| Literature DB >> 20548911 |
Jong Wook Park1, Sun Namkoong, Jimin Chung, Kyung Eun Jung, Sang A Oh, Yong Woo Cinn, Myung Hwa Kim.
Abstract
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.Entities:
Keywords: Eccrine spiradenoma; Neurofibromatosis
Year: 2010 PMID: 20548911 PMCID: PMC2883423 DOI: 10.5021/ad.2010.22.2.191
Source DB: PubMed Journal: Ann Dermatol ISSN: 1013-9087 Impact factor: 1.444