Amyloidosis cutis dyschromica, a rare cause of hyperpigmentation: a new case and literature review
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 Ad...
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| Hauptverfasser: | , , , , |
|---|---|
| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
May 2017
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| In: |
Pediatrics
Year: 2017, Jahrgang: 139, Heft: 5 |
| ISSN: | 1098-4275 |
| DOI: | 10.1542/peds.2016-0170 |
| Online-Zugang: | Verlag, Volltext: http://dx.doi.org/10.1542/peds.2016-0170 Verlag, Volltext: http://pediatrics.aappublications.org/content/139/5/e20160170 
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| Verfasserangaben: | Oya Kuseyri, Dorothea Haas, Nina Lang, Knut Schäkel, Markus Bettendorf |
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| 520 | |a 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. | ||
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