组织细胞肉瘤:罕见的遭遇

N. Kartha, K. Sobhanakumari, Predesh Jose
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引用次数: 0

摘要

组织细胞肉瘤是一种罕见的起源于组织细胞克隆的血淋巴肿瘤。病变可发生在淋巴结或结外部位。少数病例表现为独特的皮肤病变。最终诊断由免疫组织化学作出。治疗方法取决于疾病的严重程度。在此,我们报告一例65岁女性的组织细胞肉瘤,表现为前臂和大腿皮下肿胀和溃疡合并结节,并转移到肺部,并接受全身化疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Histiocytic sarcoma: An encounter with a rarity
Histiocytic sarcoma is a rare hematolymphoid neoplasm originating from histiocytic cell clones. The lesions can occur in nodal or extranodal sites. A minority of cases present as unique cutaneous lesions. The definitive diagnosis is made by immunohistochemistry. The treatment depends on the severity of the disease. Herein, we report a case of histiocytic sarcoma in a 65-year-old female presenting with subcutaneous swellings and ulcerated coalescing nodules on the forearms and thighs with metastasis to the lung and treated with systemic chemotherapy.
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