Adrenocortical Tumor In Children – Report of a Case

Authors

  • Mansoor Mahmood Dept. Pediatric Surgery
  • Nadeem Akhtar Department of Pediatric Surgery
  • Saqib Ismail Department of Pediatric Surgery
  • Sheema . Department of Pediatric Surgery
  • Yazeed Owiwii Department of Pediatric Surgery

Keywords:

Adrenocortical Carcinoma in Children, Virilization, Adrenal Tumors

Abstract

Abstract
Adrenocortical carcinoma in childhood is a rare, potentially fatal disease.Adrenocortical carcinoma has a bimodal age distribution
with cases clustering in children under 6, and in adults 30–40years old. We are presenting a case of 2 years old girl
who presented with symptoms of virilization. She was operated for the adrenal mass. A diagnosis of adrenocortical carcinoma
was rendered.

Downloads

Published

2018-11-15

Issue

Volume.10, Issue (July-December, 2012)

Section

Original article

License

Readers may “Share-copy and redistribute the material in any medium or format” and “Adapt-remix, transform, and build upon the material”. The readers must give appropriate credit to the source of the material and indicate if changes were made to the material. Readers may not use the material for commercial purpose. The readers may not apply legal terms or technological measures that legally restrict others from doing anything the license permits.

How to Cite

1.
Mahmood M, Akhtar N, Ismail S, . S, Owiwii Y. Adrenocortical Tumor In Children – Report of a Case. Int J Pathol [Internet]. 2018 Nov. 15 [cited 2024 May 8];:82-5. Available from: https://jpathology.com/index.php/OJS/article/view/109

Most read articles by the same author(s)