopaedia.org/articles/ganglioneuroma</ref><ref name=staging>{{cite journal |last=Adam |first=O |last2=Boia |first2=ES |date=2007 |title=ganglioneuroma |url=http://www.jurnalulpediatrului.ro/pages/arhiva/39-40/39-40-IV-11.pdf |journal=jurnalul pediatrului |publisher= |volume=10 |issue=39-40|doi= |access-date=10 September 2015}}</ref> Females are more commonly affected with ganglioneuroma than males.<ref name=staging>{{cite journal |last=Adam |first=O |last2=Boia |first2=ES |date=2007 |title=ganglioneuroma |url=http://www.jurnalulpediatrului.ro/pages/arhiva/39-40/39-40-IV-11.pdf |journal=jurnalul pediatrului |publisher= |volume=10 |issue=39-40|doi= |access-date=10 September 2015}}</ref> Common complications of ganglioneuroma include [[paralysis]], [[metastases]], and local recurrence.<ref>Complications of ganglioneuroma. National Library of Medicine. https://www.nlm.nih.gov/medlineplus/ency/article/001437.htm</ref> The prognosis of ganglioneuroma is excellent with treatment.<ref name=ddd>Prognosis of ganglioneuroma. Dr Bruno Di Muzio and Dr Yuranga Weerakkody et al. Radiopaedia 2015. http://radiopaedia.org/articles/ganglioneuroma</ref> Symptoms of ganglioneuroma include [[dyspnea]], [[chest pain]], [[abdominal pain]], [[bloating]], pain and [[numbness]] in limbs, [[paresis]], [[diarrhea]], [[diaphoresis]], and [[hirsuitism]].<ref name=ddd>Symptoms of ganglioneuroma. National Library of Medicine. https://www.nlm.nih.gov/medlineplus/ency/article/001437.htm</ref> Common physical examination findings of ganglioneuroma include [[dyspnea]], [[stridor]], motor loss, [[sensory loss]], [[diaphoresis]], [[scoliosis]], [[clitoromegaly]], [[hirsuitism]], and [[hypertension]].<ref name=ddd>Signs of ganglioneuroma. National Library of Medicine. https://www.nlm.nih.gov/medlineplus/ency/article/001437.htm</ref> On chest x-ray, ganglioneuroma is characterized by a posterior [[mediastinal mass]], which may cause [[rib]] spreading and foraminal erosion.<ref name=ddd>X ray findings of ganglioneuroma. Dr Bruno Di Muzio and Dr Yuranga Weerakkody et al. Radiopaedia 2015. http://radiopaedia.org/articles/ganglioneuroma</ref> On CT scan, ganglioneuroma is characterized by a solid, well-circumscribed, and encapsulated mass that is iso to hypoattenuating to muscle.<ref name=ddd>CT findings of ganglioneuroma. Dr Bruno Di Muzio and Dr Yuranga Weerakkody et al. Radiopaedia 2015. http://radiopaedia.org/articles/ganglioneuroma</ref><ref name=staging>{{cite journal |last=Adam |first=O |last2=Boia |first2=ES |date=2007 |title=ganglioneuroma |url=http://www.jurnalulpediatrului.ro/pages/arhiva/39-40/39-40-IV-11.pdf |journal=jurnalul pediatrului |publisher= |volume=10 |issue=39-40|doi= |access-date=10 September 2015}}</ref> On MRI scan, ganglioneuroma is characterized by a well circumscribed and encapsulatated mass with low signal intensity on T1-weighted images and intermediate to high signal intensity on T2-weighted images. [[Surgery]] is the mainstay of treatment for symptomatic ganglioneuroma. Adjunctive [[chemotherapy]] and [[radiotherapy]] may be required.<ref name=ddd>Rx of ganglioneuroma. Dr Bruno Di Muzio and Dr Yuranga Weerakkody et al. Radiopaedia 2015. http://radiopaedia.org/articles/ganglioneuroma</ref> | |||
==Classification== | ==Classification== | ||
According to International Neuroblastoma Pathology Classification (INPC), ganglioneuroma may be classified into two | According to International Neuroblastoma Pathology Classification (INPC), ganglioneuroma may be classified into two groups: Ganglioneuroma-maturing and ganglioneuroma-mature.<ref name="pmid19530234">{{cite journal| author=Okamatsu C, London WB, Naranjo A, Hogarty MD, Gastier-Foster JM, Look AT et al.| title=Clinicopathological characteristics of ganglioneuroma and ganglioneuroblastoma: a report from the CCG and COG. | journal=Pediatr Blood Cancer | year= 2009 | volume= 53 | issue= 4 | pages= 563-9 | pmid=19530234 | doi=10.1002/pbc.22106 | pmc=PMC2730988 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=19530234 }} </ref> | ||
==Pathophysiology== | ==Pathophysiology== | ||
On gross pathology, ganglioneuromas are characterized by solid, white, firm, well-circumscribed, and nodular tumors. On microscopic histopathological analysis, ganglioneuromas are characterized by spindle-shaped cells with cell borders in a fibrillar matrix containing [[ganglion cells]] with large round [[nuclei]], prominent [[nucleoli]], and abundant [[eosinophilic]] cytoplasm.<ref name="pmid22907039">{{cite journal| author=Vasiliadis K, Papavasiliou C, Fachiridis D, Pervana S, Michaelides M, Kiranou M et al.| title=Retroperitoneal extra-adrenal ganglioneuroma involving the infrahepatic inferior vena cava, celiac axis and superior mesenteric artery: A case report. | journal=Int J Surg Case Rep | year= 2012 | volume= 3 | issue= 11 | pages= 541-3 | pmid=22907039 | doi=10.1016/j.ijscr.2012.07.008 | pmc=PMC3437388 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22907039 }} </ref> | Ganglioneuromas are derived from the primordial [[neural crest cells]], which are undifferentiated cells of the [[sympathetic nervous system]]. Genes involved in the pathogenesis of ganglioneuroma include ''MYCN'' [[oncogene]] and chromosome 1p36. On gross pathology, ganglioneuromas are characterized by solid, white, firm, well-circumscribed, and nodular tumors. On microscopic histopathological analysis, ganglioneuromas are characterized by spindle-shaped cells with cell borders in a fibrillar matrix containing [[ganglion cells]] with large round [[nuclei]], prominent [[nucleoli]], and abundant [[eosinophilic]] cytoplasm.<ref name="pmid22907039">{{cite journal| author=Vasiliadis K, Papavasiliou C, Fachiridis D, Pervana S, Michaelides M, Kiranou M et al.| title=Retroperitoneal extra-adrenal ganglioneuroma involving the infrahepatic inferior vena cava, celiac axis and superior mesenteric artery: A case report. | journal=Int J Surg Case Rep | year= 2012 | volume= 3 | issue= 11 | pages= 541-3 | pmid=22907039 | doi=10.1016/j.ijscr.2012.07.008 | pmc=PMC3437388 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22907039 }} </ref> | ||
==Causes== | ==Causes== | ||
| Line 15: | Line 16: | ||
==Differentiating brain tumors from other diseases== | ==Differentiating brain tumors from other diseases== | ||
Ganglioglioma must be differentiated from [[neuroblastoma]], ganglioneuroblastoma, spinal [[schwannoma]], spinal [[neurofibroma]], [[adrenal adenoma]], [[adrenal carcinoma]], and [[pheochromocytoma]].<ref name=ddd>D.Dx of ganglioneuroma. Dr Bruno Di Muzio and Dr Yuranga Weerakkody et al. Radiopaedia 2015. http://radiopaedia.org/articles/ganglioneuroma</ref><ref name=staging>{{cite journal |last=Adam |first=O |last2=Boia |first2=ES |date=2007 |title=ganglioneuroma |url=http://www.jurnalulpediatrului.ro/pages/arhiva/39-40/39-40-IV-11.pdf |journal=jurnalul pediatrului |publisher= |volume=10 |issue=39-40|doi= |access-date=10 September 2015}}</ref> | |||
==Epidemiology and Demographics== | ==Epidemiology and Demographics== | ||
The [[incidence]] of ganglioneuroma is approximately 1 per 100,000 children in the United States.<ref name=staging>{{cite journal |last=Adam |first=O |last2=Boia |first2=ES |date=2007 |title=ganglioneuroma |url=http://www.jurnalulpediatrului.ro/pages/arhiva/39-40/39-40-IV-11.pdf |journal=jurnalul pediatrului |publisher= |volume=10 |issue=39-40|doi= |access-date=10 September 2015}}</ref> Ganglioneuroma is a rare disease that tends to affect children and young adults.<ref name=ddd>Epidemiology of ganglioneuroma. Dr Bruno Di Muzio and Dr Yuranga Weerakkody et al. Radiopaedia 2015. http://radiopaedia.org/articles/ganglioneuroma</ref> Females are more commonly affected with ganglioneuroma than males.<ref name=staging>{{cite journal |last=Adam |first=O |last2=Boia |first2=ES |date=2007 |title=ganglioneuroma |url=http://www.jurnalulpediatrului.ro/pages/arhiva/39-40/39-40-IV-11.pdf |journal=jurnalul pediatrului |publisher= |volume=10 |issue=39-40|doi= |access-date=10 September 2015}}</ref> There is no racial predilection to ganglioneuroma. | |||
==Risk factors== | ==Risk factors== | ||
There are no established risk factors for ganglioneuroma.<ref name=ddd>Risk factors for ganglioneuroma. National Library of Meidicine. https://www.nlm.nih.gov/medlineplus/ency/article/001437.htm</ref> | |||
==Screening== | |||
Screening for ganglioneuroma is not recommended.<ref name="pmid22978818">{{cite journal| author=Fiori E, Pozzessere C, Lamazza A, Leone G, Borrini F, Schillaci A et al.| title=Endoscopic treatment of ganglioneuroma of the colon associated with a lipoma: a case report. | journal=J Med Case Rep | year= 2012 | volume= 6 | issue= | pages= 304 | pmid=22978818 | doi=10.1186/1752-1947-6-304 | pmc=PMC3469395 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=22978818 }} </ref> | |||
==Natural History, Complications and Prognosis== | ==Natural History, Complications and Prognosis== | ||
Common complications of ganglioneuroma include [[paralysis]], [[metastases]], and local recurrence.<ref>Complications of ganglioneuroma. National Library of Medicine. https://www.nlm.nih.gov/medlineplus/ency/article/001437.htm</ref> The prognosis of ganglioneuroma is excellent with treatment.<ref name=ddd>Prognosis of ganglioneuroma. Dr Bruno Di Muzio and Dr Yuranga Weerakkody et al. Radiopaedia 2015. http://radiopaedia.org/articles/ganglioneuroma</ref> | |||
== | ==Staging== | ||
According to the International Neuroblastoma Staging System (INSS), there are six stages of ganglioneuroma based on [[clinical]], radiologic, and [[surgical]] features.<ref name=staging>{{cite journal |last=Adam |first=O |last2=Boia |first2=ES |date=2007 |title=ganglioneuroma |url=http://www.jurnalulpediatrului.ro/pages/arhiva/39-40/39-40-IV-11.pdf |journal=jurnalul pediatrului |publisher= |volume=10 |issue=39-40|doi= |access-date=10 September 2015}}</ref> | |||
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== | ==History and Symptoms== | ||
Symptoms of ganglioneuroma include [[dyspnea]], [[chest pain]], [[abdominal pain]], [[bloating]], pain and [[numbness]] in limbs, [[paresis]], [[diarrhea]], [[diaphoresis]], and [[hirsuitism]].<ref name=ddd>Symptoms of ganglioneuroma. National Library of Medicine. https://www.nlm.nih.gov/medlineplus/ency/article/001437.htm</ref> | |||
== | ==Physical examination== | ||
Common physical examination findings of ganglioneuroma include [[dyspnea]], [[stridor]], motor loss, [[sensory loss]], [[diaphoresis]], [[scoliosis]], [[clitoromegaly]], [[hirsuitism]], and [[hypertension]].<ref name=ddd>Signs of ganglioneuroma. National Library of Medicine. https://www.nlm.nih.gov/medlineplus/ency/article/001437.htm</ref> | |||
=== | ==Laboratory Findings== | ||
Some patients with ganglioneuroma may have elevated concentrations of [[VMA]] ([[vanillylmandelic acid]]) or HVA ([[homovanillic acid]]) in urine.<ref name=ddd>.Laboratory findings of ganglioneuroma. Carmen Perrino, M.D. & Debra Zynger, M.D. Pathology Outlines. http://www.pathologyoutlines.com/topic/adrenalganglioneuroma.html</ref><ref name=staging>{{cite journal |last=Adam |first=O |last2=Boia |first2=ES |date=2007 |title=ganglioneuroma |url=http://www.jurnalulpediatrului.ro/pages/arhiva/39-40/39-40-IV-11.pdf |journal=jurnalul pediatrului |publisher= |volume=10 |issue=39-40|doi= |access-date=10 September 2015}}</ref> | |||
== | ==X Ray== | ||
On chest x-ray, ganglioneuroma is characterized by a posterior [[mediastinal mass]], which may cause [[rib]] spreading and foraminal erosion. Plain x-rays may show a mass in the [[retroperitoneum]], [[pelvis]], or neck indicating the presence of [[metastasis]].<ref name=ddd>X ray findings of ganglioneuroma. Dr Bruno Di Muzio and Dr Yuranga Weerakkody et al. Radiopaedia 2015. http://radiopaedia.org/articles/ganglioneuroma</ref> | |||
=== | ==CT== | ||
Chest, abdomen, and pelvic CT scan may be helpful in the diagnosis of ganglioneuroma. Findings on CT scan suggestive of ganglioneuroma include a solid, well-circumscribed, and encapsulated mass that is iso to hypoattenuating to muscle.<ref name=ddd>CT findings of ganglioneuroma. Dr Bruno Di Muzio and Dr Yuranga Weerakkody et al. Radiopaedia 2015. http://radiopaedia.org/articles/ganglioneuroma</ref><ref name=staging>{{cite journal |last=Adam |first=O |last2=Boia |first2=ES |date=2007 |title=ganglioneuroma |url=http://www.jurnalulpediatrului.ro/pages/arhiva/39-40/39-40-IV-11.pdf |journal=jurnalul pediatrului |publisher= |volume=10 |issue=39-40|doi= |access-date=10 September 2015}}</ref> | |||
== | ==MRI== | ||
Chest and abdominal MRI scan may be helpful in the diagnosis of ganglioneuroma. On MRI scan, ganglioneuroma is characterized by a well circumscribed and encapsulatated mass with low signal intensity on T1-weighted images and intermediate to high signal intensity on T2-weighted images.<ref name=ddd>MRI findings for ganglioneuroma. Dr Bruno Di Muzio and Dr Yuranga Weerakkody et al. Radiopaedia 2015. http://radiopaedia.org/articles/ganglioneuroma</ref> | |||
== | ==Ultrasound== | ||
=== | On ultrasound, ganglioneuroma is characterized by a homogeneous, hypoechoic, well circumscribed mass.<ref name=staging>{{cite journal |last=Adam |first=O |last2=Boia |first2=ES |date=2007 |title=ganglioneuroma |url=http://www.jurnalulpediatrului.ro/pages/arhiva/39-40/39-40-IV-11.pdf |journal=jurnalul pediatrului |publisher= |volume=10 |issue=39-40|doi= |access-date=10 September 2015}}</ref> | ||
=== | ==Other Imaging Findings== | ||
Other imaging tests for ganglioneuroma include [[scintigraphy]] or medaiodobenzylguanidine (MIBG) scan.<ref name=staging>{{cite journal |last=Adam |first=O |last2=Boia |first2=ES |date=2007 |title=ganglioneuroma |url=http://www.jurnalulpediatrului.ro/pages/arhiva/39-40/39-40-IV-11.pdf |journal=jurnalul pediatrului |publisher= |volume=10 |issue=39-40|doi= |access-date=10 September 2015}}</ref> | |||
==Other Diagnostic Studies== | |||
Other diagnostic studies for ganglioneuroma include [[biopsy]], which demonstrates spindle-shaped cells with cell borders in a fibrillar matrix containing [[ganglion cells]] with large round [[nuclei]], prominent [[nucleoli]], and abundant [[eosinophilic]] cytoplasm.<ref name=ddd>Diagnosis of ganglioneuroma. National Library of Medicine. https://www.nlm.nih.gov/medlineplus/ency/article/001437.htm</ref> | |||
==Medical Therapy== | |||
The predominant therapy for symptomatic ganglioneuroma is [[surgical resection]]. Adjunctive [[chemotherapy]] and [[radiotherapy]] may be required.<ref name=ddd>Rx of ganglioneuroma. Dr Bruno Di Muzio and Dr Yuranga Weerakkody et al. Radiopaedia 2015. http://radiopaedia.org/articles/ganglioneuroma</ref> | |||
==Surgery== | |||
Surgery is the mainstay of treatment for symptomatic ganglioneuroma.<ref name=ddd>Treatment of ganglioneuroma. Dr Bruno Di Muzio and Dr Yuranga Weerakkody et al. Radiopaedia 2015. http://radiopaedia.org/articles/ganglioneuroma</ref> | |||
== References == | ==References== | ||
{{reflist|2}} | {{reflist|2}} | ||
Latest revision as of 17:44, 15 September 2015
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Ganglioneuroma Microchapters |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Sujit Routray, M.D. [2]
Overview
Ganglioneuroma is a rare and benign tumor of the peripheral nervous system that tends to affect children and young adults.[1] Ganglioneuroma may be classified into two subtypes/groups: Ganglioneuroma-maturing and ganglioneuroma-mature.[2] Ganglioneuromas are derived from the primordial neural crest cells, which are undifferentiated cells of the sympathetic nervous system. On gross pathology, ganglioneuromas are characterized by solid, white, firm, well-circumscribed, and nodular tumors. On microscopic histopathological analysis, ganglioneuromas are characterized by spindle-shaped cells with cell borders in a fibrillar matrix containing ganglion cells with large round nuclei, prominent nucleoli, and abundant eosinophilic cytoplasm.[3] Ganglioglioma must be differentiated from neuroblastoma, ganglioneuroblastoma, spinal schwannoma, spinal neurofibroma, adrenal adenoma, adrenal carcinoma, and pheochromocytoma.[4][5] Females are more commonly affected with ganglioneuroma than males.[5] Common complications of ganglioneuroma include paralysis, metastases, and local recurrence.[6] The prognosis of ganglioneuroma is excellent with treatment.[4] Symptoms of ganglioneuroma include dyspnea, chest pain, abdominal pain, bloating, pain and numbness in limbs, paresis, diarrhea, diaphoresis, and hirsuitism.[4] Common physical examination findings of ganglioneuroma include dyspnea, stridor, motor loss, sensory loss, diaphoresis, scoliosis, clitoromegaly, hirsuitism, and hypertension.[4] On chest x-ray, ganglioneuroma is characterized by a posterior mediastinal mass, which may cause rib spreading and foraminal erosion.[4] On CT scan, ganglioneuroma is characterized by a solid, well-circumscribed, and encapsulated mass that is iso to hypoattenuating to muscle.[4][5] On MRI scan, ganglioneuroma is characterized by a well circumscribed and encapsulatated mass with low signal intensity on T1-weighted images and intermediate to high signal intensity on T2-weighted images. Surgery is the mainstay of treatment for symptomatic ganglioneuroma. Adjunctive chemotherapy and radiotherapy may be required.[4]
Classification
According to International Neuroblastoma Pathology Classification (INPC), ganglioneuroma may be classified into two groups: Ganglioneuroma-maturing and ganglioneuroma-mature.[2]
Pathophysiology
Ganglioneuromas are derived from the primordial neural crest cells, which are undifferentiated cells of the sympathetic nervous system. Genes involved in the pathogenesis of ganglioneuroma include MYCN oncogene and chromosome 1p36. On gross pathology, ganglioneuromas are characterized by solid, white, firm, well-circumscribed, and nodular tumors. On microscopic histopathological analysis, ganglioneuromas are characterized by spindle-shaped cells with cell borders in a fibrillar matrix containing ganglion cells with large round nuclei, prominent nucleoli, and abundant eosinophilic cytoplasm.[3]
Causes
There are no established causes for ganglioneuroma.[4]
Differentiating brain tumors from other diseases
Ganglioglioma must be differentiated from neuroblastoma, ganglioneuroblastoma, spinal schwannoma, spinal neurofibroma, adrenal adenoma, adrenal carcinoma, and pheochromocytoma.[4][5]
Epidemiology and Demographics
The incidence of ganglioneuroma is approximately 1 per 100,000 children in the United States.[5] Ganglioneuroma is a rare disease that tends to affect children and young adults.[4] Females are more commonly affected with ganglioneuroma than males.[5] There is no racial predilection to ganglioneuroma.
Risk factors
There are no established risk factors for ganglioneuroma.[4]
Screening
Screening for ganglioneuroma is not recommended.[7]
Natural History, Complications and Prognosis
Common complications of ganglioneuroma include paralysis, metastases, and local recurrence.[8] The prognosis of ganglioneuroma is excellent with treatment.[4]
Staging
According to the International Neuroblastoma Staging System (INSS), there are six stages of ganglioneuroma based on clinical, radiologic, and surgical features.[5]
History and Symptoms
Symptoms of ganglioneuroma include dyspnea, chest pain, abdominal pain, bloating, pain and numbness in limbs, paresis, diarrhea, diaphoresis, and hirsuitism.[4]
Physical examination
Common physical examination findings of ganglioneuroma include dyspnea, stridor, motor loss, sensory loss, diaphoresis, scoliosis, clitoromegaly, hirsuitism, and hypertension.[4]
Laboratory Findings
Some patients with ganglioneuroma may have elevated concentrations of VMA (vanillylmandelic acid) or HVA (homovanillic acid) in urine.[4][5]
X Ray
On chest x-ray, ganglioneuroma is characterized by a posterior mediastinal mass, which may cause rib spreading and foraminal erosion. Plain x-rays may show a mass in the retroperitoneum, pelvis, or neck indicating the presence of metastasis.[4]
CT
Chest, abdomen, and pelvic CT scan may be helpful in the diagnosis of ganglioneuroma. Findings on CT scan suggestive of ganglioneuroma include a solid, well-circumscribed, and encapsulated mass that is iso to hypoattenuating to muscle.[4][5]
MRI
Chest and abdominal MRI scan may be helpful in the diagnosis of ganglioneuroma. On MRI scan, ganglioneuroma is characterized by a well circumscribed and encapsulatated mass with low signal intensity on T1-weighted images and intermediate to high signal intensity on T2-weighted images.[4]
Ultrasound
On ultrasound, ganglioneuroma is characterized by a homogeneous, hypoechoic, well circumscribed mass.[5]
Other Imaging Findings
Other imaging tests for ganglioneuroma include scintigraphy or medaiodobenzylguanidine (MIBG) scan.[5]
Other Diagnostic Studies
Other diagnostic studies for ganglioneuroma include biopsy, which demonstrates spindle-shaped cells with cell borders in a fibrillar matrix containing ganglion cells with large round nuclei, prominent nucleoli, and abundant eosinophilic cytoplasm.[4]
Medical Therapy
The predominant therapy for symptomatic ganglioneuroma is surgical resection. Adjunctive chemotherapy and radiotherapy may be required.[4]
Surgery
Surgery is the mainstay of treatment for symptomatic ganglioneuroma.[4]
References
- ↑ Introduction of ganglioneuroma. National Library of Medicine. https://www.nlm.nih.gov/medlineplus/ency/article/001437.htm
- ↑ 2.0 2.1 Okamatsu C, London WB, Naranjo A, Hogarty MD, Gastier-Foster JM, Look AT; et al. (2009). "Clinicopathological characteristics of ganglioneuroma and ganglioneuroblastoma: a report from the CCG and COG". Pediatr Blood Cancer. 53 (4): 563–9. doi:10.1002/pbc.22106. PMC 2730988. PMID 19530234.
- ↑ 3.0 3.1 Vasiliadis K, Papavasiliou C, Fachiridis D, Pervana S, Michaelides M, Kiranou M; et al. (2012). "Retroperitoneal extra-adrenal ganglioneuroma involving the infrahepatic inferior vena cava, celiac axis and superior mesenteric artery: A case report". Int J Surg Case Rep. 3 (11): 541–3. doi:10.1016/j.ijscr.2012.07.008. PMC 3437388. PMID 22907039.
- ↑ 4.00 4.01 4.02 4.03 4.04 4.05 4.06 4.07 4.08 4.09 4.10 4.11 4.12 4.13 4.14 4.15 4.16 4.17 4.18 4.19 4.20 D.Dx of ganglioneuroma. Dr Bruno Di Muzio and Dr Yuranga Weerakkody et al. Radiopaedia 2015. http://radiopaedia.org/articles/ganglioneuroma
- ↑ 5.00 5.01 5.02 5.03 5.04 5.05 5.06 5.07 5.08 5.09 5.10 Adam, O; Boia, ES (2007). "ganglioneuroma" (PDF). jurnalul pediatrului. 10 (39–40). Retrieved 10 September 2015.
- ↑ Complications of ganglioneuroma. National Library of Medicine. https://www.nlm.nih.gov/medlineplus/ency/article/001437.htm
- ↑ Fiori E, Pozzessere C, Lamazza A, Leone G, Borrini F, Schillaci A; et al. (2012). "Endoscopic treatment of ganglioneuroma of the colon associated with a lipoma: a case report". J Med Case Rep. 6: 304. doi:10.1186/1752-1947-6-304. PMC 3469395. PMID 22978818.
- ↑ Complications of ganglioneuroma. National Library of Medicine. https://www.nlm.nih.gov/medlineplus/ency/article/001437.htm