原发性肺低分化纤维肉瘤:罕见病例与诊断难题。

IF 0.9 Q4 ONCOLOGY
Rare Tumors Pub Date : 2024-02-29 eCollection Date: 2024-01-01 DOI:10.1177/20363613241234201
Aida Ayadi, Yoldez Houcine, Chirine Moussa, Houda Rouis, Tarek Abid, Begueret Hugues, François Le Loarer
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引用次数: 0

摘要

低度纤维肉瘤(LGFMS)是一种罕见的低度恶性软组织肿瘤,常被误诊为良性肿瘤或更罕见的恶性肿瘤类型。这种肿瘤常见于青壮年,通常发生在四肢近端深部或躯干,经常复发,多年后可转移至肺部。内脏型 LGFMS 极其罕见。只有少数肺部原发性 LGFMS 病例被报道过。在此,我们将介绍发生在肺部的埃文斯肿瘤的临床、大体、显微和免疫组化特征,并回顾相关文献,讨论这一特殊定位的鉴别诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Primary lung low-grade fibromyxoid sarcoma: A rare case with A diagnostic dilemma.

Low-grade fibromyxoid sarcoma (LGFMS) is a rare, low-grade malignant soft tissue tumor that is often mistaken for benign or more rarely malignant tumor types. Commonly, this tumor affects young adults and typically arises in the deep proximal extremities or trunk with frequent recurrences and can metastasize to the lungs many years late. Visceral LGFMS is extremely rare. Only a few cases of primary LGFMS of the lung have been reported. Here, we present the clinical, gross, microscopic, and immunohistochemical characteristics of Evans tumor occurring in the lung with a review of the literature and discuss the differential diagnosis in this exceptional localization.

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Rare Tumors
Rare Tumors ONCOLOGY-
CiteScore
1.50
自引率
0.00%
发文量
15
审稿时长
15 weeks
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