首页|伴BRAF V600E基因突变的儿童后肾间质瘤1例并文献复习

伴BRAF V600E基因突变的儿童后肾间质瘤1例并文献复习

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对2022年6月郑州大学第一附属医院收治的1例伴BRAF V600E基因突变的儿童后肾间质瘤(MST)患儿的临床资料进行回顾性分析,并进行文献复习。患儿,女,2岁,因发现左侧腹部肿物就诊,肿瘤长径10。5 cm。行左侧肾根治性切除术,术后病理提示MST。镜下,肿瘤缺乏包膜,膨胀性生长为主,肿瘤细胞呈梭形或星状,富细胞区核分裂易见。肿瘤内部可见发育不良的血管;血管及内陷肾小管周围肿瘤细胞呈洋葱皮样排列。免疫组织化学染色CD34阳性,荧光PCR法检测到BRAF V600E突变阳性。文献检索相关病例报道共21篇,其中英文16篇、中文5篇,结合本研究1例,共纳入58例MST患儿,年龄2 d至15岁,中位年龄为2岁。除2例性别不明外,男女比例约为1。4∶1。0。MST多数无症状,肿瘤大小平均5。3 cm。肿瘤细胞CD34呈不同程度阳性表达。8例行BRAF V600E突变检测,均为阳性。58例患儿接受肾切除术,其中7例患儿辅助放化疗,随访0~156个月,1例死亡,1例复发。MST是临床罕见的肾脏良性间质瘤,BRAF V600E突变见于多种恶性肿瘤。本研究为国内首次对MST病例进行BRAF V600E基因突变的报道,并指出了 BRAF突变的分子检测对MST准确诊断的重要性。
Metanephric stromal tumor in children with BRAF V600E gene mutation:a case report and literature review
The clinical data of one child with metanephric stromal tumor(MST)and BRAF V600E gene mutation admitted to the First Affiliated Hospital of Zhengzhou University in June 2022 was analyzed retrospectively.Literature was reviewed.The patient,a 2-year-old girl,was diagnosed with a tumor in the left abdomen.The maximum diameter of the tumor was 10.5 cm.A radical nephrectomy was performed on the left kidney,and postoperative pathology revealed MST.Microscopically,the tumor had no envelope and exhibited expansive growth.The tumor cells were fusiform or stellate,and nuclear division was visible in the cell-rich region.Dysplastic blood vessels were seen inside the tumor.The tumor cells around the blood vessels and invaginated renal tubules were arranged like onion skin.CD34 was detected positive by immunohistochemical staining,and BRAF V600E mutation was also detected positive by fluorescent polymerase chain reaction.A total of 21 relevant case reports were retrieved,including 16 in English and 5 in Chinese.Fifty-eight MST patients,including the one in this report were analyzed.These patients were aged 2 days to 15 years,with a median age of 2 years.Except for 2 patients with unknown sex,the ratio of male to female was about 1.4∶:1.0.Most MST patients were asymptomatic,with an average tumor size of 5.3 cm.The tumor cell CD34 showed positive expression in different degrees.Eight patients received the BRAF V600E mutation detection,and the results were all positive.Fifty-eight patients underwent nephrectomy and were followed up for 0-156 months,of which 7 patients were assisted with radiotherapy and chemotherapy.During the follow-up,1 patient died,and 1 patient had a relapse.MST is a rare benign renal stromal tumor.BRAF V600E mutations are detected in a variety of malignancies.This paper is the first to report MST with BRAF V600E mutation in China and points out the importance of molecular detection of BRAF mutation for accurate diagnosis of MST.

PathologyMetanephric stromal tumourChildBRAF V600E gene

毛舒婷、王叨、李白、刘姗姗、魏林林、苏淑芳、徐岩、马亚南、周歌、刘玉峰

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郑州大学第一附属医院儿科,郑州 450052

病理 后肾间质瘤 儿童 BRAF V600E基因

2024

中华实用儿科临床杂志
中华医学会

中华实用儿科临床杂志

CSTPCD北大核心
影响因子:1.5
ISSN:2095-428X
年,卷(期):2024.39(4)
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