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[阴茎恶性纤维组织细胞瘤]

[Malignant fibrous histiocytoma of the penis].

作者信息

Crisman G, Margiotta G, Calabresi M, Discepoli S, Leocata P

机构信息

Pathology Unit, University of L'Aquila, Loc. Vetoio Coppito 2, 67100, L'Aquila, Italien,

出版信息

Pathologe. 2015 Jul;36(4):385-8. doi: 10.1007/s00292-015-0036-9.

Abstract

According to the most recent World Health Organization (WHO) guidelines a diagnosis of malignant fibrous histiocytoma (MFH) should be made only for lesions composed of tumor cells without evidence of a specific line of differentiation. This is therefore a diagnosis by exclusion which is why the name of undifferentiated high-grade pleomorphic sarcoma (UPS) should be preferred. Soft tissue sarcomas currently have an incidence in all body regions of approximately 20 cases per 1 million inhabitants per year. Soft tissue tumors of the penis represent approximately 5 % of all penile tumors and the incidence of penile sarcomas is estimated to be approximately 0.6-1 case per 100,000 patients. Only seven cases have so far been reported in the literature. This article describes the case of a 61-year-old Caucasian male who presented with a painless mass sited in the upper part of the corpus cavernosa. An incisional biopsy with a subsequent investigation using an extensive immunohistochemical panel were performed and a high-grade undifferentiated pleomorphic sarcoma or pleomorphic storiform MFH was diagnosed. In addition to the case report a literature review is presented to elaborate the discussion on the differential diagnoses of these kinds of lesions.

摘要

根据世界卫生组织(WHO)的最新指南,只有在肿瘤细胞组成的病变中,且无特定分化谱系证据时,才能诊断为恶性纤维组织细胞瘤(MFH)。因此,这是一种排除性诊断,这就是为什么应优先使用未分化高级别多形性肉瘤(UPS)这一名称的原因。目前,软组织肉瘤在身体所有部位的发病率约为每年每100万居民中有20例。阴茎软组织肿瘤约占所有阴茎肿瘤的5%,阴茎肉瘤的发病率估计约为每10万名患者中有0.6 - 1例。迄今为止,文献中仅报道了7例。本文描述了一名61岁白种男性的病例,该患者阴茎海绵体上部出现无痛性肿块。进行了切开活检,并随后使用广泛的免疫组化检测进行了进一步检查,诊断为高级别未分化多形性肉瘤或多形性席纹状MFH。除了病例报告外,还进行了文献综述,以详细阐述关于这类病变鉴别诊断的讨论。

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