臀部转移性肌圆细胞脂肪肉瘤:病例报告。

IF 0.9 Q4 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH
Pan African Medical Journal Pub Date : 2024-06-13 eCollection Date: 2024-01-01 DOI:10.11604/pamj.2024.48.56.40400
Niare Ndour, Mamadou Sarr, Assane Diop, Mamadou Diouldé Kanté, Coumba Ndiaye, Astou Diouf, Fatou Diagne, Moussa Diallo, Fatimata Ly
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引用次数: 0

摘要

脂肪肉瘤是一种罕见的原始间充质肿瘤,以脂肪组织为生,好发于大腿。我们报告了一起臀部脂肪肉瘤的病例。一名 56 岁的男子右臀部出现肿瘤已有 2 年之久。检查发现右臀部外上象限有一个炎性溃疡肿瘤,大小约 8 厘米。同时伴有双侧腹股沟腺病。诊断假设为:鳞状细胞癌、皮肤淋巴瘤和皮肤转移瘤。解剖检查证实了肌圆细胞脂肪肉瘤的诊断。扩展检查结果显示,继发胸膜肺癌、肝癌、皮肤癌和淋巴结肿瘤的可能性较大。患者接受了阿霉素-卡铂方案化疗。第一个化疗疗程结束几周后,病情迅速恶化,最终死亡。在任何臀部溃疡性肿瘤面前都应引起重视。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Metastatic myxoid round cell liposarcoma of the buttock: a case report.

Liposarcoma is a rare primitive mesenchymal tumor, developed at the expense of adipose tissue and with a preferential location in the thigh. We report an observation of liposarcoma in the buttock. A 56-year-old man, presented with a tumor of the right buttock for 2 years. Examination revealed an inflammatory, ulcerated tumor in the upper-external quadrant of the right buttock, measuring about 8 cm. Bilateral inguinal adenopathies were associated. The diagnostic hypotheses were: a squamous cell carcinoma, a cutaneous lymphoma, and cutaneous metastases. An anatomical examination confirmed the diagnosis of myxoid round-cell liposarcoma. The extension work-up appeared compatible with secondary pleuropulmonary, hepatic, cutaneous, and lymph node neoplastic localizations. The patient was treated with chemotherapy with the Adriamycin-carboplatin protocol. The evolution was rapidly fatal after a few weeks after the first course of chemotherapy. It should be evoked in front of any ulcerated tumor of the buttock.

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来源期刊
Pan African Medical Journal
Pan African Medical Journal PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH-
CiteScore
1.80
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发文量
691
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