Multicystic dysplastic kidney: Difference between revisions

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==Overview==


'''Multicystic dysplastic kidney''' (MCDK) is a condition that results from the malformation of the [[kidney]] during fetal development.  The kidney consists of irregular cysts of varying sizes and has zero function.
'''Multicystic dysplastic kidney''' (MCDK) is a condition that results from the malformation of the [[kidney]] during fetal development.  The kidney consists of irregular cysts of varying sizes and has zero function.

Revision as of 05:28, 12 March 2009

Multicystic dysplastic kidney
ICD-10 Q61.4 (EUROCAT Q61.40-Q61.41)
eMedicine radio/458 

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Overview

Multicystic dysplastic kidney (MCDK) is a condition that results from the malformation of the kidney during fetal development. The kidney consists of irregular cysts of varying sizes and has zero function.

Epidemiology

In the United States, the incidence of MCDK is estimated to be 1 in every 2400 live births.[1]

Diagnosis

MCDK is usually diagnosed by ultrasound examination before birth.

Diagnostic Findings

Ultrasonography

  • Mass of non-communicating cysts of variable size.
  • Unlike severe hydronephrosis, in which the largest cystic structure (the renal pelvis) lies in a central location and is surrounded by dilated calices, in multicystic dysplastic kidney the cyst distribution shows no recognizable pattern.
  • Dysplastic, echogenic parenchyma may be visible between the cysts, but no normal renal parenchyma is seen.



Treatment

MCDK is not treatable. However, the patient is observed periodically for the first few years during which ultrasounds are generally taken to ensure the healthy kidney is functioning properly and that the unhealthy kidney is not causing adverse effects.

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