荧光原位杂交显示SS18免疫化学表达和重排伴骨化和钙化的滑膜肉瘤

Q4 Medicine
Luis A. Acosta-Calderón , César Lara-Torres , Leonardo S. Lino-Silva , Claudia H. Caro-Sánchez , Mayra E. Jiménez-De Los Santos , Hugo R. Domínguez-Malagón
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引用次数: 0

摘要

滑膜肉瘤是一种起源不明的软组织肿瘤。一般来说,它是一种单相梭形细胞肿瘤,可以具有腺样结构。骨化和钙化是一种罕见的现象,只有少数病例报告。我们报告一例年轻男性右脚滑膜肉瘤。组织学检查显示肿瘤性骨样沉积和粗钙化。通过免疫组织化学检测SS18的表达和通过荧光原位杂交检测SS18基因的重排来证实诊断。我们回顾了滑膜肉瘤伴明显骨化或钙化的文献,据我们所知,这是第一例通过免疫组织化学表达SS18的病例。主要的鉴别诊断是骨肉瘤(原发性骨和骨外)和硬化性上皮样纤维肉瘤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synovial sarcoma with ossification and calcification with SS18 immunochemical expression and rearrangement by fluorescent in situ hybridization

Synovial sarcoma is a soft tissue tumor of uncertain origin. Generally, it is a monophasic spindle cell neoplasm that can have glandular-like structures. Ossification and presence of calcification is a rare phenomenon with only a few reported cases. We present the case of a young male with a synovial sarcoma of the right foot. Histology revealed prominent deposits of tumoral osteoid and coarse calcifications. The diagnosis was confirmed by the expression of SS18 by immunohistochemistry and the demonstration of the rearrangement of the SS18 gene by fluorescent in situ hybridization. We reviewed the literature for synovial sarcoma with prominent ossification or calcification, and to the best of our knowledge, this is the first case with expression of SS18 by immunohistochemistry. The main differential diagnoses are osteosarcoma (both primary of bone and extraosseous) and sclerosing epithelioid fibrosarcoma.

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来源期刊
Revista Espanola de Patologia
Revista Espanola de Patologia Medicine-Pathology and Forensic Medicine
CiteScore
0.90
自引率
0.00%
发文量
53
审稿时长
34 days
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