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Use of Ultra-high Field MRI in Small Rodent Models of Polycystic Kidney Disease for In Vivo Phenotyping and Drug Monitoring
Published on: June 23, 2015
Multicystic nephroma: a rare entity
Smriti Agnihotri1, Nilima Jeebun, Poonam Ramputty
1Department of Pathology, SSR Medical College, Belle Rive - Mauritius. smriti_agnihotri@yahoo.co.uk
Journal of Nephrology
|June 27, 2009
Summary
Multicystic nephroma, a rare kidney tumor, typically presents as a unilateral renal mass. This case highlights a pediatric diagnosis of multicystic nephroma confirmed via histology after in utero detection.
Area of Science:
- Pediatric Nephrology
- Renal Pathology
- Diagnostic Imaging
Background:
- Multicystic nephroma is an uncommon benign renal neoplasm.
- It typically manifests as a unilateral renal mass with multiple cysts separated by septa.
Observation:
- A 2-year-old boy was diagnosed prenatally with a cystic abdominal lesion.
- Routine antenatal ultrasonography identified the anomaly during pregnancy.
Findings:
- The patient underwent a nephrectomy for the renal mass.
- Histological examination confirmed the diagnosis of multicystic nephroma.
Implications:
- This case underscores the importance of antenatal ultrasonography in detecting congenital renal anomalies.
- Early diagnosis facilitates timely surgical intervention and management of pediatric renal tumors.
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