Results 41 to 50 of about 19,884 (196)

Virilizing adrenocortical carcinoma in a child: A rare enigma

Indian Journal of Endocrinology and Metabolism, 2012
Adrenocortical carcinomas are rare tumors with an incidence of one to two cases per million population and are still more rarer in the pediatric age group.
Varuna Sipayya, Yogesh K Yadav, Rashmi Arora, Uma Sharma, Kusum Gupta   +4 more
doaj   +1 more source

Long-term survival outcomes of pediatric adrenal malignancies: An analysis with the upstaged SEER registry during 2000-2019

Frontiers in Endocrinology, 2022
ObjectiveTo investigate the clinicopathological characteristics and long-term survival outcomes of pediatric adrenal malignancies.MethodThis study retrospectively analyzed children with pathologically confirmed pediatric adrenal malignancies from ...
Zemin Lv, Yunyun Yu, Yangmei Luo, Song Lin, Xuang Xiang, Xiaowen Mao, Shigang Cheng   +6 more
doaj   +1 more source

Mature Cystic Teratoma of the Right Adrenal Gland in a Pediatric Patient: A Case Report. [PDF]

Clin Case Rep
ABSTRACT Adrenal teratomas are rare neoplasms, most often benign but with potential for malignant transformation, particularly in the pediatric population. A seven‐year‐old girl from kawasoti, Nepal, presented with intermittent right‐sided abdominal pain for 2 months, initially attributed to dietary factors such as junk food intake.
Gautam A, Adhikari P, Bhandari S, Miya JA, Tiwari N.   +4 more
europepmc   +2 more sources

New directions for the treatment of adrenal insufficiency [PDF]

, 2015
The following funding bodies supported this work: Biotechnology and Biological Sciences Research Council (BBSRC BB/L00267/1, to LG), Rosetrees Trust (to LG), Barts and The London Charity (417/2235, to LG), EU COFUND (PCOFUND-GA-2013-608765, to LG and GRB)
Allen, Allende, Badylak, Bancos, Berkes, Birke, Buaas, Chamoux, Chamoux, Clipsham, Cogger, Cox, Crawford, Drucker, Dubernard, El-Khairi, Else, Faulk, Fayard, Franksson, Freedman, Gallo-Payet, Gondo, Gondo, Grodstein, Guasti, Guasti, Hardy, Hardy, Hardy, Hardy, Hatano, Huang, Huang, Ibbertson, Jadhav, Kearns, Kim, King, Laufer, Ludwig, Luo, Mazilu, Parker, Sancho-Martinez, Schimmer, Schnabel, Sonoyama, Takahashi, Tanaka, Teebken, Thomas, Thomas, Thomas, Thomas, Thomas, Val, Val, Vierbuchen, Vouillarmet, Walczak, Walczak, Wei, Wilhelm, Wong, Yazawa, Yazawa, Yazawa, Yazawa, Zupekan   +69 more
core   +2 more sources

GLUT1 expression in pediatric adrenocortical tumors: a promising candidate to predict clinical behavior [PDF]

, 2017
Background: Discrimination between benign and malignant tumors is a challenging process in pediatric adrenocortical tumors. New insights in the metabolic profile of pediatric adrenocortical tumors may contribute to this distinction, predict prognosis, as
Allolio, Allolio, Allolio, Almeida, Arap, Baltazar, Baltazar, Baltazar, Baltazar, Baltazar, Baudin, Bouley, Casal, Casal, Chatterjee, Chuang, Deal, DeLacerda, Fassnacht, Felix, Figueiredo, Figueiredo, Gatenby, Gillies, Gottlieb, Gow, Hammer, Heffess, Hellerbrand, Jiang, Kavan, Kebebew, Kjellman, Kuhajda, Lacroix, Latronico, Latronico, Liang, Mak, Mendonca, Moir, Nadel, Namer, Pereira, Pouyssegur, Ribeiro, Sambuceti, Sandrini, Sun, Tabarin, Tissier, Tracy, Vander Heiden, Wajapeyee, Weinberg, Weiss, Weldon, Wieand, Yunes, Zambetti, Zerbini   +60 more
core   +2 more sources

Retroperitoneoscopic adrenalectomy in an infant with adrenocortical virilizing tumor

São Paulo Medical Journal, 2002
CONTEXT: Adrenocortical virilizing tumors are rare in the pediatric age group. Laparoscopic surgery is the gold standard method for treatment of adrenal functional tumors under 6 cm in size, in adults.
Marcos Tobias-Machado, Jairo Cartum, Telma Murias Santos-Machado, Heloísa Amaral Gaspar, Alexandre Sibanto Simões, Ricardo Cruz, Renata Rodrigues, Roberto Vaz Juliano, Eric Roger Wroclawski   +8 more
doaj   +1 more source

Outcome after resection of Adrenocortical Carcinoma liver metastases: a retrospective study [PDF]

, 2017
Background: Metastatic Adrenocortical Carcinoma (ACC) is a rare malignancy with a poor 5-year-survival rate (
Christine Spitzweg, Christoph-Thomas Germer, Felix Megerle, Johannes Baur, Marcus Quinkler, Martin Fassnacht, Matthias Kroiss, on behalf of the German Adrenocortical Carcinoma Study Group, Peter Nawroth, Timo Deutschbein, Tjark-Ole Büntemeyer, Ulrich Steger   +11 more
core   +1 more source

Li-Fraumeni syndrome: Adrenal cortical tumor in a newborn followed by a choroid plexus tumor

Journal of Pediatric Surgery Case Reports, 2018
Adrenocortical tumors (ACTs) are rare in children, comprising
Jamie E. Anderson, Rebecca A. Stark
doaj   +1 more source

Adrenocortical tumors in children: Sri Lankan experience from a single center, and a mini review

Journal of Medical Case Reports, 2023
Background Pediatric adrenocortical tumors include both benign adenomas and highly virulent malignant tumors. However, they are very rare among children.
Naotunna Palliya Guruge Chamidri Randika Naotunna, Harankaha Vidanalage Dinendra Nishadini Siriwardana, Balagamage Chamila Lakmini, Dilhara Senani Gamage, Sandani Gunarathna, Malik Samarasinghe, Sanjeewa Gunasekara, Navoda Atapattu   +7 more
doaj   +1 more source

Effects of o,p’-DDE, a Mitotane Metabolite, in an Adrenocortical Carcinoma Cell Line

Pharmaceuticals, 2022
In South Brazil, the incidence of pediatric adrenocortical carcinoma (ACC) is higher than in other regions and countries worldwide. The ACC treatment includes therapy with mitotane, the only adrenolytic drug approved by the FDA.
Camila Bach, Claudia Rita Corso, Alan de Almeida Veiga, Mariana Martins Paraizo, Lauro Mera de Souza   +4 more
doaj   +1 more source