TY - CHAP M1 - Book, Section TI - Wilms’ Tumor A1 - Bianchi, Diana W. A1 - Crombleholme, Timothy M. A1 - D'Alton, Mary E. A1 - Malone, Fergal D. Y1 - 2015 N1 - T2 - Fetology: Diagnosis and Management of the Fetal Patient, 2e AB - Key PointsWilms’ tumor is a common cause of renal neoplasms in children but is rarely diagnosed in utero.The main differential diagnosis in Wilms’ tumor is mesoblastic nephrosis.Wilms’ tumor may present in utero as part of Perlman syndrome (ascites, polyhydramnios, hepatomegaly, macrosomia, and Wilms’ tumor).Wilms’ tumor may present as part of recognized genetic conditions including Beckwith–Wiedemann syndrome, Denys-Drash syndrome, WAGR syndrome, Fanconi anemia, and Simpson–Golabi–Behmel syndrome.Excellent survival is achieved with current therapies including surgery, chemotherapy, and in some cases radiation therapy. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/29 UR - obgyn.mhmedical.com/content.aspx?aid=1106401140 ER -