Results 91 to 100 of about 93,458 (289)

Glycometabolic Alterations in Secondary Adrenal Insufficiency: Does Replacement Therapy Play a Role? [PDF]

, 2018
Secondary adrenal insufficiency (SAI) is a potentially life-threatening endocrine disorder due to an impairment of corticotropin (ACTH) secretion from any process affecting the hypothalamus or pituitary gland.
Gianfrilli, Daniele, Graziadio, Chiara, Hasenmajer, Valeria, Isidori, Andrea M., Sbardella, Emilia, Venneri, Mary A.   +5 more
core   +2 more sources

Autocrine/paracrine regulatory mechanisms in adrenocortical neoplasms responsible for primary adrenal hypercorticism.

European Journal of Endocrinology, 2013
A wide variety of autocrine/paracrine bioactive signals are able to modulate corticosteroid secretion in the human adrenal gland. These regulatory factors, released in the vicinity of adrenocortical cells by diverse cell types comprising chromaffin cells,
H. Lefebvre, Gaëtan Prévost, E. Louiset   +2 more
semanticscholar   +1 more source

Evaluation of adrenal tumors and analysis of the metabolic profile of patients with incidentaloma [PDF]

Revista do Colégio Brasileiro de Cirurgiões
Introduction: Advances in imaging methods have led to an increasingly frequent diagnosis of adrenal gland lesions as incidental findings. Despite progress in this field, there is still limited information regarding the epidemiology of the clinical and ...
PEDRO VICTOR GONÇALVES MONTALVÃO, IURI MOURA MANGUEIRA, GABRIEL DA MOTTA ALVES, JOÃO VITOR FAZZIO CORDEIRO, MARCIA HELENA SOARES COSTA, GUILHERME DE ANDRADE GAGHEGGI RAVANINI   +5 more
doaj   +1 more source

Neuroendocrine Tumors (NETs) : A population-based study of incidence and survival in Girona province, 1994-2004 [PDF]

, 2012
Els tumors neuroendocrins (TNEs) són un grup de neoplàsies poc freqüents i heterogènies i amb un ampli espectre d'agressivitat. Hi ha molt poca informació epidemiològica a nivell mundial, l'objectiu d'aquest estudi ha estat el de reportar-ne les dades a ...
Alsina Maqueda, Maria, Galceran, Joan Carles, Universitat Autònoma de Barcelona. Departament de Medicina, Universitat Autònoma de Barcelona. Facultat de Medicina   +3 more
core  

Ganglioneuroma Always A Histopathological Diagnosis [PDF]

, 2011
Neuroblastoma, ganglioneuroblastoma and ganglioneuroma arise from sympathetic tissue in the neck, posterior mediastinum, adrenal gland, retroperitoneum and pelvis Ganglioneuromas are commonly seen in childhood.
K, Balaiah, S, Gnana Prakash, Shetty, Prasad K, Shetty, Prasanna K   +3 more
core   +1 more source

Aspectos clínicos e moleculares de tumor adrenocortical metacrônico pediátrico [PDF]

, 2011
The occurrence of metachronous adrenocortical carcinoma has rarely been described. We report a case of a child with virilizing adrenocortical metachronous tumors that, despite several metastases, presented long-term survival (15 years).
ALENCAR, Guilherme Asmar, ALMEIDA, Madson Queiroz, BRITO, Luciana Pinto, DOMENICE, Sorahia, FRAGOSO, Maria Candida Barrison Villares, LATRONICO, Ana Claudia, LERARIO, Antonio Marcondes, LIMA, Lorena de Oliveira, MENDONCA, Berenice Bilharinho   +8 more
core   +2 more sources

Outcomes and Follow-Up Trends in Adrenal Leiomyosarcoma: A Comprehensive Literature Review and Case Report

Journal of Clinical Medicine
Background: Leiomyosarcoma (LMS) originating from the adrenal gland is exceedingly rare, constituting a minute fraction of soft tissue sarcomas. Due to its rarity, with less than 50 documented cases in English medical literature, the diagnosis and ...
F. Mongardini, Maddalena Paolicelli, A. Catauro, Alessandra Conzo, Luigi Flagiello, G. Nesta, Rosetta Esposito, Andrea Ronchi, Alessandro Romano, R. Patrone, L. Docimo, Giovanni Conzo   +11 more
semanticscholar   +1 more source

Symptomatic ovarian steroid cell tumor not otherwise specified in a post-menopausal woman

Rare Tumors, 2016
Steroid cell tumor not otherwise specified (NOS) is a rare subtype of sex cord stromal tumor of the ovary and contributes less than 0.1% of all ovarian neoplasms.
Neha Sood, Kaniksha Desai, Ana-Maria Chindris, Jason Lewis, Tri A. Dinh   +4 more
doaj   +1 more source

Adrenal myelolipoma associated with cholelithiasis

Indian Journal of Urology, 2001
Myelolipomas are usually as ymptomatic and discovered incidentally or at autopsy. They are rare benign adrenal neoplasms, characterized by the presence of adipose tissue and elements of haematopoietic tissue in various degrees of differentiation ...
Dilip K Kar, Amit Agarwal, Anand K Mishra, Sushil K Gupta, Kaushal K Prasad, Vijay Sawlani, Lily Pal, Saroj K Mishra   +7 more
doaj  

Succinate dehydrogenase (SDH)-deficient renal carcinoma:a morphologically distinct entity: a clinicopathologic series of 36 tumors from 27 patients [PDF]

, 2014
Succinate dehydrogenase (SDH)-deficient renal carcinoma has been accepted as a provisional entity in the 2013 International Society of Urological Pathology Vancouver Classification.
Belinsky, Cascon, Cascon, Chou, Dwight, Dwight, Eng, Fairchild, Fishbein, Fleming, Gaal, Gill, Gill, Gill, Gill, Gill, Gill, Gill, Gill, Gimm, Henderson, Housley, Janeway, Jasperson, Korpershoek, Malinoc, Miettinen, Miettinen, Miettinen, Neumann, Ni, Oudijk, Paik, Papathomas, Ricketts, Ricketts, Said-Al-Naief, Schimke, Solis, Srigley, Srirangalingam, Srirangalingam, van Nederveen, van Nederveen, Vanharanta, Wagner, Xekouki   +46 more
core   +3 more sources