Results 141 to 150 of about 29,255 (243)

Distinct pathways for genetic and epigenetic predisposition in familial and bilateral Wilms tumor

Genome Medicine
Background Genetic predisposition is particularly common in children with the kidney cancer, Wilms tumor. In 10% of these children, this manifests as a family history of Wilms tumor or bilateral disease.
Jenny Wegert, Silke Appenzeller, Taryn D. Treger, Heike Streitenberger, Barbara Ziegler, Sabrina Bausenwein, Christian Vokuhl, Conor Parks, Eva Jüttner, Susanne Gramlich, Karen Ernestus, Steven W. Warman, Jörg Fuchs, Jochen Hubertus, Dietrich von Schweinitz, Birgit Fröhlich, Norbert Jorch, Ralf Knöfler, Carsten Friedrich, Selim Corbacioglu, Michael C. Frühwald, Arnulf Pekrun, Dominik T. Schneider, Jörg Faber, Jana Stursberg, Markus Metzler, Nils Welter, Kathy Pritchard-Jones, Norbert Graf, Rhoikos Furtwängler, Sam Behjati, Manfred Gessler   +31 more
doaj   +1 more source

Tumor de Wilms del adulto

, 2015
Se presenta y se comenta un caso de un paciente de 24 años con un tumor de Wilms en el adulto, así como el diagnóstico positivo y diferencial y la terapéutica empleada con mayor frecuencia en esta enfermedad.
Fernández Marichal, Fernando, Pila Pérez, Rafael, Rosales Torres, Pedro, Pila Peláez, Rafael, Vázquez Drake, Charles   +4 more
core  

Spontaneous rupture of adult Wilms' tumor

, 1989
Wilms' tumor is uncommon in adults, and spontaneous retroperitoneal hemorrhage as the presenting sign of renal malignancy also is rare. A 22-year-old man with spontaneous rupture of a Wilms' tumor, who died within 5 months, is described. The factors that
Heyns C.F., Rossouw D.J.
core  

EXTRARENAL WILMS' TUMOR: A RARE CASE PRESENTATION

, 2013
Purpose: Wilms' tumor is the most common primary abdominal neoplasm arising in the kidney in the pediatric population. However, Wilms' tumor arising outside of the kidney (extrarenal Wilms' tumor) is a highly rare occurrence.
Kelley IV, James
core  

Poster Sessions

HemaSphere, Volume 10, Issue S1, June 2026.
wiley   +1 more source

Histopathological and immunohistochemical features of Wilms' tumor

, 1992
의학과/석사[한글] Wilms 종양은 유소아기에 흔한 원발성 악성종양의 하나로 후신발생모체(metanephrogenic blastema)의 미분화 세포에서 기원한다고 알려져 있다. 과거에는 치사율이 높은 종양이 었으나 수술, 항암화학요법 및 방사선 치료의 병합요법으로 2년 생존율이 80% 이상으로 향상되어 치료가능한 악성종양의 하나로 알려져 있다.
최윤정
core  

Publication Only

HemaSphere, Volume 10, Issue S1, June 2026.
wiley   +1 more source

AI-Assisted Preoperative Diagnosis of Wilms Tumor. [PDF]

Life (Basel)
Akay MA, Tatar OC, Tatar E, Demirsoy U, Anık Y, Yıldız GE, Varlıklı O.   +6 more
europepmc   +1 more source

Paraspinal Extrarenal Wilms Tumor Case Report and Review of Literature. [PDF]

Case Rep Pediatr
Barbaro JL, Borowicz VM, Klein BJ, Emanuel AJ.   +3 more
europepmc   +1 more source

Wilms tumor in adults-an unusual encounter: a case report. [PDF]

J Med Case Rep
Kolap N, Sonawane R, Baviskar M, Bhalghat M.   +3 more
europepmc   +1 more source