Large functioning Childhood adrenocortical carcinoma (Case report)

Authors

  • Jinan A. Jabbar The national center for early detection of cancer, Medical city.
  • Qusai A. Fahad Baghdad Teaching hospital, Medical city

DOI:

https://doi.org/10.32007/jfacmedbagdad.554597

Keywords:

paediatric adrenocortical tumor, functioning adrenocortical carcinoma.

Abstract

We describe a large functioning non metastasizing ACC in 8 years old boy who presented with a history of precocious puberty noticed by his parents since 3 months .Ultrasound of the abdomen showed a large well defined right suprarenal mass with calcification and necrosis . MRI  showed  the mass to be hypojntense to liver on T1 and   hyperintense  to liver on T2, and  dynamic CT scan revealed a large hetrogenous  enhancing right suprarenal mass with calcification and necrosis , clear chest .Histopathology done after surgical removal reveal adrenocortical carcinoma,so we recommend to do an abdominal ultrasound to any child with precocious puberty because it is easy,cheap and non invasive , if any suprarenal mass found it should be further characterized by MRI and  dynamic conontrast enhanced CT to determine its respectability

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Published

02.01.2014

How to Cite

1.
Jabbar JA, Fahad QA. Large functioning Childhood adrenocortical carcinoma (Case report). J Fac Med Baghdad [Internet]. 2014 Jan. 2 [cited 2024 Nov. 24];55(4):390-2. Available from: https://iqjmc.uobaghdad.edu.iq/index.php/19JFacMedBaghdad36/article/view/597

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