Long-term remission of bilateral Wilms tumors that developed from premature separation of chromatids/mosaic variegated aneuploidy syndrome due to bilateral nephrectomy and peritoneal dialysis.
Kayo OchiaiAi YamadaYasuhiro KimotoHideaki ImamuraToshio IkedaMakoto MatsukuboSatoshi IeiriHiroshi MirotakiPublished in: Pediatric blood & cancer (2019)
We report a 38-month-old Japanese male with premature chromatid separation/mosaic variegated aneuploidy syndrome bearing biallelic BUB1B germline mutations who suffered from bilateral Wilms tumor. After right nephrectomy, dactinomycin monotherapy was administered for the left Wilms tumor; however, severe adverse reaction prevented the patient from receiving further chemotherapy. Left nephrectomy was then performed without postoperative chemotherapy. The patient survived for 15 months after bilateral nephrectomy without peritoneal relapse, metastasis of Wilms tumor, or the occurrence of rhabdomyosarcoma and maintained a good quality of life while receiving peritoneal dialysis at home.
Keyphrases
- peritoneal dialysis
- case report
- end stage renal disease
- robot assisted
- editorial comment
- chronic kidney disease
- patients undergoing
- locally advanced
- randomized controlled trial
- intellectual disability
- early onset
- rheumatoid arthritis
- open label
- dna damage
- squamous cell carcinoma
- clinical trial
- oxidative stress
- mass spectrometry
- dna repair
- rectal cancer