Results 101 to 110 of about 29,311 (229)

Outcomes and Surgical Management of Malignant Rhabdoid Tumor of the Kidney: A Report From the Pediatric Surgical Oncology Research Collaborative

open access: yesPediatric 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

Pedunculated and obstructive Wilms' tumor: A rare presentation in a 2 year-old male

open access: yesUrology Case Reports, 2018
Wilms' tumor manifesting as an obstructing ureteral mass is extremely rare. Herein, we report an unusual case in which a child presented with a clinical picture concerning for and suggestive of ureteropelvic junction obstruction (UPJO), but was instead ...
Leor T. Arbel   +2 more
doaj   +1 more source

Organ‐Specific and Conserved Regulatory Logic Orchestrates Gene Expression in the Embryonic Mesothelium

open access: yesAdvanced Science, Volume 13, Issue 34, 19 June 2026.
Integrated multi‐omic profiling maps the gene‐regulatory landscape of the coelomic mesothelium across heart, lung, and pancreas. A cardiac‐restricted regulatory program is uncovered in which TBX20 activates heart mesothelial (epicardial) cis‐regulatory elements, while MAF emerges as a conserved regulator of mesothelial identity.
Quang Minh Dang   +3 more
wiley   +1 more source

An Atypical Presentation, Diagnostic Challenges, and Treatment Response of a Malignant Small Round Cell Tumor in the Lumbo‐Inguinal Region of an Infant

open access: yesClinical 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

The Clinical Relevance of Age at Presentation in Nephroblastoma

open access: yes, 2016
The most important prognostic factors for Wilms tumor (WT) patients seem to be stage, histological subtype, and 1p/16q loss of heterozygosity (LOH) in chemotherapy-naive WTs.

core   +1 more source

Wilms’ Tumor: Histopathological Variants and the Outcomes of 31 Cases at a Tertiary Care Center in Northern India

open access: yesMiddle East Journal of Cancer, 2017
Background: Wilms’ tumor is the most common malignant renal tumor in the pediatric age group. This tumor is classically managed by multimodal treatment which involves surgery, radiotherapy and chemotherapy.
Kamal Nain Rattan   +2 more
doaj  

WILMS' TUMOR [PDF]

open access: yesAmerican Journal of Roentgenology, 1968
W C, Black, E F, Ragsdale
openaire   +2 more sources

Methyltransferase‐Like 14 Promotes the Angiogenesis of Hepatocellular Carcinoma via Targeting Vascular Endothelial Growth Factor A

open access: yesCancer Reports, Volume 9, Issue 6, June 2026.
ABSTRACT Background N6‐methyladenosine (m6A) modification is a pivotal epitranscriptomic regulator implicated in tumor progression. As a core component of the m6A methyltransferase complex, METTL14 is known to suppress tumorigenesis; however, its specific role in tumor angiogenesis remains elusive. Given that Vascular Endothelial Growth Factor A (VEGFA)
Xinmiao Xiong   +5 more
wiley   +1 more source

External Beam Radiation Therapy for Wilms Tumor

open access: yes, 2022
This project explains Wilms tumor cancer and the role radiation therapy can play in treating patients who have the disease. General statistics, symptoms, cancer severity, contributing factors, imaging options, and treatment options are also discussed ...
Galdi, Alyssa
core  

Wilms' Tumor [PDF]

open access: yesCA: A Cancer Journal for Clinicians, 1981
J, Belasco, G J, D'Angio
openaire   +2 more sources

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