Presentation
Primary hyperoxaluria and end-stage renal disease. Persistent pus drainage through a right lower quadrant cutaneous orifice after removal of a rejected transplanted kidney.
Patient Data
Age: 35 years
Gender: Female
From the case:
Post renal transplant sinus tract (CT fistulography)
Download
Info
- large sinus tract starts from the RLQ orifice traversing the right paracolic space with communication to the right psoas muscle
- bilateral medullary and cortical nephrocalcinosis
- large hyperdense stone along with right kidney mid to upper pole
- diffuse bony sclerosis
Case Discussion
Primary hyperoxaluria is a rare autosomal recessive inborn error of metabolism that leads to elevation of oxalate in serum and urine and characterises by calcium oxalate crystal deposition in multiple organ systems (oxalosis).
Unable to process the form. Check for errors and try again.