Journals / Şişli Etfal Hastanesi Tıp Bülteni / 2016 / Cilt: 50 - Sayı: 4

Round ligaman kaynaklı retroperitoneal inflamatuar myofibroblastik tümör

Retroperitoneal Inflammatory Myofibroblastic Tumor Originating from Round Ligament

Pages
330–333
DOI
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Uterine round ligament is a very rare location for IMT.Case: We report the morphological, immunohistochemical and clinical features of an IMT which is located in the retroperitoneum / uterine round ligament of a young woman in this paper.Conclusion: It is essential to differentiate IMT from benign and malignant mimickers for providing an appropriate therapy and follow-up.

📌 3 Key Takeaways

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Objective & Hypothesis:Objective: Inflammatory myofibroblastic tumor (IMT) is a rare tumor.
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Key Findings & Data:The etiology and biological behaviour is controversial.
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Conclusion & Impact:Uterine round ligament is a very rare location for IMT.Case: We report the morphological, immunohistochemical and clinical features of an IMT which is located in the retroperitoneum / uterine round ligament of a young woman in this paper.Conclusion: It is essential to differentiate IMT from benign and malignant mimickers for providing an appropriate therapy and follow-up.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Objective: Inflammatory myofibroblastic tumor (IMT) is a rare tumor. The etiology and biological behaviour is controversial. It could be seen in many different anatomical sites, however it is commonly seen in the lungs, mesentery, genitourinary tract and retroperitoneum. Uterine round ligament is a very rare location for IMT.Case: We report the morphological, immunohistochemical and clinical features of an IMT which is located in the retroperitoneum / uterine round ligament of a young woman in this paper.Conclusion: It is essential to differentiate IMT from benign and malignant mimickers for providing an appropriate therapy and follow-up.

Özet

Amaç: İnflamatuar myofibroblastik tümör (İMT), nadir görülen bir tümördür. Etyolojisi ve biyolojik davranışı tartışmalıdır. Genellikle akciğerde, mezenterde, genitouriner traktta, retroperitonda bildirilmesine rağmen birçok farklı lokalizasyonda bulunabilir. Uterin round ligaman oldukça nadir bir lokalizasyondur. Olgu: Genç bir hastada, retroperitonda / uterin round ligamanda yerleşmiş bir inflamatuar myofibroblastik tümör vakasını, morfolojik, immunhistokimyasal ve klinik özellikleriyle birlikte değerlendirdik.Sonuç: Uygun tedavi ve takip için İMT'yi malign ve benign taklitçilerinden ayırmak önemlidir.

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Cite This Article

KOÇ, N., CESUR, S., İHVAN, A. N., BAŞ, Y., POLAT, M. (2016). Round ligaman kaynaklı retroperitoneal inflamatuar myofibroblastik tümör. Şişli Etfal Hastanesi Tıp Bülteni, Cilt: 50 - Sayı: 4, 330–333. https://ajindex.com/articles/364142

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References (3)

  1. Pungpapong S, Geiger XJ, Raimondo M. Inflammatory myofibroblastic tumor presenting as a pancreatic mass: a case report and review of the literature. JOP 2004; 5: 360-7.
  2. Rabban JT, Zaloudek CJ, Shekitka KM, Tavassoli FA.Inflammatory myofibroblastic tumor of the uterus: a clinicopathologic study of 6 cases emphasizing distinction from aggressive mesenchymal tumors. Am J Surg Pathol 2005; 29: 1348-55. [CrossRef] Coffin CM, Watterson J, Priest JR, Dehner LP. Extrapulmonary inflammatory myofibroblastic tumor (inflammatory pseudotumor) a clinicopathologic and immunohistochemical study of 84 cases. Am J Surg Pathol 1995; 19: 859-72. [CrossRef] Gleason BC, Hornick JL. Inflammatory myofibroblastic tumours: where are we now? J Clin Pathol. 2008; 61: 428-37. [CrossRef] Takeda S, Onishi Y, Kawamura T, Maeda H. Clinical spectrum of pulmonary inflammatory myofibroblastic tumor. Interact Cardiovasc Thorac Surg 2008; 7: 629-33. [CrossRef] Dutta V, Manoj MG, Malik A, Kumar P. ALK negative inflammatory myofibroblastic tumor of the orbit: a masquerading entity. Indian J Ophthalmol 2014; 62: 627. [CrossRef] Park S, Ro JY, Lee DH, Choi SY, Koo H. Immunoglobulin G4-associated inflammatory pseudotumor of urinary bladder: a case report. Ann Diagn Pathol 2013; 17: 540-3. [CrossRef] Parra-Herran C, Quick CM, Howitt BE, Dal Cin P, Quade BJ, Nucci MR. Inflammatory myofibroblastic tumor of the uterus: clinical and pathologic review of 10 cases including a subset with aggressive clinical course. Am J Surg Pathol 2015; 39: 157- 68. [CrossRef] Gilani SM, Kowalski PJ. Inflammatory myofibroblastic tumour: a rare entity with wide differential diagnosis. Pathologica 2014; 106: 1-6.
  3. Yantiss RK, Spiro IJ, Compton CC, Rosenberg AE. Gastrointestinal stromal tumor versus intra-abdominal fibromatosis of the bowel wall: a clinically important differential diagnosis. Am J Surg Pathol 2000; 24: 947-57. [CrossRef] Miettinen M, Wang ZF, Lasota J. DOG1 antibody in the differential diagnosis of gastrointestinal stromal tumors: a study of 1840 cases. Am J Surg Pathol 2009; 33: 401-8. [CrossRef] Le Guellec S, Soubeyran I, Rochaix P, Filleron T, Neuville A, Hostein I, et al. CTNNB1 mutation analysis is a useful tool for the diagnosis of desmoid tumors: a study of 260 desmoid tumors and 191 potential morphologic mimics. Mod Pathol 2012; 25: 1551-8. [CrossRef]