نتایج جستجو برای: adrenocortical adenoma

تعداد نتایج: 27212  

Journal: :Annals of nuclear medicine 1999
I J Ochotorena H Miyake Y Hori H Odo Y Hirata H Mori

Extraadrenal abnormal uptake on adrenocortical scintigraphy has been reported rarely in the normal gallbladder, lipid cell tumor of the ovary, or in clear cell type renal cell carcinoma. Clear cell type renal cell carcinoma contains glycogen and cholesterol like the adrenal gland, but the uptake of the radionuclide I-131 cholesterol has been reported to be low and not sufficient to image it. Ri...

A RABBANI, J AHMADI, M MOSAVATI, M RAZZAGHIAZAR, N NEZAKATGOO, Y SHAFEGHATY,

During a period of IS years from 1975 to 1989, eleven children with adrenocortical tumors were managed with relatively favorable results in our center. Despite its rarity in the pediatric age group, our series is one of the largest reported in the literature in the given period of time. All of our 11 patients presented with hyperfunction of the adrenal cortex. Virilization alone was the mo...

Journal: :Annals of the Academy of Medicine, Singapore 2006
Ling Choo Lim Leonard H C Tan C Rajasoorya

INTRODUCTION We present a rare variety of adrenocorticotrophic hormone (ACTH)-independent Cushing's syndrome known as primary pigmented nodular adrenocortical disease (PPNAD). CLINICAL PICTURE The patient initially underwent unilateral adrenalectomy for what was thought to be a left adrenal adenoma. OUTCOME Partial resolution of symptoms and demonstrable persistent hypercortisolism after su...

Journal: :BMJ case reports 2017
Fady Hannah-Shmouni Georgios Z Papadakis Constantine A Stratakis Jenny Blau

Hannah-Shmouni F, et al. BMJ Case Rep 2017. doi:10.1136/bcr-2017-220820 Description A 70-year-old woman with controlled type 2 diabetes mellitus and hypertension presented for evaluation of chronic abdominal discomfort. An incidental 3.2×3.5×3 cm left adrenal mass was identified on CT. Physical examination revealed obesity stage 2 without a Cushingoid appearance and controlled hypertension with...

Journal: :medical journal of islamic republic of iran 0
m razzaghiazar from the department of pediatric surgery and pediatric endocrinology, children's medical center hospital.tehran university of medical sciences j ahmadi from the department of pediatric surgery and pediatric endocrinology, children's medical center hospital. tehran university of medical sciences a rabbani from the department of pediatric surgery and pediatric endocrinology, children's medical center hospital. tehran university of medical sciences n nezakatgoo from the department of pediatric surgery and pediatric endocrinology, children's medical center hospital. tehran university of medical sciences m mosavati from the department of pediatric surgery and pediatric endocrinology, children's medical center hospital. tehran university of medical sciences y shafeghaty shahid rahnamoon hospital, iran university of medical sciences, tehran, islamic republic of lran.

during a period of is years from 1975 to 1989, eleven children with adrenocortical tumors were managed with relatively favorable results in our center. despite its rarity in the pediatric age group, our series is one of the largest reported in the literature in the given period of time. all of our 11 patients presented with hyperfunction of the adrenal cortex. virilization alone was the most fr...

2015
Helene Myrtue Nielsen Alexandre How-Kit Carole Guerin Frederic Castinetti Hans Kristian Moen Vollan Catherine De Micco Antoine Daunay David Taieb Peter Van Loo Celine Besse Vessela N Kristensen Lise Lotte Hansen Anne Barlier Frederic Sebag Jörg Tost

Overexpression of insulin growth factor 2 (IGF2) is a hallmark of adrenocortical carcinomas and pheochromocytomas. Previous studies investigating the IGF2/H19 locus have mainly focused on a single molecular level such as genomic alterations or altered DNA methylation levels and the causal changes underlying IGF2 overexpression are still not fully established. In the current study, we analyzed 6...

Journal: :Hormones 2011
Kerstin Hagemann Maura Zanolari Calderari Aurel Perren Ian Cree Primus E Mullis Christa E Flück

UNLABELLED Adrenocortical tumors are rare in children and present with variable signs depending on the type of hormone excess. We herein describe the unusual presentation of a child with adrenocortical tumor and introduce the concept of in vitro chemosensitivity testing. CASE REPORT A 10.5-year-old girl presented with hypertrichosis/hirsutism and weight loss. The weight loss and behavioral pr...

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