Amyloidosis cutis dyschromia: a case report

Authors

  • Anup Kumar Tiwary
  • Dharmender Kumar Mishra
  • Yashwant Anant Lal
  • Shyam Sundar Chaudhary

Keywords:

Amyloidosis cutis dyschromia, hyperpigmentation, hypopigmented macules, amyloid deposits

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.

References

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Published

2016-11-26

How to Cite

1.
Tiwary AK, Mishra DK, Lal YA, Chaudhary SS. Amyloidosis cutis dyschromia: a case report. J Pak Assoc Dermatol [Internet]. 2016Nov.26 [cited 2024Dec.7];25(4):334-6. Available from: https://www.jpad.com.pk/index.php/jpad/article/view/158

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