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儿童重复肾合并术前下节细胞肿瘤破裂 1 例报告并文献复习

Duplex kidney complicated with preoperative inferior nephroblastoma rupture in children: a case report and literature review.

机构信息

The Fourth Hospital of Baotou, Baotou, China.

Beijing Children's Hospital, No, 6 Nanlishi Road, Xicheng District, Beijing, 100000, China.

出版信息

BMC Pediatr. 2021 Oct 8;21(1):441. doi: 10.1186/s12887-021-02919-2.

Abstract

BACKGROUND

We admitted a child with a duplex kidney combined with preoperative rupture of nephroblastoma and used this case to discuss the clinical features and treatment of this disease.

CASE PRESENTATION

We retrospectively analyzed the clinical data of a 5-year-old girl with preoperative duplex kidney rupture combined with inferior nephroblastoma who was admitted to the Fourth Hospital of Baotou. In addition, we reviewed the relevant literature. The patient's details were as follows: weight, 17 kg; height, 108 cm; and body surface area, 0.7 m. Abdominal ultrasound for abdominal pain revealed the presence of a left-sided renal mass; enhanced abdominal computed tomography further confirmed it to be a left-sided duplex kidney measuring approximately 6 × 5 × 5 cm, with a rupture originating from the lower kidney. The PubMed database was searched from 2010 to 2020 for the terms "Wilms' tumor" and "Duplex" and "Wilms' tumor" and "Rupture." The treatment plan was preoperative chemotherapy (vincristine/dactinomycin, VA regimen) + left kidney tumor radical surgery + postoperative chemotherapy (actinomycin-D/VCR/doxorubicin, AVD regimen). Postoperative pathology revealed an International Society of Pediatric Oncology intermediate-risk stage-3 nephroblastoma (mixed type) in the left kidney. Literature review was performed with 71 cases meeting the set criteria with an aim to analyze and summarize the clinical characteristics and treatment of patients with ruptured nephroblastoma and duplex kidney combined with nephroblastoma.

CONCLUSIONS

To our knowledge, no previous studies have reported preoperative duplex kidney combined with nephroblastoma rupture. In patients with this condition, preoperative chemotherapy is recommended when the vital signs are stable and tumor resection can be performed after the tumor has shrunk to prevent secondary spread. If the patient's vital signs are unstable, emergency exploratory surgery is needed. If the nephroblastoma rupture is old and limited, surgery can be performed when the tumor size is small.

摘要

背景

我们收治了一例合并术前破裂的肾母细胞瘤的重复肾患儿,并通过此病例探讨该病的临床特点和治疗方法。

病例介绍

我们回顾性分析了包头市第四医院收治的 1 例术前重复肾破裂合并下极肾母细胞瘤患儿的临床资料,并复习相关文献。患儿详细情况如下:体重 17kg,身高 108cm,体表面积 0.7m。腹痛行腹部超声检查发现左肾占位;增强腹部 CT 进一步证实为左侧重复肾,大小约 6cm×5cm×5cm,下极起源处破裂。以“Wilms 瘤”和“Duplex”、“Wilms 瘤”和“Rupture”为检索词,在 PubMed 数据库中检索 2010 年至 2020 年的相关文献。治疗方案为术前化疗(长春新碱/放线菌素 D,VA 方案)+左肾肿瘤根治术+术后化疗(放线菌素 D/VCR/多柔比星,AVD 方案)。术后病理示左侧肾脏为国际小儿肿瘤学会中危 3 期(混合性)肾母细胞瘤。通过检索并纳入 71 例符合标准的文献,对破裂型肾母细胞瘤合并重复肾的临床特点和治疗进行分析总结。

结论

据我们所知,目前尚无术前重复肾合并肾母细胞瘤破裂的相关报道。对于此类患者,当生命体征稳定,肿瘤缩小可切除时,建议行术前化疗;若生命体征不稳定,则需行急诊探查术。如果肿瘤破裂时间较长且局限,肿瘤较小时可手术治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9547/8499532/44759c564298/12887_2021_2919_Fig1_HTML.jpg

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