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伴有向基底细胞癌恶性转化的非孤立性巨大肛周毛发上皮瘤:1例报告并文献复习

Nonsolitary giant perianal trichoepithelioma with malignant transformation into basal cell carcinoma: report of a case and review of the literature.

作者信息

Martinez Carlos Augusto Real, Priolli Denise Gonçalves, Piovesan Helenice, Waisberg Jaques

机构信息

Department of General Surgery of the Faculty of Medicine of Universidade São Francisco, Bragança Paulista, Sao Paulo, Brazil.

出版信息

Dis Colon Rectum. 2004 May;47(5):773-7. doi: 10.1007/s10350-003-0104-8. Epub 2004 Apr 13.

Abstract

Trichoepitheliomas are benign cutaneous tumors that originate from hair follicles and present in two clinical forms. Multiple trichoepithelioma has autosomal transmission and is dominant as a result of the loss of heterozygosity in the 9p21 region, whereas the giant form is solitary, nonhereditary, and rarely affects the perianal region. Diagnostic differentiation from basal cell carcinoma presents notable difficulty, and the use of immunohistochemical studies often is necessary for correct differentiation. The concomitant presence of giant solitary trichoepithelioma and basal cell carcinoma raises the question of whether there is the possibility of malignant transformation, or if it is simply an encounter between the two types of neoplasia. The objective of the present study was to report on a patient who had the two clinical forms of trichoepithelioma (multiple trichoepithelioma and giant solitary trichoepithelioma) in the perianal region, without hereditary antecedents. In this case, the transformation of the largest-sized lesion into basal cell carcinoma was observed. The lesions were studied by means of histopathologic and immunohistochemical studies to investigate the bcl-2 oncogene. The tissue expression characteristics for bcl-2 and the histopathologic examination allowed the diagnosis of multiple trichoepithelioma in the smaller lesions and nonsolitary giant trichoepithelioma with malignant transformation into basal cell carcinoma in the largest-sized lesion. After surgical excision and adjuvant radiotherapy, the patient is now asymptomatic, without signs of relapse, eight months after the surgery.

摘要

毛发上皮瘤是起源于毛囊的良性皮肤肿瘤,有两种临床形式。多发性毛发上皮瘤具有常染色体显性遗传,是9p21区域杂合性缺失的结果,而巨大型毛发上皮瘤是单发、非遗传性的,很少累及肛周区域。与基底细胞癌进行诊断鉴别存在显著困难,通常需要使用免疫组织化学研究来进行正确鉴别。巨大孤立性毛发上皮瘤与基底细胞癌同时存在,引发了是否存在恶性转化的可能性,或者这仅仅是两种肿瘤的偶然并存的问题。本研究的目的是报告一名肛周区域患有两种临床形式毛发上皮瘤(多发性毛发上皮瘤和巨大孤立性毛发上皮瘤)且无遗传病史的患者。在该病例中,观察到最大的病变转变为基底细胞癌。通过组织病理学和免疫组织化学研究对病变进行了研究,以调查bcl-2癌基因。bcl-2的组织表达特征和组织病理学检查使得较小病变诊断为多发性毛发上皮瘤,最大病变诊断为非孤立性巨大毛发上皮瘤伴恶性转化为基底细胞癌。手术切除并辅助放疗后,患者在术后八个月无症状,无复发迹象。

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