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Olmsted syndrome: a case report and review of literature
Authors:Tao Juan  Huang Chang-Zheng  Yu Nian-Wen  Wu Yan  Liu Ye-Qiang  Li Yan  Tian Jin  Yang Ling-Yun  Zhang Jing  Li Jia-Wen  Zhou You-Wen  Tu Ya-Ting
Affiliation:From 1Department of Dermatology, Affiliated Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China,;2Department of Dermatology, Affiliated Huiji Hospital of Hubei Professional and Technology College, Xiaogan, Hubei 432000, China, and;3Department of Dermatology and Skin Science, University of British Columbia, Vancouver, Canada
Abstract:We report a case of an 18-month-old boy with slightly whitened fingernails and toenails since birth. At the age of 100 days, he progressively developed bilateral palmoplantar keratoderma which resulted in painful walking and disabled grasping. Perianal keratotic plaques and perioral hyperkeratotic erythema could also be observed. Both fingernails and toenails were dystrophic. Scalp hairs were sparse, but total alopecia was no present. The histopathologic changes of the biopsy from the inner side of the right foot showed nonspecific changes, which mainly showed highly hyperkeratosis and acanthosis with slight superficial perivascular inflammatory infiltration. A clinical diagnosis of Olmsted syndrome was established according to the typical feature of the lesions, which is the presence of symmetrical palmoplantar keratoderma with periorificial keratotic plaques. We review the literature and present a summary of all reported cases to date.
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