Central precocious puberty after resection of a virilising adrenocortical oncocytic tumour

被引:1
|
作者
Madi, Lee Rima [1 ]
Fisch Shvalb, Naama [1 ,2 ]
Sade Zaltz, Chen [1 ,3 ]
Levy-Shraga, Yael [1 ,4 ]
机构
[1] Tel Aviv Univ, Sackler Fac Med, Tel Aviv, Israel
[2] Schneider Childrens Med Ctr, Jesse & Sara Lea Shafer Inst Endocrinol & Diabet, Petah Tiqwa, Israel
[3] Rabin Med Ctr, Dept Pathol, Beilinson Campus, Petah Tiqwa, Israel
[4] Edmond & Lily Safra Childrens Hosp, Sheba Med Ctr, Pediat Endocrinol & Diabet Unit, Ramat Gan, Israel
关键词
adrenal disorders; paediatrics; CONGENITAL ADRENAL-HYPERPLASIA; NEOPLASMS; UPDATE; CHILD;
D O I
10.1136/bcr-2020-239562
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Adrenocortical oncocytic tumours are a histological subtype of adrenal neoplasms with a distinctive morphological appearance. Since these tumours are composed of cells of the adrenal cortex, they may act as functional tumours with excess hormone production. They may cause Cushing's syndrome, inappropriate virilisation or precocious puberty. Though rare during childhood, adrenocortical oncocytic tumours should be suspected in a child with peripheral precocious puberty and marked elevation of dehydroepiandrosterone sulfate levels. We describe a 6-year girl who presented with peripheral precocious puberty due to a functional adrenocortical oncocytic tumour. Three months after tumour removal, she developed true central precocious puberty. This report highlights that peripheral precocious puberty may trigger central precocious puberty, particularly after resolution of the underlying cause of the peripheral precocious puberty.
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页数:4
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