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阴囊细胞性血管纤维瘤:一例报告并文献复习

Scrotal cellular angiofibroma: A case report and review of the literature.

作者信息

Buchinsky David, Pahouja Gaurav

机构信息

Wright State University Boonshoft School of Medicine, Division of Urology, Dayton, OH, USA.

出版信息

Urol Case Rep. 2024 Sep 25;57:102850. doi: 10.1016/j.eucr.2024.102850. eCollection 2024 Nov.

Abstract

Scrotal cellular angiofibroma (CAF) is a rare, benign, soft-tissue paratesticular tumor that has been sporadically reported previously. We present a case of a 55-year old male with a scrotal mass ultimately diagnosed with scrotal CAF. Immunohistochemical analysis stained positively for desmin, CD34, and estrogen receptor. Our series is one of the only published to date demonstrating desmin-positive paratesticular CAF. Diagnosis of CAF remains difficult due to the sparsity of paratesticular CAF, its similar characteristics to spindle cell lipoma (SCL), and variability in immunohistochemical reporting.

摘要

阴囊细胞性血管纤维瘤(CAF)是一种罕见的良性睾丸旁软组织肿瘤,此前曾有过零星报道。我们报告一例55岁男性阴囊肿物,最终诊断为阴囊CAF。免疫组化分析显示结蛋白、CD34和雌激素受体呈阳性。我们的病例系列是迄今为止仅有的已发表的显示结蛋白阳性的睾丸旁CAF病例之一。由于睾丸旁CAF病例稀少、其特征与梭形细胞脂肪瘤(SCL)相似以及免疫组化报告存在差异,CAF的诊断仍然困难。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cda4/11474220/9a41b42e6f58/gr1.jpg

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