Journals / Cerrahpaşa Medical Journal / 2022 / Cilt: 46 - Sayı: 1

A Rare Case of an Uterine Intravenous Leiomyomatosis

Pages
83–85
Publication Date
2022-10-12
DOI
—
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AI Summary & Key Takeaways

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

Subsequent histopathological and immunohistochemical examination confirmed the diagnosis as intravenous leiomyomatosis.

📌 3 Key Takeaways

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Objective & Hypothesis:Intravenous leiomyomatosis is a rare benign neoplasm originating from smooth muscle cells.
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Key Findings & Data:Although histopathologically benign, its behavior may be aggressive and fatal outcomes can occur.
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Conclusion & Impact:Subsequent histopathological and immunohistochemical examination confirmed the diagnosis as intravenous leiomyomatosis.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Intravenous leiomyomatosis is a rare benign neoplasm originating from smooth muscle cells. Although histopathologically benign, its behavior may be aggressive and fatal outcomes can occur. However, it is very difficult to diagnose this entity, and intravenous leiomyomatosis is usually only suspected intraoperatively or after pathological analysis. In this article, we presented an interesting case of intravenous leiomyomatosis who was diagnosed intraoperatively and complicated with massive bleeding. Subsequent histopathological and immunohistochemical examination confirmed the diagnosis as intravenous leiomyomatosis.

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Cite This Article

MÜFTÜOĞLU, K. H., KINAY, T., KORKMAZ, V., MESCİ, Ç. G., ÜNSAL, M., ŞAHİN, E. K., YÜKSEL, D. (2022). A Rare Case of an Uterine Intravenous Leiomyomatosis. Cerrahpaşa Medical Journal, Cilt: 46 - Sayı: 1, 83–85. https://ajindex.com/articles/473104

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