• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

印度儿童肾母细胞瘤的前驱病变:一项多机构研究。

Precursor lesions of Wilms' tumor in Indian children: a multiinstitutional study.

作者信息

Mishra K, Mathur M, Logani K B, Kakkar N, Krishna A

机构信息

Department of Pathology, University College of Medical Sciences and Guru Teg Bahadur Hospital, Shahdara, Delhi, India.

出版信息

Cancer. 1998 Nov 15;83(10):2228-32.

PMID:9827730
Abstract

BACKGROUND

Studies regarding different ethnic populations of children with Wilms' tumor (WT) in the U. S. have shown differences between age and gender incidence and the type of its precursor lesions (nephrogenic rests). To the authors' knowledge there are few reports in the literature regarding nephrogenic rests in a large number of cases from other parts of the world.

METHODS

In this study, histopathology sections from 127 WTs were pooled from the archives of 4 institutions in northern India and studied for the incidence of nephrogenic rests. Their incidence also was cross-correlated with patient age gender, and tumor morphology.

RESULTS

Significantly, the complete absence of perilobar nephrogenic rests was observed in all cases. Intralobar rests were associated with 45.3% of WTs and were observed predominantly with a triphasic histologic pattern and a relatively lower incidence of anaplasia compared with reports in the Western literature (1.5% vs. 4.5%). A lower median age of 2.5 years with a peak in the first 2 years of life was consistent with reported studies in Asian children. The male gender preponderance was in contrast to the equal male to female ratio reported in Western cases.

CONCLUSIONS

The type of nephrogenic rests present in Indian children was noted to be different from that in children reported in the Western literature. Differences also existed with regard to the age and gender incidence of children with WT and its morphologic pattern, possibly due to the different genetic nature of the tumor. However, this theory requires confirmation by large epidemiologic and genetic studies.

摘要

背景

关于美国不同种族儿童肾母细胞瘤(WT)的研究表明,年龄、性别发病率及其前驱病变(肾源性残留)类型存在差异。据作者所知,文献中鲜有关于世界其他地区大量病例肾源性残留的报道。

方法

本研究汇总了印度北部4家机构档案中的127例WT组织病理学切片,研究肾源性残留的发生率。其发生率还与患者年龄、性别及肿瘤形态进行了交叉关联分析。

结果

值得注意的是,所有病例均未观察到叶外周肾源性残留。叶内残留与45.3%的WT相关,主要表现为三相组织学模式,与西方文献报道相比,间变发生率相对较低(1.5%对4.5%)。2.5岁的较低中位年龄及出生后前2年的发病高峰与亚洲儿童的报道研究一致。男性占优势,这与西方病例报道的男女比例相等形成对比。

结论

印度儿童中存在的肾源性残留类型与西方文献报道的儿童不同。WT患儿的年龄、性别发病率及其形态模式也存在差异,这可能是由于肿瘤的不同遗传性质所致。然而,这一理论需要通过大规模的流行病学和遗传学研究来证实。

相似文献

1
Precursor lesions of Wilms' tumor in Indian children: a multiinstitutional study.印度儿童肾母细胞瘤的前驱病变:一项多机构研究。
Cancer. 1998 Nov 15;83(10):2228-32.
2
Inactivation of WT1 in nephrogenic rests, genetic precursors to Wilms' tumour.肾源性残留(Wilms瘤的遗传前体)中WT1的失活。
Nat Genet. 1993 Dec;5(4):363-7. doi: 10.1038/ng1293-363.
3
Wilms' tumor at the Children's Hospital of Eastern Ontario: 1990-2001.安大略东部儿童医院的肾母细胞瘤:1990 - 2001年
Can J Urol. 2004 Feb;11(1):2151-6.
4
Wilms' tumour in Malaysian children: a histopathological study of cases encountered at the University Hospital, Kuala Lumpur over a 22-year period.马来西亚儿童的肾母细胞瘤:对吉隆坡大学医院22年间收治病例的组织病理学研究
Malays J Pathol. 1992 Dec;14(2):111-5.
5
Microdissecting the genetic events in nephrogenic rests and Wilms' tumor development.剖析肾源性残留和肾母细胞瘤发生发展过程中的基因事件。
Am J Pathol. 1998 Sep;153(3):991-1000. doi: 10.1016/S0002-9440(10)65641-6.
6
Nephrogenic rests, nephroblastomatosis, and associated lesions of the kidney.肾源性残留、肾母细胞瘤病及肾脏相关病变
Radiographics. 1998 Jul-Aug;18(4):947-68. doi: 10.1148/radiographics.18.4.9672980.
7
Expression of MIB and BCL-2 in patients with nephrogenic rests with and without associated Wilms' tumors.伴有和不伴有相关肾母细胞瘤的肾源性残留患者中MIB和BCL-2的表达
Eur J Pediatr Surg. 2001 Apr;11(2):105-9. doi: 10.1055/s-2001-13783.
8
Nephrogenic rests in Wilms tumor patients with the Drash syndrome.患有德朗综合征的威尔姆斯瘤患者中的肾源性残留。
J Urol. 1991 Jun;145(6):1225-8. doi: 10.1016/s0022-5347(17)38582-8.
9
Imaging accuracy and incidence of Wilms' and non-Wilms' renal tumors in children.儿童肾母细胞瘤和非肾母细胞瘤性肾肿瘤的成像准确性及发病率
J Pediatr Surg. 2008 Jul;43(7):1301-7. doi: 10.1016/j.jpedsurg.2008.02.077.
10
Cytogenetic findings in Wilms' tumour: a single institute study.威尔姆斯瘤的细胞遗传学发现:单一机构研究。
Pathology. 2010 Dec;42(7):643-9. doi: 10.3109/00313025.2010.522171.

引用本文的文献

1
Inter-Ethnic Variations in the Clinical, Pathological, and Molecular Characteristics of Wilms Tumor.肾母细胞瘤临床、病理及分子特征的种族间差异
Cancers (Basel). 2024 Sep 1;16(17):3051. doi: 10.3390/cancers16173051.
2
Clinico-histopathological Profile of Primary Paediatric Intra-abdominal Tumours: a Multi-hospital-Based Study.原发性小儿腹腔内肿瘤的临床病理特征:一项多中心研究
Indian J Surg Oncol. 2021 Sep;12(3):517-523. doi: 10.1007/s13193-021-01365-x. Epub 2021 Jun 8.
3
Diagnostic utility of Wilms' tumour-1 protein (WT-1) immunostaining in paediatric renal tumours.
肾母细胞瘤-1蛋白(WT-1)免疫染色在小儿肾肿瘤中的诊断效用
Indian J Med Res. 2016 May;143(Supplement):S59-S67. doi: 10.4103/0971-5916.191776.
4
Immunohistochemical Expression of Ki67 and p53 in Wilms Tumor and Its Relationship with Tumor Histology and Stage at Presentation.Ki67和p53在肾母细胞瘤中的免疫组化表达及其与肿瘤组织学和初诊时分期的关系。
Patholog Res Int. 2016;2016:6123951. doi: 10.1155/2016/6123951. Epub 2016 Jan 20.
5
Wilms' tumor: biology, diagnosis and treatment.威尔姆斯瘤:生物学、诊断与治疗。
Transl Pediatr. 2014 Jan;3(1):12-24. doi: 10.3978/j.issn.2224-4336.2014.01.09.
6
Loss of heterozygosity at 11p13 and 11p15 in Wilms tumor: a study of 22 cases from India.肾母细胞瘤中11p13和11p15杂合性缺失:来自印度的22例病例研究
Pediatr Surg Int. 2013 Mar;29(3):223-7. doi: 10.1007/s00383-012-3254-8. Epub 2013 Jan 5.
7
Study of histopathological features and proliferation markers in cases of Wilms' tumor.肾母细胞瘤病例的组织病理学特征及增殖标志物研究
Indian J Med Paediatr Oncol. 2012 Apr;33(2):102-6. doi: 10.4103/0971-5851.99744.