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Urographic visualization of multicystic kidneys
The Journal of Urology
|January 1, 1977
Summary
Multicystic kidneys typically lack visible renal tissue on excretory urography. However, recent cases demonstrate contrast medium visualization of renal parenchyma in pathologically confirmed multicystic kidneys.
Area of Science:
- Nephrology
- Radiology
- Medical Imaging
Background:
- Multicystic dysplastic kidney (MCDK) is a congenital anomaly.
- Traditionally, MCDK is characterized by non-functioning renal parenchyma.
- Radiographic visualization of renal parenchyma in MCDK is considered absent.
Purpose of the Study:
- To report on the radiographic visualization of renal parenchyma in pathologically confirmed cases of multicystic kidneys.
- To challenge the classical understanding of MCDK on excretory urography.
Main Methods:
- Retrospective review of 4 cases with pathologically confirmed multicystic kidneys.
- Analysis of excretory urograms to assess contrast medium concentration and visualization of renal tissue.
Main Results:
- Radiographic visualization of renal parenchyma was achieved in 4 cases of typical multicystic kidneys.
- Sufficient concentration of contrast medium allowed for visualization of renal tissue.
Conclusions:
- The findings suggest that functioning renal parenchyma can be visualized in some cases of multicystic kidneys.
- Excretory urography may reveal renal tissue in MCDK under specific conditions of contrast enhancement.