Results 51 to 60 of about 3,934 (208)

Opsoclonus mioclonus en lactante debido a ganglioneuroblastoma: reporte de caso y revisión de literatura

Acta Neurológica Colombiana, 2019
El síndrome de Opsoclonus mioclonus ataxia (SOMA) es una entidad infrecuente en niños, caracterizada por Opsoclonus, mioclonías / ataxia y alteraciones de conducta o de sueño.
John Jairo Silvestre Avendaño, Jose Ricardo Muñoz Zúñiga, Stefania Cruz Calderón, Daniel Eduardo Morales Vásquez   +3 more
doaj   +1 more source

Neuroblastoma in Infants: Long‐Term Survival From INES Protocols A SIOPEN Study

Pediatric Blood &Cancer, Volume 72, Issue 11, November 2025.
ABSTRACT Objectives Neuroblastoma is the most common extracranial solid tumor in infants, with a possibility of spontaneous regression even in disseminated disease. Despite an overall good prognosis, relapse can worsen the outcome for some patients. A long‐term analysis is crucial to identify subgroups of patients with poorer prognosis, assessing the ...
Julie Savagner, Caroline Munzer, Gudrun Schleiermacher, Alberto Garaventa, Riccardo Haupt, Stefania Sorrentino, Katia Mazzocco, Andrea Di Cataldo, Adela Canete, Vanessa Segura, Desiree Ramal, Kate Wheeler, Ruth Ladenstein, Ana Forjaz de Lacerda, Benedicte Brichard, Maja Beck‐Popovic, Dominique Valteau‐Couanet, Claudia Pasqualini, Carole Coze, Benoit Dumont, Anne Sophie Defachelles, Marion Gambart   +21 more
wiley   +1 more source

Retroperitoneal ganglioneuroblastoma presenting as chronic diarrhea and refractory hypokalemia in a child

Indian Journal of Medical and Paediatric Oncology, 2019
Neuroblastoma is the most common extracranial solid tumor in children. Neuroblastoma presenting with diarrhea as the predominant symptom is rare and can be a diagnostic challenge to the paediatrician.
Venkateswari Ramesh, Janani Sankar, Geetha Jayapathy, Mahitha Velusamy   +3 more
doaj   +1 more source

Primary orbital ganglioneuroblastoma: A case report

Open Medicine, 2021
Ganglioneuroblastoma (GNB) is a neoplasm that arises from the primitive cells of the sympathetic nervous system during childhood. The current case is very unique because of the initial primary tumor manifestation in the orbit and an adrenal tumor being ...
Ma Ruixin, Wang Yujiao, He Weimin
doaj   +1 more source

Atypical Neuroblastoma With Absent Urinary Catecholamine Excretion and 123ImIBG Avidity Are of Favorable Outcome: A Retrospective French Single‐Center Study

Pediatric Blood &Cancer, Volume 72, Issue 11, November 2025.
Abstract Background In neuroblastoma (NB), urinary catecholamine excretion and 123ImIBG avidity—depending on tumor enzymatic activity and norepinephrine transporter expression, respectively—are diagnostic standards. The prognostic impact of atypical NB, without urinary catecholamine excretion and/or 123ImIBG avidity, remains to be determined. We sought
Anna Borovkov, Juliette Assy, Isabelle Aerts, Franck Bourdeaut, Camille Cordero, Valérie Laurence, Amaury Leruste, Sarah Winter, Jean Michon, Daniel Orbach, Hélène Pacquement, Pascale Philippe‐Chomette, Gaelle Pierron, Julien Masliah‐Planchon, Sylvie Helfre, Isabelle Janoueix‐Lerosey, Anne‐Sophie Defachelles, Claudia Pasqualini, Nina Jehanno, Joanna Cyrta, Arnaud Gauthier, Véronique Mosseri, François Doz, Sabine Sarnacki, Liesbeth Cardoen, Hervé J. Brisse, Marie Luporsi, Gudrun Schleiermacher   +27 more
wiley   +1 more source

Perioperative approach of thoracic ganglioneuroblastoma [PDF]

Revista Chilena de Anestesia, 2023
María José Andrade López, Isabella Garavis, Andrea Casanova, Diana Sarmiento, Lizeth Castro   +4 more
doaj   +1 more source

Evaluation of adrenal tumors by magnetic resonance imaging with histological correlation [PDF]

, 2008
A ressonância magnética é ferramenta importante para a detecção e caracterização dos tumores adrenais. O conhecimento das diferentes apresentações dos tumores primários e secundários à ressonância magnética e sua correlação com dados da histologia são ...
BARONI, Ronaldo Hueb, BEZERRA, Regis Otaviano Franca, BLASBALG, Roberto, CERRI, Giovanni Guido, DONATO JR., Francisco, LEITE, Claudia da Costa, LUCON, Antonio Marmo, MARTINS, Daniel Lahan, MATTEDI, Romulo Loss, VIANA, Públio Cesar Cavalcanti   +9 more
core   +2 more sources

Novel Findings in Pediatric and Adolescent Patients With Cancer and a Germline SMARCA4 Variant

Pediatric Blood &Cancer, Volume 72, Issue 9, September 2025.
ABSTRACT Introduction SMARCA4 is a known susceptibility gene for malignant rhabdoid tumors (MRT) in children and small cell carcinoma of the ovary hypercalcemic type (SCCOHT) in young females and women. Recently, a novel association between germline SMARCA4 variants and predisposition to neuroblastoma was proposed.
Nienke van Engelen, Ronald. R. de Krijger, Michelle M. Kleisman, Lennart. A. Kester, Saskia M. J. Hopman, Mariette E. G. Kranendonk, Marijn A. Vermeulen, Carli Tops, Seok‐Young Kim, Hans Clevers, Kornelia Neveling, Roland. P. Kuiper, Marjolijn C. J. Jongmans   +12 more
wiley   +1 more source

Trends of surgical treatment and enhanced recovery after surgery (ERAS) application for adrenal tumors: An 11‐year observational study based on electronic medical record

UroPrecision, Volume 3, Issue 3, Page 153-160, September 2025.
Abstract Background Adrenal tumor is a common condition that often requires adrenalectomy. The objective of this study is to compare the safety and implementation of the enhanced recovery after surgery (ERAS) among patients who received open, laparoscopic and robotic‐assisted operation.
Bingfeng Luo, Chi Yao, Yongle Zhan, Yuan Yuan, Sucai Liao, Zhenquan Lu, Rong Na, Richard K. Lo   +7 more
wiley   +1 more source

Ganglioneuroblastoma of the Thoracic Spinal Cord: a Very Rare Case Report

Acta Medica, 2012
An eight‑month‑old male child was admitted with weakness and swelling in the feet. Paraparesis and bilateral lower extremity edema were present in the neurological examination.
Bekir Akgun, Deniz Ates, Metin Kaplan
doaj   +1 more source