| Literature DB >> 28557715 |
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.Entities:
Mesh:
Year: 2017 PMID: 28557715 DOI: 10.1542/peds.2016-0170
Source DB: PubMed Journal: Pediatrics ISSN: 0031-4005 Impact factor: 7.124