scholarly journals ACTH-independent Cushing's syndrome due to bilateral adrenocortical adenoma: A case report

2021 ◽  
Vol 16 (11) ◽  
pp. 3168-3171
Author(s):  
Majd Sharaf ◽  
Rama Al-Saqqa ◽  
Mouhammad Kourabi
2020 ◽  
Vol 20 (1) ◽  
Author(s):  
Shaohua Li ◽  
Chen Yang ◽  
Jing Fan ◽  
Yao Yao ◽  
Xiaomei Lv ◽  
...  

2003 ◽  
Vol 17 (5) ◽  
pp. 403-406 ◽  
Author(s):  
Akiko Shimizu ◽  
Noboru Oriuchi ◽  
Yoshito Tsushima ◽  
Tetsuya Higuchi ◽  
Jun Aoki ◽  
...  

2007 ◽  
Vol 13 (2) ◽  
pp. 153-158 ◽  
Author(s):  
David Kem ◽  
Jordan Metcalf ◽  
Ana Cornea ◽  
Monica Dunnam ◽  
Alice Engelbrecht ◽  
...  

2019 ◽  
Vol 66 (2) ◽  
pp. 175-180
Author(s):  
Kewei Wang ◽  
Fuqiang Liu ◽  
Chuanlong Wu ◽  
Yan Liu ◽  
Lin Qi ◽  
...  

1970 ◽  
Vol 22 (1) ◽  
pp. 142-143
Author(s):  
M Nowshad Ali ◽  
S Hoq Miah ◽  
M Meharunnesa ◽  
SM Badruddoza ◽  
Mushtaque Ahmed

Adrenocortical carcinoma is an uncommon tumour in the pediatric population. Account for only a small fraction of pediatric adrenal tumour. Most tumors in children are functional, and virilization is by far the most common presenting symptom, followed by Cushing's syndrome and precocious puberty. All patients with suspected adrenocortical carcinoma should be carefully evaluated for signs and symptoms of hormonal syndromes. DOI: 10.3329/taj.v22i1.5039 TAJ 2009; 22(1): 142-143


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