Literature DB >> 28557715

Amyloidosis Cutis Dyschromica, a Rare Cause of Hyperpigmentation: A New Case and Literature Review.

Oya Kuseyri1, Dorothea Haas2, Nina Lang3, Knut Schäkel3, Markus Bettendorf2.   

Abstract

Amyloidosis cutis dyschromica is a rare form of primary cutaneous amyloidosis without systemic involvement and characterized by asymptomatic, progressive hyper- and hypopigmentation. We present the first case of a patient with amyloidosis cutis dyschromica diagnosed previously elsewhere as having Addison disease with generalized hyperpigmentation of the skin. This case suggests that in patients presenting with asymptomatic cutaneous dyschromia a skin biopsy for histopathological examination should be considered.
Copyright © 2017 by the American Academy of Pediatrics.

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Year:  2017        PMID: 28557715     DOI: 10.1542/peds.2016-0170

Source DB:  PubMed          Journal:  Pediatrics        ISSN: 0031-4005            Impact factor:   7.124


  1 in total

1.  Case Report: Amyloidosis Cutis Dyschromica: Dermoscopy and Reflectance Confocal Microscopy and Gene Mutation Analysis of a Chinese Pedigree.

Authors:  Hui Wang; Zhenyu Zhong; Xiuli Wang; Liyun Zheng; Yifan Wang; Shan Wang; Siqi Liu; Hui Li; Ze Guo; Min Gao
Journal:  Front Med (Lausanne)       Date:  2021-12-01
  1 in total

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