Presentation
Routine scan after first episode of UTI.
Patient Data
Age: 4 months
Gender: Female
From the case:
Multicystic dysplastic kidney
{"current_user":null,"step_through_annotations":true,"access":{"can_edit":false,"can_download":true,"can_toggle_annotations":true,"can_feature":false,"can_examine_pipeline_reports":false,"can_pin":false},"extraPropsURL":"/studies/9359/annotated_viewer_json?lang=us"}
Multiple cysts of varying sizes replacing the entire right renal parenchyma. No obvious communication with pelvicalyceal system is evident.
Normal left kidney.
Case Discussion
Multicystic dysplastic kidney is a pediatric cystic renal disease, which is usually diagnosed in-utero. This case depicts post-natal presentation of a unilateral multicystic dysplastic kidney (MCDK).
Unable to process the form. Check for errors and try again.