Malrotated right supernumerary kidney: Case report of a rare anomaly

被引：2

作者：

Al Dandan, Omran ^{[1
]}

Hassan, Ali ^{[1
]}

Almutairi, Afnan ^{[2
]}

Alakloby, Esra ^{[2
]}

Fadaak, Kamel ^{[3
]}

机构：

[1] Imam Abdulrahman Bin Faisal Univ, King Fahd Hosp Univ, Dept Radiol, Al Khobar, Saudi Arabia

[2] Imam Abdulrahman Bin Faisal Univ, King Fahd Hosp Univ, Dept Med, Al Khobar, Saudi Arabia

[3] Imam Abdulrahman Bin Faisal Univ, King Fahd Hosp Univ, Dept Urol, Al Khobar, Saudi Arabia

来源：

UROLOGY CASE REPORTS | 2019年 / 26卷

关键词：

Supernumerary kidney; Congenital anomaly; Malrotation;

D O I：

10.1016/j.eucr.2019.100966

中图分类号：

R5 [内科学]; R69 [泌尿科学（泌尿生殖系疾病）];

学科分类号：

1002 ; 100201 ;

摘要：

Supernumerary Kidney is a one of the rarest congenital renal anomalies with less than 100 cases reported in the literature. This accessory kidney has its own collecting system, vascular supply and well-defined capsule. We report a case of 18-year-old lady with a history of vague intermittent abdominal pain and has palpable abdominal mass who was found to have malrotated right supernumerary kidney with pelviureteric junction obstruction.

引用

页数：3

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