Amyloidosis cutis dyschromia: a case report. | [Journal of Pakistan Association of Dermatologists • 2015]

Author(s):

1. Anup Kumar Tiwary: Department of Dermatology, Venereology & Leprosy, Rajendra Institute of Medical Sciences, Ranchi, India

2. Dharmender Kumar Mishra: Department of Dermatology, Venereology & Leprosy, Rajendra Institute of Medical Sciences, Ranchi, India

3. Yashwant Anant Lal: Department of Dermatology, Venereology & Leprosy, Rajendra Institute of Medical Sciences, Bariatu, Ranchi, India

4. Shyam Sundar Chaudhary: Department of Dermatology, Venereology & Leprosy, Rajendra Institute of Medical Sciences, Ranchi, India

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 inpapillary dermis and its confirmation by Congo red staining. We hereby report a case of amyloidosis cutis dyschromia

Page(s): 334-346

DOI: DOI not available

Published: Journal: Journal of Pakistan Association of Dermatologists, Volume: 25, Issue: 4, Year: 2015

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