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阴茎头多形性恶性纤维组织细胞瘤/未分化多形性肉瘤

Pleomorphic malignant fibrous histiocytoma/undifferentiated pleomorphic sarcoma of the glans penis.

作者信息

Seo Ill Young, Oh Tae Hoon, Chuluun Sarantulga, Choi Keum Ha

机构信息

Departments of Urology and Pathology, Institute of Wonkwang Medical Science, Wonkwang University School of Medicine, Iksan, Korea;

Department of General Surgery, National Cancer Center, Ulaanbaatar, Mongolia.

出版信息

Can Urol Assoc J. 2013 Nov-Dec;7(11-12):E823-5. doi: 10.5489/cuaj.1052.

DOI:10.5489/cuaj.1052
PMID:24475005
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3879732/
Abstract

Primary sarcoma of the penis has an extremely low incidence, and its diagnosis and treatment are unclear. A 55-year-old man presented with an oval-shaped mass of the glans penis, which was treated by a wide excision. The pathologic result revealed an undifferentiated high-grade sarcoma, which was diagnosed as a pleomorphic malignant fibrous histiocytoma/undifferentiated pleomorphic sarcoma based on the World Health Organization classification. There was no recurrence at the12-months postoperative follow-up.

摘要

阴茎原发性肉瘤的发病率极低,其诊断和治疗尚不明确。一名55岁男性患者阴茎头出现椭圆形肿物,接受了广泛切除治疗。病理结果显示为未分化高级别肉瘤,根据世界卫生组织分类诊断为多形性恶性纤维组织细胞瘤/未分化多形性肉瘤。术后12个月随访未发现复发。

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引用本文的文献

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Primary undifferentiated penile sarcoma in adolescence.青少年原发性未分化阴茎肉瘤。
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MFH classification: differentiating undifferentiated pleomorphic sarcoma in the 21st Century.黏液纤维肉瘤分类:21世纪未分化多形性肉瘤的鉴别
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