Results 11 to 20 of about 6,153 (148)

Adrenocortical carcinoma: Pediatric aspects (Review)

Experimental and Therapeutic Medicine, 2022
Adrenocortical carcinoma (adrenal cortex-derived cancer), an orphan malignancy, is a very aggressive disease that affects both adults and children with an annual incidence of 1-2 adult and 0.2-0.38 pediatric cases/million (in the pediatric population it represents 0.2% of all cancers), with a female predominance.
Florica, Sandru, Răzvan-Cosmin, Petca, Mara, Carsote, Aida, Petca, Mihai Cristian, Dumitrascu, Adina, Ghemigian   +5 more
openaire   +3 more sources

DAX-1 Expression in Pediatric Rhabdomyosarcomas: Another Immunohistochemical Marker Useful in the Diagnosis of Translocation Positive Alveolar Rhabdomyosarcoma [PDF]

, 2015
OBJECTIVES: The aim of this study was to investigate the expression of DAX-1 in a series of pediatric rhabdomyosarcomas (RMS) with known translocation and compare it to Ap2\u3b2, known to be selectively expressed in ARMS. DESIGN: We revised a series of
Alaggio, Rita, Bisogno, Gianni, Cecchetto, Giovanni, Dall'Igna, Patrizia, Lalli, Enzo, Lazzari, Elena, Poli, Elena, Roma, Josep, Universitat Autònoma de Barcelona, Virgone, Calogero, Zin, Angelica   +10 more
core   +20 more sources

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

Pediatric Adrenocortical Carcinoma Presenting With Virilization: A Case of a Low-Grade Tumor in a Young Child. [PDF]

Cureus
Askar A, Mohamed SF, Hussein Al-Mutair M.   +2 more
europepmc   +2 more sources

Adrenocortical carcinoma in a pediatric patient with li-fraumeni-like Syndrome: an endemic condition in southern Brazil [PDF]

Clinical & Biomedical Research, 2021
A 12-year-old boy with germline TP53-R337H mutation and family history of early adrenocortical carcinoma (ACC) was admitted to hospital with abdominal pain and distention. During the physical examination he presented cushingoid facies, high blood pressure and pulse rate.
Mendes Knabben, Mariana, Reis Caldas, Renan, Onofre de Brito Lima, Jéssica, Spader Casagrande, Aline, Lorenzoni Almeida Ghezzi, Caroline   +4 more
openaire   +4 more sources

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

Pediatric adrenocortical carcinoma revealed by isolated Cushing syndrome: A case report

Journal of Pediatric Surgery Case Reports, 2023
Background: Adrenocortical carcinoma accounts for less than 0.2% of all pediatric malignancies. Virilization is the most common revealing sign, whereas hyperaldosteronism and Cushing syndrome are less common.We report a case of adrenocortical carcinoma which was revealed by Cushing syndrome and successfully treated in an adolescent girl.
Hakima Chafaaoui, Assan Beaudelaire Romulus, Saad Andaloussi, Omar Dalero, Aziz Elmadi   +4 more
openaire   +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

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

Bilateral Adrenal Mass Secondary to Bilateral Infantile Neuroblastoma in an Infant With Beckwith-Wiedemann Syndrome. [PDF]

Clin Case Rep
ABSTRACT Infants with Beckwith‐Wiedemann syndrome face a high risk of embryonal tumors, necessitating early and consistent surveillance. This case illustrates how timely imaging and biochemical monitoring enabled successful non‐surgical management of bilateral adrenal neuroblastoma.
Nigusie M, Arega G, Hailu A, Kassahun A, Fikad G, Chalachew T, Balta B.   +6 more
europepmc   +2 more sources