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Amyloidosis cutis dyschromica.

Author(s)
Ranju Choudhary Department of Skin, VD and Leprosy, Rajendra Institute of Medical Sciences, Bariatu, Ranchi, India
V. Madhu Sudhanan Department of Skin, VD and Leprosy, Rajendra Institute of Medical Sciences, Bariatu, Ranchi, India
Mritunjay Kumar Department of Skin, VD and Leprosy, Rajendra Institute of Medical Sciences, Bariatu, Ranchi, India
Shyam Sundar Chaudhary Department of Skin, VD and Leprosy, Rajendra Institute of Medical Sciences Bariatu, Ranchi, India
Abstract
Amyloidosis cutis dyschromica (ACD) is a rare form of cutaneous amyloidosis; characterized by generalized; asymptomatic hyperpigmentation intermingled with several hypopigmented spots without papulation; atrophy and telangiectasia. Its onset usually begins before puberty. We hereby describe two female siblings of ACD belonging to tribal groups with no systemic involvement. This condition should be considered as a separate entity and need to be differentiated from other variants of primary cutaneous amyloidosis
Publication Details
Page(s) 319-321
DOI DOI not available
Published Journal: Journal of Pakistan Association of Dermatologists, Volume: 25, Issue: 4, Year: 2015

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