References in periodicals archive ?
9 Mikami T, Hada T, Chosa N, Ishisaki A, Mizuki H, Takeda Y: Expression of Wilms' tumor 1 (WT1) in oral squamous cell carcinoma.
Wilms' tumor is one of the most common intraabdominal malignancies in pediatric patients, but continues to be a rare occurrence in adult patients.
Arisoy, "Spinal cord compression and lung metastasis of Wilms' tumor in a pregnant adolescent," Urology, vol.
Shamberger et al., "Ureteral extension in Wilms' tumor: a report from the National Wilms' Tumor Study Group (NWTSG)," Journal of Pediatric Surgery, vol.
Neuberg et al., "Characteristics and outcome of children with Beckwith-Wiedemann syndrome and Wilms' tumor: a report from the National Wilms Tumor Study Group," Journal of Clinical Oncology, vol.
Ravshanova et al., "Efficacy and toxicity of ICE/CCE chemotherapy with or without GMCSF in relapsed or refractory Wilms' tumor. A single institution study," International Journal of Pediatric Hematology/Oncology, vol.
Wilms' tumor imitates the classic triphasic aspect of the embryonic kidney histology (blastema, epithelia, and stroma), the most characteristic pattern.
Defective chromosome segregation and telomere dysfunction in aggressive Wilms' tumors. Clin Cancer Res 2007;13 (22 Pt 1):6593-602.
This excellent outcome results from collaborative efforts among pediatric surgeons, pathologists, radiologists and oncologists.2 The two largest collaborative groups that have studied the optimal management of Wilms' tumor are the Children's Oncology Group (COG) and the International Society of Pediatric Oncology (SIOP).2 The COG recommends primary surgery before an adjuvant treatment except in specific circumstances such as synchronous bilateral disease.
Title: Bilateral Wilms' Tumor and Nephron-Sparing Surgery: A Case Report