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[Epithelioid sarcoma of the right hand].

机译:[右上皮样肉瘤]。

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摘要

A 35-year-old man presented with swelling, indurations and nodules on the thumb, wrist and fingers of the right hand. History revealed that the findings were slowly progressive and had been present for at least eight years. Histopathologic analysis of a nodule showed a diffuse infiltrate with atypical spindle-shaped cells and expression of cytokeratin, epithelial membrane antigen (EMA) and CD34; the diagnosis of epithelioid sarcoma (ES) was made. Because of diffuse extension of the tumor, forearm amputation was performed along with axillary dissection and local radiotherapy because of axillary lymph node metastases. ES is a rare subtype of soft tissue sarcoma with a harmless appearance and indolent course over years. ES represents a diagnostic challenge, with consequent delay in diagnosis and adequate treatment. The most important measure in the treatment of ES is early surgical excision with adjuvant radiotherapy if local metastases are present.
机译:一名35岁的男子在右手的拇指,手腕和手指上出现肿胀,硬结和结节。历史表明,这些发现是缓慢进行的,已经存在了至少八年。结节的组织病理学分析显示非典型梭形细胞弥漫性浸润,并表达细胞角蛋白,上皮膜抗原(EMA)和CD34。诊断为上皮样肉瘤(ES)。由于肿瘤弥漫性扩散,由于腋窝淋巴结转移,因此进行了前臂截肢,腋窝淋巴结清扫和局部放疗。 ES是一种罕见的软组织肉瘤亚型,多年来无害且无病。 ES代表了诊断挑战,因此延迟了诊断和适当的治疗。如果存在局部转移,ES治疗中最重要的措施是早期手术切除并辅以放疗。

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