Results 91 to 100 of about 11,107 (213)

Wilms’ Tumor in children treated at the provincial pediatric hospital of Holguín

Revista Electrónica Dr. Zoilo E. Marinello Vidaurreta, 2020
Background: Wilms’ tumor is a malignant neoplasia whose origin has been attributed to disorders in the renal histogenesis. It has been described as the fifth malignant neoplasia in pediatrics; it is the commonest renal tumor.Objective: to describe a ...
Onelis Góngora-Gómez, Juan Pablo Carballido-Sánchez, Yadnil Elizabeth Gómez-Vázquez, Rosalí Bauta-Milord, Adrián Ramírez-Quintana   +4 more
doaj  

Evaluating the Utility of Paired Tumor and Germline Targeted DNA Sequencing for Pediatric Oncology Patients: A Single Institution Report

Pediatric Blood &Cancer, Volume 73, Issue 7, July 2026.
ABSTRACT Objective To evaluate the diagnostic yield and utility of universal paired tumor–normal multigene panel sequencing in newly diagnosed pediatric solid and central nervous system (CNS) tumor patients and to compare the detection of germline pathogenic/likely pathogenic variants (PV/LPVs) against established clinical referral criteria for cancer ...
Natalie Waligorski, Rebecca Ronsley, Shannon M. Stasi, Jeffrey Stevens, Erin R. Rudzinski, Christina M. Lockwood, Sarah E. S. Leary, Bonnie L. Cole, Michelle A. Ting, Vera Paulson   +9 more
wiley   +1 more source

Kidney transplantation in patients with Wilms' tumor. [PDF]

, 1992
We report our experience of renal transplantation in three patients treated for Wilms' tumor (with lung metastasis in two of them), and review 26 previously reported cases in order to define the current indications of transplantation in this setting. Our
Cornu, Guy, Alexandre, Guy P., Ninane, J., Van Ypersele de Strihou, Charles, Pais, E., Pirson, Yves, Squifflet, Jean-Paul   +6 more
core   +1 more source

The Fate (Outcome) of Clinically Apparent Single Lesion and Oligofocal Nephroblastomatosis Treated According to SIOP/GPOH Protocols for Wilms Tumor

Pediatric Blood &Cancer, Volume 73, Issue 7, July 2026.
ABSTRACT Background The management of clinically apparent single lesions or oligofocal nephroblastomatosis, a facultative precursor of nephroblastoma, remains debated. Methods We retrospectively analyzed 37 patients with clinically apparent single or oligofocal nephroblastomatosis (two to three lesions per kidney) among 2347 patients registered between
Nils Welter, Jens‐Peter Schenk, Jenny Wegert, Manfred Gessler, Leo Kager, Stefan Wagenpfeil, Marina Müller, Jean‐Michel Wolff, Joerg Fuchs, Steven W. Warmann, Clemens‐Magnus Meier, Jochen Hubertus, Christian Rübe, Christian Vokuhl, Patrick Melchior, Lena Tschirner, Norbert Graf, Rhoikos Furtwängler   +17 more
wiley   +1 more source

Tumor de Wilms en niños atendidos en el hospital pediátrico provincial de Holguín [PDF]

, 2020
Background: Wilms’ tumor is a malignant neoplasia whose origin has been attributed to disorders in the renal histogenesis. It has been described as the fifth malignant neoplasia in pediatrics; it is the commonest renal tumor.Objective: to describe a ...
Carballido-Sánchez, Juan Pablo, Góngora-Gómez, Onelis, Bauta-Milord, Rosalí, Gómez-Vázquez, Yadnil Elizabeth, Ramírez-Quintana, Adrián   +4 more
core  

Cavectomy for the treatment of Wilms tumor with vascular extension [PDF]

, 2006
Purpose: Vascular extension to the vena cava occurs in 4% of Wilms tumor cases and can reach the right atrium in up to 1%. When this happens the thrombus is usually not adherent to the vessel wall, and there is blood flow around it.
Fonseca, José Honório de Almeida Palma da [UNIFESP], Silva, Nasjla Saba da [UNIFESP], Ribeiro, R. C., Schettini, Sergio Tomaz [UNIFESP], Cypriano, Monica [UNIFESP], Abib, Simone de Campos Vieira [UNIFESP]   +5 more
core   +1 more source

Proposal of a Risk Stratification Algorithm for Extracranial Malignant Rhabdoid Tumors

Cancer Medicine, Volume 15, Issue 7, July 2026.
ABSTRACT Background Malignant rhabdoid tumors (MRT) are highly aggressive tumors, primarily described in children, but also affecting adults. The objective was to identify independent prognostic factors to predict individual patients' risk and to establish an age‐spanning risk stratification system for prospective trials. Patients and Methods Data from
Juno Eberl, Angelika Eggert, Monika Scheer   +2 more
wiley   +1 more source

Cisto multilocular renal

Revista do Colégio Brasileiro de Cirurgiões
O cisto multilocular renal é uma tumoração rara, de etiopatogenia discutida, que apresenta um aspecto macroscópico característico (parecendo favos de mel) mas histologia variável, o que ocasionou uma vasta sinonímia para esta afecção.
Ennio Gabriel, Wilberto Trigueiro, Dailton Medeiros, Vamberto Costa Filho, Sandra Bonfim Silva Barbosa, Alexandre Aranha Trigueiro   +5 more
doaj   +1 more source

Aniridia congénita

Repertorio de Medicina y Cirugía, 2011
Objetivo: presentar un caso de aniridia congénita bilateral asociada con catarata e hipoplasia foveal y revisar la literatura existente. Métodos: revisión de la literatura y de la historia clínica de un paciente que consultó al Hospital de San José de ...
Adriana Solano, Juan Díaz Granados, Ángela Castillo   +2 more
doaj   +1 more source

Clear Cell Sarcoma of the Kidney Case Reports Should Connect Renal‐Origin Imaging With Staging, Treatment Rationale, and Follow‐Up

Clinical Case Reports, Volume 14, Issue 7, July 2026.
ABSTRACT In pediatric clear cell sarcoma of the kidney, ultrasound and CT are valuable for identifying renal‐origin malignant features, but imaging alone does not fully communicate oncologic risk. Future case reports should connect imaging and histopathology with staging basis, nodal pathology, margin/spillage status, treatment protocol, radiotherapy ...
Muhammad Abdullah Awan, Hammad‐ud‐din Raza   +1 more
wiley   +1 more source