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Annals of Dermatology 2010 May; 22(2): 191~193
Annals of Dermatology 2010 May; 22(2): 191~193

A Case of Eccrine Spiradenoma in a Patient with Neurofibromatosis
Jong Wook Park, M.D., Sun Namkoong, M.D., Jimin Chung, M.D., Kyung Eun Jung, M.D., Sang A Oh, M.D.1, Yong Woo Cinn, M.D., Myung Hwa Kim, M.D.
Departments of Dermatology and 1Plastic Surgery, College of Medicine, Dankook University, Cheonan, Korea
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
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. (Ann Dermatol 22(2) 191∼193, 2010)
Annals of Dermatology 2010 May; 22(2): 191~193
Keyword : Eccrine spiradenoma, Neurofibromatosis
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