阴囊原发性滑膜肉瘤

IF 0.7 Q4 PATHOLOGY
Nourah Al-Oudah, Sara Alanazi, Sarah Saad Alotaibi, Nayef Alzahrani
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引用次数: 0

摘要

本报告概述了一例阴囊滑膜肉瘤病例。一名 36 岁的男性因阴囊肿胀就诊。病灶被完全切除,组织病理学检查显示为纺锤形细胞瘤。肿瘤的泛影角蛋白、AE1/AE3、上皮膜抗原(EMA)、TLE-1、CD99 和 BCL-2 染色阳性。细胞遗传学检测显示,位于 18q11.2 的 SS18 基因发生了染色体易位,与原发性滑膜肉瘤的诊断一致。一年后,患者出现肝、脊椎和肺转移,接受了全身化疗。治疗未能改善肝脏病灶,随后将其切除,而脊椎和肺部病灶则接受了放疗。患者目前仍健在,后续治疗仍在进行中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Primary Synovial Sarcoma of the Scrotum
The report outlines a case of synovial sarcoma in the scrotal region. A 36-year-old male presented with a scrotal swelling. The lesion was completely resected, whereas the histopathologic examination revealed a spindle cell tumor. The tumor stained positive for pancytokeratin, AE1/AE3, epithelial membrane antigen (EMA), TLE-1, CD99, and BCL-2. The cytogenetic testing showed a chromosomal translocation in the SS18 gene at 18q11.2, consistent with the diagnosis of primary synovial sarcoma. A year later, the patient developed liver, vertebrae, and lung metastasis, which was treated with systemic chemotherapy. Treatment failed to improve the hepatic lesion that was then resected, while the spine and lung lesions were followed by radiotherapy. The patient is now alive and subject to an outstanding follow-up.
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