Results 101 to 110 of about 1,312,119 (283)

Estado actual de las metástasis óseas [PDF]

, 2014
Los tumores óseos primarios representan solo un pequeño porcentaje comparado con las metás - tasis óseas. Pero, mientras que los tratamientos neo-adyuvantes y las técnicas de reconstrucción han mejorado la supervivencia y la calidad de vida de los ...
Amaya Valero, J.V., Angulo Sánchez, Manuel Ángel, Baeza Oliete, J., Baixauli García, Francisco, Fernández Sabaté, E., Mut Oltra, T.   +5 more
core  

Effectiveness of Gel‐immersion Endoscopic Injection Sclerotherapy Under Texture and Color Enhancement Imaging for Esophageal Varices: A Comparison of Variceal Visibility Under Gel With White Light Imaging

DEN Open, Volume 6, Issue 1, April 2026.
ABSTRACT Objective Gel‐immersion endoscopic injection sclerotherapy (GI‐EIS) addresses the technical challenges in intravariceal injection for esophageal varices (EVs). However, gel accumulation may obscure the variceal morphology. Thus, we developed GI‐EIS under texture and color enhancement imaging (TXI) and evaluated its effectiveness.
Tsunetaka Kato, Takuto Hikichi, Jun Nakamura, Minami Hashimoto, Takumi Yanagita, Mitsuru Otsuka, Daiki Nemoto, Rei Suzuki, Mitsuru Sugimoto, Hiroyuki Asama, Kentaro Sato, Hiroshi Shimizu, Kento Osawa, Rei Ohira, Masao Kobayakawa, Hiromasa Ohira   +15 more
wiley   +1 more source

Tumores renales pediátricos

Oncología, 2022
En niños menores de un año que presenten masa abdominal es lógico pensar que es de origen renal. Si bien el nefroma mesoblástico es la más común causa de tumor sólido renal en el período neonatal, no es menos cierto que, el tumor de Wilms se alza con el
Mario Veloz G., Elfa Haro H., Luis Guerrero V., Edgar Espinoza E., Juan C. Palomino P.   +4 more
doaj  

Fibropapilomatosis oral múltiple como manifestación inicial de Síndrome de Cowden: caso clínico [PDF]

, 2006
El síndrome de Cowden es una infrecuente enfermedad hereditaria englobada dentro de las poliposis gastrointestinales de tipo hamartomatoso. Se caracteriza por asociar anomalías cutaneomucosas y por la extraordinaria tendencia a desarrollar neoplasias ...
Capitán Cañadas, L.M., Durán Moreno, David, Labrot Moleón, I.L., Martínez Castillo, S.L., Salinas Sánchez, J.   +4 more
core   +1 more source

Renal Neoplasia in Cowden Syndrome [PDF]

Mayo Clinic Proceedings, 2020
Sounak, Gupta, Lori A, Erickson
openaire   +2 more sources

Incidence patterns and temporal trends of childhood cancer in Germany, 1980–2019: Forty years of childhood cancer registration in Germany

International Journal of Cancer, Volume 158, Issue 6, Page 1541-1554, 15 March 2026.
What's new? Childhood cancer ranks among the leading causes of disease‐related deaths in children in high‐income countries. Established risk factors, however, account for only a small proportion of incident childhood cancers. In this report, the authors present the first long‐term assessment of temporal trends in childhood cancer incidence rates in ...
Friederike Erdmann, Maike Wellbrock, Claudia Trübenbach, Desiree Grabow, Martin Schrappe, Peter Kaatsch, Claudia Spix, Joachim Schüz, Cécile M. Ronckers   +8 more
wiley   +1 more source

Tumor metastásico en tejido blando a nivel del sacro secundario a carcinoma de células claras de riñón. Reporte de caso

Revista Colombiana de Cirugía
Introducción. El cáncer de riñón es la undécima neoplasia maligna más común en los Estados Unidos Mexicanos. El carcinoma de células claras de riñón (CCR) es considerado la estirpe más frecuente y representa el 2-3 % de todos los cánceres a nivel ...
Ricardo O’Farril-Anzures, Martha Leticia Llamas-Ceras, Ricardo Alberto Pulido-López, Jorge Adrián Romero-Sánchez   +3 more
doaj   +1 more source

Meningioma con diferenciación rabdoide. Reporte de un caso y revisión de la bibliografía [PDF]

, 2010
Introducción: El meningioma constituye 1 a 4% de las neoplasias primarias malignas del SNC en la edad pediátrica y su incidencia se incrementa conforme a la edad.
Alvarado Bernal, Yuridia Lizeth, Ancer Rodríguez, Jesús, Barboza Quintana, Oralia, Larralde Contreras, Ligia, Miranda Maldonado, Ivett C.   +4 more
core  

Non‐RASopathy Genetic Syndromes Identified as the Molecular Cause of Disease in Patients Previously Diagnosed With Noonan Syndrome

American Journal of Medical Genetics Part A, Volume 200, Issue 3, Page 661-672, March 2026.
ABSTRACT Noonan Syndrome (NS) is a clinically and genetically heterogeneous condition characterized by typical facial dysmorphisms, short stature, congenital heart defects, and developmental delays. While variants in genes such as PTPN11, SOS1, and RAF1 account for most genetically confirmed cases, diagnosis is challenging due to phenotypic overlap ...
Gabriela Jeesoo Kim, Alexsandra Christianne Malaquias, Debora Romeo Bertola, Raissa Carneiro Rezende, Laurana De Polli Cellin, Lucas Vieira Lacerda Pires, Ana Maria Santillan‐Vasconez, Antônio Marcondes Lerario, Renata da Cunha Scalco, Alexander Augusto de Lima Jorge   +9 more
wiley   +1 more source

Segmental Tracheal Resection for Thyroid Cancer: Perioperative Morbidity, Locoregional Control, and Survival

Head &Neck, Volume 48, Issue 3, Page 644-649, March 2026.
ABSTRACT Background Segmental tracheal resection is rarely needed for advanced thyroid cancer but is among the most complex, high‐risk thyroid surgeries. Methods Retrospective study of patients undergoing segmental tracheal resection for thyroid cancer at MD Anderson Cancer Center (2005–2024).
Anastasios Maniakas, David C. Wilde, Isabelle Fournier, Emily K. Hyde, Li Xu, Jennifer R. Wang, Neil D. Gross, Erich M. Sturgis, Victoria Banuchi, Naifa L. Busaidy, Maria E. Cabanillas, Priyanka Iyer, Ramona Dadu, Steven G. Waguespack, Mimi I. Hu, G. Brandon Gunn, Michael Kwon, Salmaan Ahmed, Michelle D. Williams, Mark E. Zafereo   +19 more
wiley   +1 more source