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前列腺原发性促纤维组织增生性小圆细胞瘤

Primary desmoplastic small round cell tumour of the prostate.

作者信息

Qian Jingyu, Yang Yanjin, Xie Xin, Kang Yifan, Zhong Jinjing, Chen Xueqin, Chen Ni, Zhou Qiao, Nie Ling

机构信息

Department of Pathology, West China Hospital, West China Medical School, Sichuan University, Chengdu, Sichuan, China.

Laboratory of Pathology, West China Hospital, Sichuan University, Chengdu, Sichuan, China.

出版信息

J Clin Pathol. 2024 Dec 18;78(1):64-69. doi: 10.1136/jcp-2024-209660.

Abstract

Desmoplastic small round cell tumour (DSRCT) is a highly aggressive soft-tissue sarcoma with distinctive morphological features and characteristic gene fusion. DSRCT occurs in a variety of anatomic sites, with abdominal cavity being the most common location. Primary DSRCTs arising in the male genital system are exceedingly rare, with no documented definitive cases of primary DSRCT of the prostate to date, although 28 cases of DSRCT in the testicular or paratesticular regions have been reported. We here present two cases of primary DSRCT of the prostate. Both cases demonstrated the distinct morphology and the typical multiphenotypic immunohistochemical profile, and the characteristic fusion verified by fluorescent in situ hybridisation. Our cases expand the anatomic distribution of primary DSRCT and highlight the importance of considering this rare tumour in the differential diagnoses of small cell malignancies of the prostate.

摘要

促纤维组织增生性小圆细胞肿瘤(DSRCT)是一种具有独特形态学特征和特征性基因融合的高度侵袭性软组织肉瘤。DSRCT发生于多种解剖部位,腹腔是最常见的部位。起源于男性生殖系统的原发性DSRCT极为罕见,迄今为止尚无前列腺原发性DSRCT的确切病例记录,尽管已有28例睾丸或睾丸旁区域的DSRCT病例报道。我们在此报告2例前列腺原发性DSRCT。两例均表现出独特的形态学及典型的多表型免疫组化特征,并通过荧光原位杂交验证了特征性融合。我们的病例扩展了原发性DSRCT的解剖分布范围,并强调了在前列腺小细胞恶性肿瘤的鉴别诊断中考虑这种罕见肿瘤的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cde9/11671908/67e2ccbec73d/jcp-78-1-g001.jpg

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