马蹄形多肾(三肾)1例。

A. Adekanmi, O. Atalabi, I. Ukachukwu
{"title":"马蹄形多肾(三肾)1例。","authors":"A. Adekanmi, O. Atalabi, I. Ukachukwu","doi":"10.5580/2ce7","DOIUrl":null,"url":null,"abstract":"Supernumerary kidney is a rare congenital anomaly of the urinary system with less than 100 cases documented in literatures worldwide. Very rarely documented is the fused supernumerary kidney and horseshoe component with unknown incidence, due to the rarity of this complex anomaly. We hereby present a rare case of complex renal anomalies of fused supernumerary kidneys with horseshoe component misdiagnosed as an abdominal tumour on ultrasound, incidentally discovered at Computed Tomography. Introduction Supernumerary kidneys are rare congenital anomaly of the urinary system with less than 100 cases documented in literatures worldwide. The true incidence is unknown due to the rarity of the anomaly and it is believed to be found in both sexes with equal frequency . Embryologically, supernumerary kidney is believed to results from abnormal division of the nephrogenic cord into two metanephric blastemas that eventually form two kidneys with partial or duplicated ureteral bud 3, this occurs during the period of urogenital system formation about the 5 to 7week of gestation. No racial predominance is documented in the literature. And most cases of supernumerary kidneys are discovered incidentally Diagnosis and treatment are commonly challenging due to the rarity of this anomaly, its varied presentation and sparse documentation in literatures . Though horseshoe kidneys are relatively common renal fusion anomaly with an incidence of about one in 400-800 live births. Coexisting supernumerary and horseshoe kidney are however very rarely documented","PeriodicalId":22526,"journal":{"name":"The Internet Journal of Radiology","volume":"9 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2013-01-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":"{\"title\":\"Supernumerary Kidney (Triple Kidney) With Horseshoe Component: A Case Report.\",\"authors\":\"A. Adekanmi, O. Atalabi, I. Ukachukwu\",\"doi\":\"10.5580/2ce7\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Supernumerary kidney is a rare congenital anomaly of the urinary system with less than 100 cases documented in literatures worldwide. Very rarely documented is the fused supernumerary kidney and horseshoe component with unknown incidence, due to the rarity of this complex anomaly. We hereby present a rare case of complex renal anomalies of fused supernumerary kidneys with horseshoe component misdiagnosed as an abdominal tumour on ultrasound, incidentally discovered at Computed Tomography. Introduction Supernumerary kidneys are rare congenital anomaly of the urinary system with less than 100 cases documented in literatures worldwide. The true incidence is unknown due to the rarity of the anomaly and it is believed to be found in both sexes with equal frequency . Embryologically, supernumerary kidney is believed to results from abnormal division of the nephrogenic cord into two metanephric blastemas that eventually form two kidneys with partial or duplicated ureteral bud 3, this occurs during the period of urogenital system formation about the 5 to 7week of gestation. No racial predominance is documented in the literature. And most cases of supernumerary kidneys are discovered incidentally Diagnosis and treatment are commonly challenging due to the rarity of this anomaly, its varied presentation and sparse documentation in literatures . Though horseshoe kidneys are relatively common renal fusion anomaly with an incidence of about one in 400-800 live births. Coexisting supernumerary and horseshoe kidney are however very rarely documented\",\"PeriodicalId\":22526,\"journal\":{\"name\":\"The Internet Journal of Radiology\",\"volume\":\"9 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2013-01-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"The Internet Journal of Radiology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.5580/2ce7\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Internet Journal of Radiology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5580/2ce7","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 2

摘要

多肾是一种罕见的泌尿系统先天性异常,在世界范围内文献记载的病例不足100例。由于这种复杂异常的罕见性,很少有文献记载的合并多生肾和马蹄部分的发病率未知。我们在此报告一例罕见的合并多生肾合并马蹄成分的复杂肾脏异常,在超声上误诊为腹部肿瘤,在计算机断层扫描中偶然发现。摘要多肾是泌尿系统罕见的先天性异常,在世界范围内文献记载的病例不足100例。由于这种异常的罕见性,真正的发病率尚不清楚,据信在两性中发现的频率相同。胚胎学上,多肾被认为是由于肾原索异常分裂为两个后肾母细胞,最终形成两个肾和部分或重复输尿管芽3,这种情况发生在妊娠5至7周左右的泌尿生殖系统形成时期。在文献中没有种族优势的记载。多数病例是偶然发现的,诊断和治疗通常具有挑战性,因为这种异常罕见,其表现多样,文献记载稀少。虽然马蹄肾是相对常见的肾融合异常,发生率约为400-800活产1例。然而,马蹄肾和多余肾共存的情况很少有记载
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Supernumerary Kidney (Triple Kidney) With Horseshoe Component: A Case Report.
Supernumerary kidney is a rare congenital anomaly of the urinary system with less than 100 cases documented in literatures worldwide. Very rarely documented is the fused supernumerary kidney and horseshoe component with unknown incidence, due to the rarity of this complex anomaly. We hereby present a rare case of complex renal anomalies of fused supernumerary kidneys with horseshoe component misdiagnosed as an abdominal tumour on ultrasound, incidentally discovered at Computed Tomography. Introduction Supernumerary kidneys are rare congenital anomaly of the urinary system with less than 100 cases documented in literatures worldwide. The true incidence is unknown due to the rarity of the anomaly and it is believed to be found in both sexes with equal frequency . Embryologically, supernumerary kidney is believed to results from abnormal division of the nephrogenic cord into two metanephric blastemas that eventually form two kidneys with partial or duplicated ureteral bud 3, this occurs during the period of urogenital system formation about the 5 to 7week of gestation. No racial predominance is documented in the literature. And most cases of supernumerary kidneys are discovered incidentally Diagnosis and treatment are commonly challenging due to the rarity of this anomaly, its varied presentation and sparse documentation in literatures . Though horseshoe kidneys are relatively common renal fusion anomaly with an incidence of about one in 400-800 live births. Coexisting supernumerary and horseshoe kidney are however very rarely documented
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信