Uncommon Adrenal Tumors in Children and Adolescents

Author:

Ribeiro Raul C.1,Rodriguez-Galindo Carlos1,Pinto Emilia M.1,Zambetti Gerard P.1,Figueiredo Bonald C.2

Affiliation:

1. St Jude Children's Research Hospital; Memphis Tennessee USA

2. Pelé Pequeno Príncipe Research Institute; Faculdades Pequeno Príncipe; Curitiba Paraná Brazil

Publisher

John Wiley & Sons, Ltd

Reference130 articles.

1. General melasma and short hair over the entire body of a child of three years, with conversion of the left supra-renal capsule into a large malignant tumour; the external organs of generation resembling those of adult life;St George's Hospital;Lancet,1865

2. The suprarenal cortical syndrome with presentation of ten cases;Walters;Ann Surg,1934

3. Adrenocortical carcinoma in children: a study of 40 cases;Ribeiro;J Clin Oncol,1990

4. Clinical and outcome characteristics of children with adrenocortical tumors: a report from the International Pediatric Adrenocortical Tumor Registry;Michalkiewicz;J Clin Oncol,2004

5. Predictors of survival in pediatric adrenocortical carcinoma: a Surveillance, Epidemiology, and End Results (SEER) program study;McAteer;J Pediatr Surg,2013

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