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JPAD-Journal of Pakistan Association of Dermatologists. 2015; 25 (4): 334-336
em Inglês | IMEMR | ID: emr-181155

RESUMO

Amyloidosis cutis dyschromia is a very rare variant of primary cutaneous amyloidosis clinically characterized by hyper- and hypopigmented/depigmented macules in generalized distribution. Diagnosis is based on histopathological demonstration of amyloid deposits in papillary dermis and its confirmation by Congo red staining. We hereby report a case of amyloidosis cutis dyschromia.

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