Park Jong Wook, Namkoong Sun, Chung Jimin, Jung Kyung Eun, Oh Sang A, Cinn Yong Woo, Kim Myung Hwa
Department of Dermatology, College of Medicine, Dankook University, Cheonan, Korea.
Ann Dermatol. 2010 May;22(2):191-3. doi: 10.5021/ad.2010.22.2.191. Epub 2010 May 18.
Neurofibromatosis is a systemic hereditary disorder with varied manifestations in bone, soft tissue, the nervous system and skin. Cutaneous manifestations of neurofibromatosis are characterized by café-au-lait macules, multiple neurofibromas, Lisch nodules and intertriginous freckling. Some benign or malignant tumors such as juvenile xanthogranuloma, pheochromocytoma, and malignant melanoma can accompany neurofibromatosis. But, in the English literature, no case of eccrine spiradenoma associated with neurofibromatosis has been reported. Eccrine spiradenoma is a benign uncommon neoplasm of skin adnexa. It presents as a painful, slow-growing and solitary nodule on the head or upper trunk. Here, we report a rare case of eccrine spiradenoma in a patient with neurofibromatosis.
神经纤维瘤病是一种全身性遗传性疾病,在骨骼、软组织、神经系统和皮肤方面有多种表现。神经纤维瘤病的皮肤表现特征为咖啡斑、多发性神经纤维瘤、Lisch结节和间擦部位雀斑。一些良性或恶性肿瘤,如幼年性黄色肉芽肿、嗜铬细胞瘤和恶性黑色素瘤可伴发神经纤维瘤病。但是,英文文献中尚未报道过与神经纤维瘤病相关的小汗腺螺旋腺瘤病例。小汗腺螺旋腺瘤是一种少见的皮肤附属器良性肿瘤。它表现为头部或上躯干的疼痛性、生长缓慢的孤立结节。在此,我们报告1例神经纤维瘤病患者伴发小汗腺螺旋腺瘤的罕见病例。