Literature DB >> 28365106

Nephron-sparing surgery in the treatment of pediatric renal cell carcinoma associated with Xp11.2 translocation/TFE3 gene fusions.

Chao Liu1, Weiping Zhang2, Hongcheng Song3.   

Abstract

PURPOSE: To investigate the safety and efficacy of nephron-sparing surgery (NSS) in the treatment of pediatric Xp11.2 translocation renal cell carcinoma (RCC).
METHODS: Clinical characteristics of 9 RCC children (7 males and 2 females) with Xp11.2 translocation who received NSS between January 1973 and December 2015 were retrospectively analyzed. The mean age was 7.8years (range: 4.5-13.5years). Xp11.2 translocation RCC was found in the left side in 4 patients and right in 5. 3 tumors were located in the upper pole of the kidney, 1 in the middle dorsal, 1 in the middle ventral and 4 in the lower pole. RCC presented with painless gross hematuria in 4 patients, abdominal mass in 1, and as an incidental finding by ultrasound examination in 4 patients. The mean course of hematuria was 3months (range: 1-7months). The mean tumor diameters were 3.7cm (range: 2.2-6.9cm).
RESULTS: All the patients received NSS with open transperitoneal approach. The mean operative time and estimated blood loss were 115min and 40ml, respectively. The time of renal pedicle clamping was 19-25min (mean: 21.5min). No complications (such as leakage of urine, prolonged drainage or secondary bleeding) were noted. No patients experienced local recurrence during the mean of 50.1-month follow-up (range: 13-117months). Intravenous urography (IVU) or contrast-enhanced CT was conducted at 6months after surgery which showed favorable kidney function in all patients.
CONCLUSION: Xp11.2 translocation RCC is a predominant pathological but biologically inert type of pediatric RCC. For Xp11.2 translocation RCC sized <4-7cm in diameter and located in one pole, NSS is safe and feasible. TYPE OF STUDY: Treatment Studies, LEVEL IV.
Copyright © 2017 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Children; Nephron-sparing surgery; Renal cell carcinoma; TFE3 gene fusion; Xp11.2 translocation

Mesh:

Substances:

Year:  2017        PMID: 28365106     DOI: 10.1016/j.jpedsurg.2017.03.052

Source DB:  PubMed          Journal:  J Pediatr Surg        ISSN: 0022-3468            Impact factor:   2.545


  3 in total

1.  Nephron-Sparing Surgery for Adult Xp11.2 Translocation Renal Cell Carcinoma at Clinical T1 Stage: A Multicenter Study in China.

Authors:  Ning Liu; Feng Qu; Qiancheng Shi; Wenyuan Zhuang; Wenliang Ma; Zhenhao Yang; Jing Sun; Wei Xu; Lihua Zhang; Ruipeng Jia; Linfeng Xu; Xiaozhi Zhao; Xiaogong Li; Gutian Zhang; Hongqian Guo; Dongmei Li; Weidong Gan
Journal:  Ann Surg Oncol       Date:  2020-07-06       Impact factor: 5.344

2.  Chemotherapy, transarterial chemoembolization, and nephrectomy combined treated one giant renal cell carcinoma (T3aN1M1) associated with Xp11.2/TFE3: A case report.

Authors:  Peng Wang; Xiao Zhang; Shuo-Han Shao; Fa Wu; Fei-Zhou Du; Jun-Feng Zhang; Zhi-Way Zuo; Rui Jiang
Journal:  World J Clin Cases       Date:  2022-10-06       Impact factor: 1.534

3.  Factors Associated with Survival From Xp11.2 Translocation Renal Cell Carcinoma Diagnosis-A Systematic Review and Pooled Analysis.

Authors:  Yuqing Wu; Saisai Chen; Minhao Zhang; Kuangzheng Liu; Jibo Jing; Kehao Pan; Lihua Zhang; Bin Xu; Xiaoming Lu; Ming Chen
Journal:  Pathol Oncol Res       Date:  2021-03-30       Impact factor: 3.201

  3 in total

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