The disease is a hereditary disease, and inherited a great chance, but because of mixed and other diseases, this will bring a lot to the treatment of polycystic kidney unfavorable factors, then how because of it! I went into the polycystic kidney disease World disease it!
How clever to identify polycystic kidney disease too!
How clever to identify polycystic kidney disease too!
1. Identification of renal angiomyolipoma, hamartoma with characteristic B-, cT image, because much of the fat content of hamartoma show different B-image. Fat tissue in the B-hyperechoic light group, while in CT CT-value is negative. The characteristic features of polycystic kidney completely different. Hamartoma single kidney onset common, rare renal hamartoma. 2, and renal water identification, when renal water, IVP and B ultrasound, CT examination of polycystic kidney completely different images and, if necessary, RP inspection, identification difficult.
3, and multiple cysts in the kidneys identification, multiple renal cysts course is often longer, depending on renal function in cyst size, number and oppression caused by the kidney and normal renal parenchyma different majority, cysts usually in the renal parenchyma rim. The number of CT under multiple cysts in polycystic kidneys much less compared, and the majority of normal renal parenchyma, renal parenchymal cysts usually in the outer edge.
4, with the identification of simple renal cysts, simple renal cysts are often single kidney, a single cyst, cysts can be no significant long-term change. If no cause for the renal collecting system of oppression, has little effect on renal function, you can check with polycystic identified by IVP, CT and so on.
The above information on how to identify polycystic kidney disease clever! Made a detailed presentation, if you have a question about this or some method of Health Care presented words. You can consult our experts, we wish you a speedy recovery.
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