Angiokeratoma corporis diffusum without systemic features in a young Kashmiri female: a rare occurrence

Authors

  • Iffat Hassan Postgraduate Department of Dermatology, STD & Leprosy, Government Medical College Srinagar (University of Kashmir), J&K, India
  • Parvaiz Anwar Rather Postgraduate Department of Dermatology, STD & Leprosy, Government Medical College Srinagar (University of Kashmir), J&K, India
  • Saima Aleem Postgraduate Department of Dermatology, STD & Leprosy, Government Medical College Srinagar (University of Kashmir), J&K, India

DOI:

https://doi.org/10.66344/jpad.v23i3.334

Keywords:

Angiokeratoma, angiokeratoma corporis diffusum, lysosomal enzyme deficiency

Abstract

Angiokeratoma corporis diffusum (ACD) is a variety of angiokeratoma, characterized by diffuse cutaneous hyperkeratotic vascular lesions. ACD is usually associated with many lysosomal enzyme deficiencies, though it is not a rule. It is associated with systemic features along with skin lesions. It may also present as isolated cutaneous form. X-linked recessive form usually manifests in males and females act as carriers. We report a case of ACD without systemic features in a young Kashmiri female.

References

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Published

15.12.2016

Issue

Section

Case Reports

How to Cite

1.
Angiokeratoma corporis diffusum without systemic features in a young Kashmiri female: a rare occurrence. J Pak Assoc Dermatol [Internet]. 2016 Dec. 15 [cited 2026 Aug. 2];23(3):327-30. Available from: https://www.jpad.com.pk/index.php/jpad/article/view/334