Results 31 to 40 of about 2,093 (107)
Bilateral Gonadoblastoma in a 12‐Year‐Old Girl 4 Years After Wilms' Tumor: A Rare Pediatric Case
ABSTRACT This case of a 12‐year‐old patient who developed bilateral gonadoblastoma 4 years after treatment for Wilms tumor highlights the importance of rigorous, risk‐adapted long‐term surveillance and careful evaluation of incidental gonadal findings, even in asymptomatic patients.
Ahmed Quraish +4 more
wiley +1 more source
Esfínter Urinario Artificial AMS 800” colocados en pacientes con incontinencia urinario luego de prostatectomía radical. El Dr. Alejandro Manduley de Panamá, nos presenta su experiencia en la “Incorporación de la perfusión dinámica” en programa ...
Carlos Francisco Figueroa Lemus +1 more
doaj
ABSTRACT Chemotherapy‐induced peripheral neuropathy remains a major complication in pediatric cancer, with disrupted somatosensory and nociceptive processing being a key aspect. This review synthesizes empirical studies on alterations in somatosensory and nociceptive processing in children and adolescents with cancer.
Julia Schweiger +4 more
wiley +1 more source
Aggressive Desmoplastic Small Round Cell Tumor in an Adult: A Case Report and Literature Review
ABSTRACT Desmoplastic small round cell tumor (DSRCT) is a rare and highly aggressive sarcoma that predominantly affects adolescents and young adults. It is defined by a characteristic chromosomal translocation, t(11;22) (p13;q12), resulting in the EWS–WT1 fusion gene.
Seyed Amir Aledavood +4 more
wiley +1 more source
Abstract Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke‐like episodes (MELAS) is a rare multisystem mitochondrial disorder primarily caused by mutations in mitochondrial DNA. While it typically presents with stroke‐like episodes, seizures, and lactic acidosis, recent evidence highlights a broader clinical spectrum, including ...
Faezeh Khorshidian +3 more
wiley +1 more source
Congenital aniridia: European COST action ANIRIDIA‐NET guidelines for diagnosis, management and care
Abstract Congenital aniridia is a rare ocular disorder affecting the majority of eye structures and can be associated with systemic manifestations. The main visible phenotypic characteristic is the partial or complete absence of the iris; however, foveal hypoplasia is a more frequent and reliable clinical sign. Other ocular comorbidities are associated
Davide Romano +26 more
wiley +1 more source
Bilateral Wilms Tumor: Looking for the Best Surgical Strategy. [PDF]
Martos Rodríguez M +19 more
europepmc +1 more source
Kidney transplantation outcomes in children with WT1-associated kidney disease: a single-center cohort study. [PDF]
Abasi R +5 more
europepmc +1 more source

