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Updated: Feb 6, 2026

Imaging Features of Systemic Sclerosis-Associated Interstitial Lung Disease
Published on: June 16, 2020
Interstitial nephritis: Two pediatric cases with atypical radiological features.
Joseph Connors1, Rachel Aronov1, Laura Malaga-Dieguez1
1Division of Nephrology, Department of Pediatrics, Department of Radiology and Department of Pathology, NYU Langone Health, New York, NY 10016, USA.
Interstitial nephritis (IN) in children is rare and has no proven therapy. Recognizing unusual kidney imaging may aid early diagnosis and prevent confusion with other serious conditions.
Area of Science:
- Pediatric Nephrology
- Renal Pathology
- Medical Imaging
Background:
- Interstitial nephritis (IN) is an uncommon pediatric kidney disease with diverse causes like infections, medications, and autoimmune conditions.
- Current therapeutic options for IN remain limited, posing significant challenges in management.
- This study focuses on rare cases of IN presenting with atypical sonographic findings in pediatric patients.
Observation:
- Two pediatric cases of biopsy-proven interstitial nephritis were analyzed.
- One case exhibited granulomatous features and unique bilateral renal mass-like lesions on ultrasound.
- The other case presented with distinct, albeit less common, sonographic abnormalities.
Findings:
- Despite thorough investigation, the specific etiology of IN could not be determined in either case.
- One patient with atypical IN developed end-stage kidney disease (ESKD).
- The second patient is undergoing initial treatment for IN.
Implications:
- Atypical sonographic findings in pediatric IN can mimic neoplastic or infectious processes, potentially delaying diagnosis.
- Early recognition of these unusual imaging features is crucial for timely intervention and management.
- Further research into the imaging characteristics of pediatric IN may improve diagnostic accuracy and patient outcomes.
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