Addison´s disease in a young child: A rare entity in children

Authors

  • Sadaf Amin Fatima Jinnah Medical University/ Sir Ganga Ram Hospital, Lahore
  • Zain Ali Raza Fatima Jinnah Medical University/ Sir Ganga Ram Hospital, Lahore
  • Nadia Ali Azfar Fatima Jinnah Medical University/ Sir Ganga Ram Hospital, Lahor
  • Muhammad Nadeem Fatima Jinnah Medical University/ Sir Ganga Ram Hospital, Lahore

DOI:

https://doi.org/10.66344/jpad.v30i2.1399

Keywords:

Addison´s disease, rare entity

Abstract

Addison's disease is an adrenocortical insufficiency due to the dysfunction or destruction of the entire adrenal gland. The disease usually manifests when 90% or more of both adrenal cortices are dysfunctional or destroyed affecting both glucocorticoid and mineralocorticoid functions. The morbidity and mortality associated with Addisons disease is relatively high due to delay in diagnosis and initiation of therapy. Here, we report a case of a seven years old child who presented to us with diffuse hyperpigmentation of the body, body flexures, palmar creases and mucosae. He was diagnosed with Addison´s disease, which is indeed a rare entity. In addition, this case report will also enhance the importance of cutaneous examination in suspecting Addison´s disease.

References

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Published

30.09.2020

Issue

Section

Case Reports

How to Cite

1.
Addison´s disease in a young child: A rare entity in children. J Pak Assoc Dermatol [Internet]. 2020 Sep. 30 [cited 2026 Jul. 22];30(2):359-62. Available from: https://www.jpad.com.pk/index.php/jpad/article/view/1399