Indian Journal of Dermatopathology and Diagnostic Dermatology

CASE REPORT
Year
: 2019  |  Volume : 6  |  Issue : 1  |  Page : 45--47

Amyloidosis cutis dyschromica: A rare dyschromic pigmentary disorder


Kuldeep Verma1, Reena Kumari Sharma1, Anchana Gulati2, Mudita Gupta1 
1 Department of Dermatology, Venereology and Leprosy, Indira Gandhi Medical College, Shimla, Himachal Pradesh, India
2 Department of Pathology, Indira Gandhi Medical College, Shimla, Himachal Pradesh, India

Correspondence Address:
Dr. Mudita Gupta
Department of Dermatology, Venereology and Leprosy, Indira Gandhi Medical College, Shimla, Himachal Pradesh
India

Primary cutaneous amyloidosis (PCA) is the deposition of amyloid proteins in the skin without systemic involvement. Amyloidosis cutis dyschromica (ACD) is a rare variant of PCA with onset typically in early childhood or at a prepubertal age. It is more common in the Asian and Southeast Asian people. Clinically it manifests as asymptomatic diffuse hyperpigmentation interspersed with hypopigmented spots without papulation. Histologically, small foci of amyloid closely under the epidermis are seen. There are only few case reports in the literature of this rarer variant. We report a case of a 32-year-old male presenting as dyschromatosis with a prepubertal onset and histopathological evidence of intradermal deposits in the upper dermis which was confirmed on Congo red staining and hence was diagnosed as a case of ACD.


How to cite this article:
Verma K, Sharma RK, Gulati A, Gupta M. Amyloidosis cutis dyschromica: A rare dyschromic pigmentary disorder.Indian J Dermatopathol Diagn Dermatol 2019;6:45-47


How to cite this URL:
Verma K, Sharma RK, Gulati A, Gupta M. Amyloidosis cutis dyschromica: A rare dyschromic pigmentary disorder. Indian J Dermatopathol Diagn Dermatol [serial online] 2019 [cited 2019 Dec 16 ];6:45-47
Available from: http://www.ijdpdd.com/article.asp?issn=WKMP-0052;year=2019;volume=6;issue=1;spage=45;epage=47;aulast=Verma;type=0