Presentation
History withheld.
Patient Data
Age: 20 years
Gender: Male
From the case:
Autosomal recessive polycystic kidney disease
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Markedly enlarged both kidneys eliciting diffuse abnormal high parenchymal signal secondary to numerous corticomedullary miccorcysts with loss of corticomedullary differentiation and multiple scattered small parenchymal macrocysts.
Case Discussion
The patient had a history of genetically proven autosomal recessive polycystic kidney disease and renal failure since the age of 13 year old.
Autosomal recessive polycystic kidney disease (ARPKD) is the recessive form of polycystic kidney disease.