Amyloidosis Cutis Dyschromica, a Rare Cause of Hyperpigmentation: A New Case and Literature Review.
case_report · Level V
Where this comes from
- Record sourced from PubMed, PMID 28557715.
- Also identified by DOI 10.1542/peds.2016-0170.
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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.
Medical subject headings
- Amyloidosis, Familial
- Hyperpigmentation
- Skin
- Skin Diseases, Genetic