A rare case of isolated Cushing syndrome in a 3-month-old boy

被引：0

作者：

Garge, Saurabh ^{[1
]}

Bawa, Monika ^{[1
]}

Kanojia, Ravi P. ^{[1
]}

Gupta, Kirti ^{[2
]}

Rao, Kattragadda Laxmi Narain ^{[1
]}

机构：

[1] Postgrad Inst Med Educ & Res PGIMER, Dept Pediat Surg, Chandigarh 160012, India

[2] Postgrad Inst Med Educ & Res PGIMER, Dept Histopathol, Chandigarh 160012, India

来源：

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM | 2013年 / 26卷 / 5-6期

关键词：

adrenocortical carcinoma; Cushing syndrome; virilizing tumors; ADRENAL-CORTICAL TUMORS; ADRENOCORTICAL CARCINOMA; COMPUTED-TOMOGRAPHY; CHILDHOOD; CHILDREN; POPULATION; EXPERIENCE; ULTRASOUND; NEOPLASMS;

D O I：

10.1515/JPEM.2011.343

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Adrenocortical carcinoma (ACC) is a rare malignancy in children. Most of these are endocrinologically active tumors, with virilizing features being typically dominant. Its presentation with isolated Cushing syndrome is rare. We report a 3-month-old infant with Cushing syndrome without the clinical features of androgen or mineralocorticoid excess consequently diagnosed with ACC. We discuss the different presentations, diagnosis, and management of this rare tumor with a rarer presentation.

引用

页码：599 / 603

页数：5

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