1.
JPAD-Journal of Pakistan Association of Dermatologists. 2015; 25 (4): 334-336
in English
| IMEMR
| ID: emr-181155
ABSTRACT
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.