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CASE REPORT
Year : 2013  |  Volume : 4  |  Issue : 4  |  Page : 344-346

Amyloidosis cutis dyschromica


1 Department of Dermatology, Venereology and Leprology, PSG Institute of Medical Sciences and Research (PSG IMSR), Coimbatore, Tamil Nadu, India
2 Department of Pathology, PSG Institute of Medical Sciences and Research (PSG IMSR), Coimbatore, Tamil Nadu, India

Correspondence Address:
Reena Rai
Department of Dermatology, PSG Institute of Medical Sciences and Research (PSG IMSR), Peelamedu, Coimbatore, Tamil Nadu
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/2229-5178.120678

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Amyloidosis cutis dyschromica is a very rare form of primary cutaneous amyloidosis characterized by prepubertal onset of hyper and hypopigmented spots and amyloid deposits in the papillary dermis. We report a case of a 26 year old female with amyloidosis cutis dyschromica who presented with dyschromic skin since birth.


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