Intravenous leiomyomatosis
(Redirected from IVLM)
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Template:Sonia Sandeep Js Sahar Memar Montazerin, M.D.[2]
Synonyms and keywords: Nesidioblastoma, IVLM
Overview
Intravenous leiomyomatosis is also refered as IVL. Intravenous leiomyomatosis is characterized by the extension into venous channels of histologically benign smooth muscle tumor arising from either the wall of a vessel or from a uterine leiomyoma. The etiology of intravenous leiomyomatosis is unclear. Intravenous leiomyomatosis must be differentiated from other diseases such as renal malignancies and sarcomas. The median age is 45 years, with patients age ranging from 26 to 70 years old. Only females may develop intravenous leiomyomatosis. Findings on CT scan diagnostic of intravenous leiomyomatosis include an irregular mass exhibiting heterogeneous enhancement with extension into adjacent veins. Findings on an ultrasound imaging diagnostic of intravenous Leiomyomatosis include a vascularized thrombi within the pelvic veins and Inferior vena cava. Findings on MRI diagnostic of intravenous leiomyomatosis include a leiomyomatous lesion or a distorted uterus with projections into vasculature. Surgery is the mainstay of therapy for intravenous leiomyomatosis. It can grow into lymphatics /veins.
Historical Perspective
- Intravenous leiomyomatosis first described in 1896 by German Pathologist Birch-Hirschfeld.[1]
- First case of leiomyo-matosis of pelvic origin with intravascular extension to cardiac cavities was described in 1907 in Germany by Dürck and Hörmann.[2]
Classification
- There is no established system for the classification of intravenous leiomyomatosis.
Pathophysiology
- Intravenous leiomyomatosis is characterized by the extension into venous channels of histologically benign smooth muscle tumors arising from either the wall of a vessel or from a uterine leiomyoma.[3]
- Approximately 40% of leiomyomata have cytogenetic abnormalities.
- They are benign tumors of uterus that extend to venous system but do not invade the surrounding tissues. [4]
- They contains receptors responsive to estrogen and progesterone and hence response to these hormones. [5]
- It is also referred as quasi-malignant behavior due to its speedy spreading behavior.[6]
- On microscopy it is seen as benign, well-differentiated tumor with smooth muscle cell growing within veins as worm-like projections.
- Tumor cells shows bizarre nuclear morphology with hyperchromatic multilobated nuclei.
- The mitotic activity is low, with mitotic index of less than 1 per 50 high-power fields.
Causes
- The etiology of intravenous leiomyomatosis is unclear.[7]
Differentiating Intravenous Leiomyomatosis from other Diseases
- Intravenous leiomyomatosis must be differentiated from other conditions such as intravenous thrombus, leiomyosarcoma, right atrial myxoma and thrombosis of carcinomas, for example, renal cell carcinoma, hepatocellular carcinoma, and adrenocortical carcinoma.[8][7]
- For more information on intravenous leiomyomatosis differential diagnosis, please click here.
Epidemiology and Demographics
- There is no available data on the exact incidence of intravenous leiomyomatosis.
- The median age at the time of diagnosis of IVL is 45 years, with patients age ranging from 26 to 70 years old. [9]
- Female are exclusively affected with intravenous leiomyomatosis.[10]
- Intravenous leiomyomatosis is seen more commonly in white females.[11]
Risk Factors
- Common risk factors in the development of intravenous leiomyomatosis are age, cytogenetic abnormalities , and prior history of uterine leiomyoma, and/or hysterectomy.[12]
Screening
- There is insufficient evidence to recommend routine screening for intravenous leiomyomatosis.
Natural History, Complications and Prognosis
- If left untreated, patients with intravenous leiomyomatosis may progress to develop congestive heart failure, venous obstruction, and sudden death.[13][7][14]
- Other possible complications of intravenous leiomyomatosis include tumor recurrence, and metastasis.[15][16]
- Prognosis is generally good.
Diagnosis
Diagnostic Criteria
- There is no specific diagnostic Criteria for intravenous leiomyomatosis.
- Diagnosis may be challenging. However, a history of A history of hysterectomy or the presence of uterine leiomyomas may be helpful.[7]
History and Symptoms
- Patients may be asymptomatic or have symptoms related to uterine leiomyomas.[17][18][19]
- Symptoms related to uterine leiomyoma may include abdominal pain, abnormal uterine bleeding, and abdominal distension.[20]
- Symptoms of intravenous Leiomyomatosis due to extension to great veins or invoving the heart may include dyspnoea, loss of consciousness, lower extremity edema, chest pain, abdominal pain, and fatigue.
Physical Examination
- Patients with intravenous Leiomyomatosis usually depends on location and extension of the tumor which may include jugular venous distention, increased pulse rate, shifting dullness in abdominal exam suggestive of ascites, and lower extremity edema.[21]
Laboratory Findings
- There are no specific laboratory findings associated with intravenous Leiomyomatosis.
Electrocardiogram
- There are no ECG findings associated with intravenous Leiomyomatosis.
X-ray
- There are no x-ray findings associated with intravenous Leiomyomatosis.
Echocardiography or Ultrasound
- Echocardiography/ultrasound may be helpful in the diagnosis of intravenous Leiomyomatosis.
- Findings on an ultrasound imaging diagnostic of intravenous Leiomyomatosis include a vascularized thrombi within the pelvic veins and IVC.[7]
- Echocardiography may show findings consistent with right atrial involvement of the tumor.
- Possible findings of IVL on echocardiography include hyperechoic elongated mobile mass extending from the inferior vena cava and an irregular lesion in the right atrium and sometimes with protrusion into the right ventricle.[22]
CT scan
- Pelvic CT scan may be helpful in the diagnosis of intravenous leiomyomatosis.[23]
- Findings on CT scan diagnostic of intravenous leiomyomatosis include an irregular mass exhibiting heterogeneous enhancement with extension into adjacent veins.
MRI
- Pelvic MRI may be helpful in the diagnosis of intravenous leiomyomatosis.[7]
- Findings on MRI diagnostic of intravenous leiomyomatosis include a leiomyomatous lesion or a distorted uterus with projections into vasculature.
- The tumor usually shows low signal intensity similar to that of smooth muscle on T2-weighted images and low to intermediate signal intensity on T1-weighted images.
- The appearance of the lesion varies according to its smooth muscle cell and fibrous tissue content.
Other Imaging Findings
- There are no other imaging findings associated with intravenous leiomyomatosis.
Other Diagnostic Studies
- There are no other diagnostic studies associated with intravenous leiomyomatosis.
Treatment
Medical Therapy
- There is no treatment for intravenous leiomyomatosis.
Surgery
- Surgery is the treatment of choice, and complete removal of the tumor is mandatory.
- Recurrences may occur up to 15 years after the primary occurrence in patients with Incomplete resection of the tumor.[24]
- Bilateral oophorectomy causes shutdown of hormonal stimulation hence helps preventing recurrence.[25]
- Surgical removal can be done in single or staged procedures.[26]
Primary Prevention
- There are no primary preventive measures available for IVL.
Secondary Prevention
- There are no secondary preventive measures available for IVL.
References
- ↑ Quade BJ, Dal Cin P, Neskey DM, Weremowicz S, Morton CC (2002). "Intravenous leiomyomatosis: molecular and cytogenetic analysis of a case". Mod Pathol. 15 (3): 351–6. doi:10.1038/modpathol.3880529. PMID 11904348.
- ↑ Stolf NA, dos Santos GG, Haddad VL (1999). "Unusual abdominal tumors with intracardiac extension. Two cases with successful surgical resection". Rev Hosp Clin Fac Med Sao Paulo. 54 (5): 159–64. PMID 10788838.
- ↑ Mariyappa N, Manikyam UK, Krishnamurthy D, Preeti K, Agarwal Y, Prakar U (2012). "Intravenous leiomyomatosis". Niger J Surg. 18 (2): 105–6. doi:10.4103/1117-6806.103122. PMC 3762011. PMID 24027407.
- ↑ Dal Cin P, Quade BJ, Neskey DM, Kleinman MS, Weremowicz S, Morton CC (2003). "Intravenous leiomyomatosis is characterized by a der(14)t(12;14)(q15;q24)". Genes Chromosomes Cancer. 36 (2): 205–6. doi:10.1002/gcc.10159. PMID 12508249.
- ↑ Dal Cin P, Quade BJ, Neskey DM, Kleinman MS, Weremowicz S, Morton CC (2003). "Intravenous leiomyomatosis is characterized by a der(14)t(12;14)(q15;q24)". Genes Chromosomes Cancer. 36 (2): 205–6. doi:10.1002/gcc.10159. PMID 12508249.
- ↑ Quade BJ, Dal Cin P, Neskey DM, Weremowicz S, Morton CC (2002). "Intravenous leiomyomatosis: molecular and cytogenetic analysis of a case". Mod Pathol. 15 (3): 351–6. doi:10.1038/modpathol.3880529. PMID 11904348.
- ↑ 7.0 7.1 7.2 7.3 7.4 7.5 Fasih, Najla; Prasad Shanbhogue, Alampady K.; Macdonald, David B.; Fraser-Hill, Margaret A.; Papadatos, Demetrios; Kielar, Ania Z.; Doherty, Geoffrey P.; Walsh, Cynthia; McInnes, Matthew; Atri, Mostafa (2008). "Leiomyomas beyond the Uterus: Unusual Locations, Rare Manifestations". RadioGraphics. 28 (7): 1931–1948. doi:10.1148/rg.287085095. ISSN 0271-5333.
- ↑ Lee, Sak; Kim, Do-Kyun; Narm, Kyoung Shik; Cho, Sang-Ho (2011). "Pulmonary Artery Embolization of Intravenous Leiomyomatosis Extending into the Right Atrium". The Korean Journal of Thoracic and Cardiovascular Surgery. 44 (3): 243–246. doi:10.5090/kjtcs.2011.44.3.243. ISSN 2233-601X.
- ↑ Canzonieri V, D'Amore ES, Bartoloni G, Piazza M, Blandamura S, Carbone A (1994). "Leiomyomatosis with vascular invasion. A unified pathogenesis regarding leiomyoma with vascular microinvasion, benign metastasizing leiomyoma and intravenous leiomyomatosis". Virchows Arch. 425 (5): 541–5. PMID 7850080.
- ↑ Poliquin V, Victory R, Vilos GA (2008). "Epidemiology, presentation, and management of retroperitoneal leiomyomata: systematic literature review and case report". J Minim Invasive Gynecol. 15 (2): 152–60. doi:10.1016/j.jmig.2007.12.009. PMID 18312983.
- ↑ Poliquin V, Victory R, Vilos GA (2008). "Epidemiology, presentation, and management of retroperitoneal leiomyomata: systematic literature review and case report". J Minim Invasive Gynecol. 15 (2): 152–60. doi:10.1016/j.jmig.2007.12.009. PMID 18312983.
- ↑ Leitman, M.; Kuperstein, R.; Medalion, B.; Stamler, A.; Porat, E.; Rosenblatt, S.; Konen, E.; Krakover, R.; Vered, Z. (2008). "A highly unusual right atrial mass presented in two women". European Heart Journal - Cardiovascular Imaging. 9 (6): 833–834. doi:10.1093/ejechocard/jen173. ISSN 2047-2412.
- ↑ Schäfer HM, Isaak A, Gürke L (2017). "Case report of an intracaval leiomyomatosis 10 months after complete hysterectomy". Int J Surg Case Rep. 35: 1–3. doi:10.1016/j.ijscr.2017.03.031. PMC 5394212. PMID 28414995.
- ↑ Kocica, Mladen J.; Vranes, Mile R.; Kostic, Dusan; Kostic, Natasa Kovacevic-; Lackovic, Vesna; Mihajlovic, Vesna Bozic-; Velinovic, Milos M.; Mikic, Aleksandar Dj.; Kalezic, Nevena Dimitrijevic- (2005). "Intravenous leiomyomatosis with extension to the heart: Rare or underestimated?". The Journal of Thoracic and Cardiovascular Surgery. 130 (6): 1724–1726. doi:10.1016/j.jtcvs.2005.08.021. ISSN 0022-5223.
- ↑ Evans AT, Symmonds RE, Gaffey TA (February 1981). "Recurrent pelvic intravenous leiomyomatosis". Obstet Gynecol. 57 (2): 260–4. PMID 7465135.
- ↑ Awonuga, Awoniyi O.; Rotas, Michael; Imudia, Anthony N.; Choi, Christine; Khulpateea, Neekianund (2008). "Recurrent benign metastasizing leiomyoma after hysterectomy and bilateral salpingo-oophorectomy". Archives of Gynecology and Obstetrics. 278 (4): 373–376. doi:10.1007/s00404-008-0581-z. ISSN 0932-0067.
- ↑ Nakayama Y, Kitamura S, Kawachi K, Kawata T, Fukutomi M, Hasegawa J; et al. (1994). "Intravenous leiomyomatosis extending into the right atrium". Cardiovasc Surg. 2 (5): 642–5. PMID 7820530.
- ↑ Moorjani N, Kuo J, Ashley S, Hughes G (2005). "Intravenous uterine leiomyosarcomatosis with intracardial extension". J Card Surg. 20 (4): 382–5. doi:10.1111/j.1540-8191.2005.200476.x. PMID 15985146.
- ↑ Poliquin V, Victory R, Vilos GA (2008). "Epidemiology, presentation, and management of retroperitoneal leiomyomata: systematic literature review and case report". J Minim Invasive Gynecol. 15 (2): 152–60. doi:10.1016/j.jmig.2007.12.009. PMID 18312983.
- ↑ Vaquero ME, Magrina JF, Leslie KO (2009). "Uterine smooth-muscle tumors with unusual growth patterns". J Minim Invasive Gynecol. 16 (3): 263–8. doi:10.1016/j.jmig.2009.01.013. PMID 19423058.
- ↑ Andrade LA, Torresan RZ, Sales JF, Vicentini R, De Souza GA (1998). "Intravenous leiomyomatosis of the uterus. A report of three cases". Pathol. Oncol. Res. 4 (1): 44–7. PMID 9555121.
- ↑ Kang LQ, Zhang B, Liu BG, Liu FH (January 2012). "Diagnosis of intravenous leiomyomatosis extending to heart with emphasis on magnetic resonance imaging". Chin. Med. J. 125 (1): 33–7. PMID 22340462.
- ↑ Xu, Zhi-Feng (2013). "Uterine intravenous leiomyomatosis with cardiac extension: Imaging characteristics and literature review". World Journal of Clinical Oncology. 4 (1): 25. doi:10.5306/wjco.v4.i1.25. ISSN 2218-4333.
- ↑ Yanagiya A, Yamada O, Nanbu T, Hamada H, Takada J, Matsuura M; et al. (2015). "[One-stage resection of intravenous leiomyomatosis extending into the right atrium]". Kyobu Geka. 68 (3): 188–91. PMID 25743551.
- ↑ Castelli P, Caronno R, Piffaretti G, Tozzi M (2006). "Intravenous uterine leiomyomatosis with right heart extension: successful two-stage surgical removal". Ann Vasc Surg. 20 (3): 405–7. doi:10.1007/s10016-006-9024-0. PMID 16583249.
- ↑ Nam MS, Jeon MJ, Kim YT, Kim JW, Park KH, Hong YS (2003). "Pelvic leiomyomatosis with intracaval and intracardiac extension: a case report and review of the literature". Gynecol Oncol. 89 (1): 175–80. PMID 12694674.