厚皮性骨膜病：综合征的完全型。
Pachydermoperiostosis: the complete form of the syndrome.
作者信息
Guerini Marina Besen, Barbato Mariana Tremel, Sá Naiana Bittencourt de, Nunes Daniel Holthausen, Zeni Paulo Roberto
机构信息
Dermatology Department, Teaching Hospital, Federal University of Santa Catarina, Florianópolis, Santa Catarina, Brazil.
出版信息
An Bras Dermatol. 2011 May-Jun;86(3):582-4. doi: 10.1590/s0365-05962011000300027.
Pachydermoperiostosis is a rare genodermatosis with various clinical presentations that include pachydermia (thickening of the skin), finger clubbing and periostitis. Its pathogenesis is uncertain and the condition affects mainly men. This report describes the case of a patient with typical, exuberant skin manifestations and classic radiological findings of this syndrome in its complete form.
厚皮性骨膜病是一种罕见的遗传性皮肤病，有多种临床表现，包括皮肤增厚、杵状指和骨膜炎。其发病机制尚不清楚，主要影响男性。本报告描述了一例具有典型、丰富皮肤表现和该综合征完整形式的经典影像学表现的患者病例。
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