Solitary Fibrous Tumor of the Prostate: Case Report and Review of the Literature

M. E. Ouazzani, A. Nebgui, H. Rachidi, K. Rabbani, A. Louzi, H. Rais, A. Belbachir
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Abstract

Solitary fibrous tumor (SFT), typically found in the pleura, is exceptionally rare in the prostate. We present the case of a 54-year-old man with prostatic SFT, initially revealed as an abdominopelvic mass. Subsequent investigations shown a vascular tumor. The pathological examination found a 23-cm tumor originating from the prostate, composed of short spindle-shaped and polygonal cells with mild nuclear atypia. Occasional mitoses were observed, with vascular invasion. Immunohistochemically, the tumor cells strongly expressed CD34 and STAT6. The maximum Ki-67 labeling index for the tumor cells was 4%. This case report has highlighted one of the rare occurrences of solitary fibrous tumor. A comprehensive microscopic examination paired with an immunohistochemical analysis will be necessary to establish an accurate diagnosis.
前列腺单发纤维性肿瘤:病例报告和文献综述
孤立性纤维瘤(SFT)通常出现在胸膜,但在前列腺中却异常罕见。我们介绍了一例 54 岁男性前列腺 SFT 患者的病例,患者最初表现为腹盆腔肿块。随后的检查显示为血管瘤。病理检查发现,肿瘤长 23 厘米,源自前列腺,由短纺锤形和多角形细胞组成,核轻度不典型。偶见有丝分裂,并伴有血管侵犯。免疫组化结果显示,肿瘤细胞强烈表达 CD34 和 STAT6。肿瘤细胞的最大 Ki-67 标记指数为 4%。本病例报告强调了一种罕见的单发纤维瘤。要做出准确诊断,必须进行全面的显微镜检查和免疫组化分析。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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