A rare type of primary cutaneous amyloidosis: amyloidosis cutis dyschromica
A rare type of primary cutaneous amyloidosis: amyloidosis cutis dyschromica
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DOI：
10.1111/j.1365-4632.2009.04394.x
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发表时间：
2010-12-01
影响因子：
3.6
通讯作者：
de Silva, M. V. C.
中科院分区：
文献类型：
--
作者：
Madarasingha, N. P.;Satgurunathan, K.;de Silva, M. V. C.
本文介绍了一位36岁男性的病例研究，他在童年时期就开始出现泛发性斑点状无症状以及色素亢进和色素减退。患者也有多发性苔藓样丘疹，但没有表现出光敏、起泡或身材矮小。它说，目前还没有确切的病因，但鉴别诊断包括遗传性泛发性色素异常症。它讨论了一种皮肤淀粉样变性。
The article presents a case study of a 36-year old male who was presented with generalized mottled asymptomatic as well as hyper and hypopigmented macules, which started during his childhood. The patient also had multiple lichenoid papules but exhibited no photosensitivity, blistering eruption, or short stature. It says that there was no exact etiology of the disease but differential diagnosis included dyschromatosis universalis hereditaria. It discusses a type of cutaneous amyloidosis.