Lee Kyung Ho, Kim Jung Eun, Cho Baik Kee, Kim Yu Chan, Park Chul Jong
Department of Dermatology, College of Medicine, The Catholic University of Korea, 2 Sosa-Dong, Wonmi-Gu, Pucheon-Si, Kyunggi-Do, Korea.
Acta Derm Venereol. 2008;88(1):43-6. doi: 10.2340/00015555-0322.
Patients with the autosomal-dominant form of multiple familial trichoepithelioma develop numerous tumours on the face, neck and upper trunk, beginning in childhood. Malignant transformation of such lesions is quite rare; only one case of "malignant trichoepithelioma" has been reported previously, inferring pilomatrix carcinoma on a histological observation. We report here the case of a patient who developed a malignant neoplasm in a long-standing trichoepithelioma lesion on her buttock. Histopathology revealed a transformation zone between the trichoepithelioma and a malignant tumour mass. This case also showed several features of a malignant neoplasm of trichoblastic origin.
患有常染色体显性遗传型多发性家族性毛发上皮瘤的患者从儿童期开始,在面部、颈部和上躯干出现大量肿瘤。此类病变的恶性转化非常罕见;此前仅报告过一例“恶性毛发上皮瘤”,经组织学观察推断为毛母质癌。我们在此报告一例患者,其臀部长期存在的毛发上皮瘤病变发生了恶性肿瘤。组织病理学显示毛发上皮瘤与恶性肿瘤团块之间的转化区。该病例还表现出一些毛母质源性恶性肿瘤的特征。