ea0085p51 | Adrenal 2 | BSPED2022
Dimarsha de Silva U. A .M.
, Suntharesan Jananie
, Somathilaka Mahendra
, Liyanage Janath
, A. Hemali de Silva M.
Background: Adrenocortical carcinoma in childhood is a rare tumour which accounts for about 0.2% of all paediatric malignancies. Affected children usually present with virilization, cushingoid features, and/or mineralocorticoid excess. We present a boy with adrenal carcinoma presented with virilization and unusually suppressed cortisol at initial presentation.Case report: A two-year-old boy presented with pubic hair, acne, and increased penile growth wit...