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MDCT and MR Urogram Spectrum of Congenital Anomalies of the Kidney and Urinary Tract Diagnosed in Adulthood
被引:8
|作者:
Surabhi, Venkateswar R.
[1
]
Menias, Christine O.
[2
]
George, Verghese
[1
]
Matta, Eduardo
[1
]
Kaza, Ravi K.
[3
]
Hasapes, Joseph
[1
]
机构:
[1] Univ Texas Hlth Sci Ctr Houston, Dept Radiol, Houston, TX 77030 USA
[2] Mayo Clin, Dept Radiol, Scottsdale, AZ USA
[3] Univ Michigan, Ctr Hlth, Dept Diagnost Radiol, Ann Arbor, MI 48109 USA
关键词:
congenital;
congenital anomalies of the kidneys and urinary tract;
CT urogram;
duplex collecting system;
MR urogram;
URETEROPELVIC JUNCTION OBSTRUCTION;
RENAL AGENESIS;
SYSTEM URETEROCELES;
YOUNG-ADULTS;
CHILDREN;
MEGACALYCOSIS;
MANAGEMENT;
VESSELS;
DISEASE;
CALCULI;
D O I:
10.2214/AJR.14.12867
中图分类号:
R8 [特种医学];
R445 [影像诊断学];
学科分类号:
1002 ;
100207 ;
1009 ;
摘要:
OBJECTIVE. Congenital anomalies of the kidneys and urinary tract (CAKUT) encompass a spectrum of anomalies that result from genetic, epigenetic, environmental, and molecular signal aberrations at key stages of urinary tract development. CAKUT can be seen incidentally on cross-sectional imaging of the abdomen or can be a cause for adult-onset chronic kidney disease, posing new challenges for nephrologists, urologists, and radiologists. CONCLUSION. Awareness of CAKUT and familiarity with their imaging findings permit optimal patient management and thorough workup to prevent hypertension and progression from CAKUT to renal failure. The purpose of this article is to review the cross-sectional imaging findings of CAKUT that may present in adulthood.
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页码:W294 / W304
页数:11
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