Results 151 to 160 of about 1,645,101 (196)

Ultrasound Diagnosis of Giant Testicular Adrenal Residual Tumors: A Case Report and Literature Review. [PDF]

J Clin Ultrasound
Ge Y, Zhu H, Kong D, Wang Y, Mao L.
europepmc   +1 more source

Behind the Curtain: A Pediatric Dermoid Tumor Masquerading as Craniopharyngioma. [PDF]

Cureus
Stückrath A, Rivera F, Negri P.
europepmc   +1 more source

Feminizing Adrenocortical Carcinoma in Men: A Rare Cause of Persistent Gynecomastia and a Contemporary Literature Review. [PDF]

Epidemiologia (Basel)
Arnautu AM, Paun DL, Neamtu C, Gingu C, Nimigean V, Tilici DM, Costinescu R, Costea M, Onofrei A, Grecu B, Nacea-Radu C, Paun S.   +11 more
europepmc   +1 more source

Graded Electrolyte Disturbances Across the Spectrum of Autonomous Cortisol Secretion in Patients with Adrenal Incidentaloma: A Retrospective Cohort Study. [PDF]

J Clin Med
Li Y, Yao X, Zhao X, Zhang Y.
europepmc   +1 more source

Systemic management of adrenal malignancies: adrenocortical carcinoma and pheochromocytoma/paraganglioma. [PDF]

Endocr Connect
Hernandez-Felix JH, Lagana M, Cosentini D, Tacchetti MC, Berruti A, Del Rivero J.   +5 more
europepmc   +1 more source

Diagnosis and grading of adrenal cortical carcinoma. [PDF]

Virchows Arch
Vocino Trucco G, Duregon E, Papotti M, Volante M.   +3 more
europepmc   +1 more source

Clinical and Outcome Characteristics of Children With Adrenocortical Tumors: A Report From the International Pediatric Adrenocortical Tumor Registry

Journal of Clinical Oncology, 2004
Purpose We created a registry for pediatric adrenocortical tumors (ACTs), which are rare and are not well characterized. We provide a descriptive analysis of 254 patients registered on the International Pediatric Adrenocortical Tumor Registry. Patients and Methods Between January 1990 and December 2001, 254 patients younger than 20 years of age with ...
Bonald C Figueiredo, R Sandrini, J Jenkins   +2 more
exaly   +4 more sources

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The International Pediatric Adrenocortical Tumor Registry initiative: Contributions to clinical, biological, and treatment advances in pediatric adrenocortical tumors

Molecular and Cellular Endocrinology, 2012
Adrenocortical tumor (ACT), a rare tumor with a heterogeneous presentation, incompletely understood pathogenesis, and generally poor prognosis, occurs in 1-2 people per million and is even more uncommon in the pediatric population. Such rare cancers are a challenge to clinical practice.
Emilia Modolo Pinto, Gerard P Zambetti, Carlos Rodriguez-Galindo   +2 more
exaly   +3 more sources