Journals / Türk Göğüs Kalp Damar Cerrahisi Dergisi / 2010 / Cilt: 18 - Sayı: 1

Mediasten yerleşimli hemanjiyoperisitoma: Olgu sunumu

Hemangiopericytoma located in the mediastinum: A case report

Pages
74–77
Publication Date
2022-09-02
DOI
—
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AI Summary & Key Takeaways

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

Details of clinic, pathologic and radiographic features are presented.

📌 3 Key Takeaways

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Objective & Hypothesis:emangiopericytomas, which arise from cells (pericytes) that are wrapped around the pericapillary arterioles, are commonly located in the soft tissue of the thigh and retroperitoneum.
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Key Findings & Data:Fewer than 20 cases were reported and while one fourth of them was benign and the remainder was malignant.
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Conclusion & Impact:Details of clinic, pathologic and radiographic features are presented.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

emangiopericytomas, which arise from cells (pericytes) that are wrapped around the pericapillary arterioles, are commonly located in the soft tissue of the thigh and retroperitoneum. Hemangiopericytoma in the mediastinum is extremely rare. Fewer than 20 cases were reported and while one fourth of them was benign and the remainder was malignant. The malignant potential of hemangiopericytoma is a distinctive characteristic when compared to the other vascular tumors. A high-signal area on T2-weighted magnetic resonance imaging and a massive bleeding mass during the operation are the characteristic features of hemangiopericytoma. Complete resection is the only effective treatment option for this vascular slow-growing tumor. In this article, we report a case of a 23-year-old male who was treated by complete surgical resection of the tumor. Details of clinic, pathologic and radiographic features are presented.

Özet

Hemanjiyoperisitomalar perikapiller arteriollerin etrafını saran hücrelerden (perikist) köken alan, genellikle retroperiton ve uyluğa ait yumuşak dokuda yerleşen tümörlerdir. Mediastinal yerleşimli hemanjiyoperisitoma oldukça enderdir. Bildirilmiş 20’den az olgu bulunmaktadır ve bunların dörtte biri benign iken diğerleri maligndir. Hemanjiyoperisitomanın malign olma potansiyeli diğer vasküler tümörler ile karşılaştırıldığında ayırt edici bir özelliktir. T2 ağırlıklı manyetik rezonans görüntülemede yüksek sinyalli bir alan ve ameliyat sırasında masif kanamalı bir kitle hemanjiyoperisitomanın karakteristik özelliklerindendir. Bu yavaş büyüyen vasküler tümörün tek etkili tedavi seçeneği tam rezeksiyondur. Bu yazıda tam cerrahi rezeksiyon uygulanarak tedavi edilen 23 yaşında erkek bir olgu klinik, patolojik ve radyografik özellikleri ile sunuldu.

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Cite This Article

GÜNHAN, Ö., GENÇ, O., YÜCEL, O., KAVAKLI, K. (2022). Mediasten yerleşimli hemanjiyoperisitoma: Olgu sunumu. Türk Göğüs Kalp Damar Cerrahisi Dergisi, Cilt: 18 - Sayı: 1, 74–77. https://ajindex.com/articles/424917

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