Results 101 to 110 of about 29,255 (243)
Rare case of primary bladder Wilm's tumor in a 1-year old boy
Urology Case Reports, 2019 Extrarenal Wilms' tumor (EWRT) is a rare entity, but primary bladder Wilm's tumor is even rarer with only 1 case reported. A 1-year old boy came with chronic urinary retention.
Jufriady Ismy +3 more
doaj +1 more source
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 +9 more
wiley +1 more source
Quantitative RT-PCR-based miRNA profiling of blastemal Wilms’ tumors
, 2018 A blastemás Wilms-tumorok kedvezőtlen prognózist mutatnak a kemoterápiára való alacsony érzékenység miatt. Célunk a kísérlet során az volt, hogy hozzájáruljunk a betegség miRNSprofilozásához és megvizsgáljuk, hogy felhasználhatunk-e FFPE mintákat miRNS-
Berki, Zsanett
core
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 +17 more
wiley +1 more source
Rhabdomyosarcoma mimicking Wilms' tumor
, 1994 A case of a 6 year old child, with a pleomorphic rhabdomyosarcoma involving simultaneously the leg muscles and the kidney is reported. The renal tumor distorted the pyelocalycial system and Wilms' tumor was the clinical diagnosis.
Mendonça, Núbia [UNESP] +2 more
core +1 more source
JA Clinical Reports, 2020 Background Wilms’ tumor with hyperreninemia may result in critical cardiovascular decompensation. We report a case of severe hypertensive heart failure followed by tumor resection in a 3-month-old infant with Wilms’ tumor. Case presentation A 3-month-old
Hiroko Miura +4 more
doaj +1 more source
Pediatric Blood &Cancer, Volume 73, Issue 6, June 2026.ABSTRACT Purpose Malignant rhabdoid tumor of the kidney (MRTK) is a rare, aggressive tumor seen in young children. The optimal timing of resection for locally advanced tumors is not well‐defined. The purpose of this study is to evaluate modern oncologic outcomes and the impact of surgical timing. Methods A multicenter retrospective review was performed
Hannah N. Rinehardt +76 more
wiley +1 more source
Clinical Case Reports, Volume 14, Issue 6, June 2026.ABSTRACT Malignant small round cell tumors are a heterogeneous group of aggressive neoplasms characterized by small, round cell morphology. The undifferentiated cells in these tumors exhibit a high nuclear‐cytoplasmic ratio, and definitive histologic diagnosis via light microscopy can be extremely challenging. Diagnostic accuracy significantly improves
George Evele +3 more
wiley +1 more source
Horseshoe kidney with teratoid type of Wilms tumor: a rare case report
BMC NephrologyBackground Horseshoe kidney is the most common renal fusion anomaly, and Wilms tumor is the most frequent renal malignancy in children. The occurrence of Wilms tumor in association with horseshoe kidney is a scarce anomaly.
Nafiseh Mortazavi +6 more
doaj +1 more source
Adult Wilms' tumor with calcification untreated for 5 years – a case report
BMC Urology, 2004 Background Wilms' tumor is rarely found in adults and there are no established treatment guidelines for such tumors in adults. Whereas calcification is a common finding in neuroblastoma, it is considered uncommon in Wilms' tumor.
Nakajima Fumitaka +4 more
doaj +1 more source