Wachter-Giner Tina, Bieber Imke, Warmuth-Metz Monika, Bröcker Eva-B, Hamm Henning
Department of Dermatology, University of Wuerzburg, Germany.
Pediatr Dermatol. 2009 Jan-Feb;26(1):75-8. doi: 10.1111/j.1525-1470.2008.00827.x.
Pilomatricomas are benign skin tumors originating from hair follicle matrix cells. In 2% to 3.5% of cases they occur in multiplicity and then may be associated with genetic diseases, such as myotonic dystrophy Curschmann-Steinert, familial adenomatous polyposis (Gardner syndrome), and Rubinstein-Taybi syndrome. A 15-year-old boy treated with temozolomide and oxcarbazepine for gliomatosis cerebri with symptomatic epilepsy developed four firm cutaneous nodules on his face and right upper arm in the course of 1 year. All four tumors were excised under local anesthesia. Histological examination confirmed the clinical diagnosis of pilomatricomas. This is the first published case of a patient suffering from gliomatosis cerebri and developing multiple pilomatricomas. Whether this observation represents a new association or is a mere coincidence cannot be clarified at present.
毛母质瘤是起源于毛囊基质细胞的良性皮肤肿瘤。在2%至3.5%的病例中,它们会多发,进而可能与遗传性疾病相关,如强直性肌营养不良(库施曼-施泰纳特病)、家族性腺瘤性息肉病(加德纳综合征)和鲁宾斯坦-泰比综合征。一名15岁男孩因患有伴有症状性癫痫的大脑胶质瘤病而接受替莫唑胺和奥卡西平治疗,在1年的病程中,其面部和右上臂出现了4个坚实的皮肤结节。所有4个肿瘤均在局部麻醉下切除。组织学检查证实了毛母质瘤的临床诊断。这是首例关于患有大脑胶质瘤病并发生多发毛母质瘤患者的报道。目前尚无法明确这一观察结果是代表一种新的关联还是仅仅是巧合。