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Updated: Aug 29, 2025

Neuronavigation and Laparoscopy Guided Ventriculoperitoneal Shunt Insertion for the Treatment of Hydrocephalus
Published on: October 14, 2022
A girl with membranous nephropathy associated with ventriculoperitoneal shunt infection
Midori Awazu1,2, Maiko Miyahara3, Michiko Chiga3
1Department of Pediatrics, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo, Japan. midoriawazu@gmail.com.
Abstract:
Glomerulopathy associated with shunt infection is commonly membranoproliferative glomerulonephritis, whereas the causative organisms of secondary membranous nephropathy are usually viruses. We report a case of membranous nephropathy associated with shunt infection. The patient was born at 29-week gestation with a birth weight of 1178 g. Ventriculoperitoneal shunt surgery had been performed for congenital hydrocephalus. Thereafter, she had experienced seven shunt infections. At the age 13 years, proteinuria was detected in a school urinary screening. Urinalysis at our hospital demonstrated 3 + protein and 3 + blood. Laboratory testing demonstrated a serum creatinine 0.5 m/dl, albumin 2.5 g/dl, C-reactive protein (CRP) 13.7 mg/dl, and C3 182 mg/dl. Prior to repeat urinalysis, the patient developed vomiting and was admitted with suspected shunt infection. On admission, her body temperature was 36.0 ºC. Physical examination was unremarkable other than small stature and a palpable mass in the left upper quadrant. Urinalysis demonstrated 2 + protein and 1 + blood with no cells or casts. The urinary protein excretion was 3 g/day. Abnormal laboratory tests included erythrocyte sedimentation rate 102 mm/hr, CRP 11.67 mg/dl, IgG 2442 mg/dl, C3 177 mg/dl, and C4 44 mg/dl. Antibiotic therapy was initiated for a presumptive diagnosis of shunt infection and the shunt catheter was removed. Cultures obtained after antibiotic administration were negative. Proteinuria persisted after control of the shunt infection. Histology of a renal biopsy demonstrated membranous nephropathy with diffuse granular IgG staining and subepithelial deposits. Three possible pathomechanisms for her membranous nephropathy were considered.
Insights
This case study presents a rare instance of membranous nephropathy linked to shunt infection in a young patient. It highlights the need to consider unusual causes of glomerulopathy beyond typical associations.
Area of Science:
- Nephrology
- Pediatric Nephrology
- Infectious Diseases
Background:
- Shunt infections are typically associated with membranoproliferative glomerulonephritis.
- Secondary membranous nephropathy is usually caused by viral infections.
Observation:
- A 13-year-old patient with a history of congenital hydrocephalus and multiple ventriculoperitoneal shunt infections presented with significant proteinuria and hematuria.
- Despite successful treatment of a suspected shunt infection, persistent proteinuria and laboratory findings suggestive of glomerulonephritis were noted.
Findings:
- Renal biopsy confirmed membranous nephropathy with characteristic subepithelial IgG deposits.
- Cultures were negative, and proteinuria persisted after shunt infection control, suggesting a complex etiology.
Implications:
- This case expands the known spectrum of kidney disease associated with shunt infections.
- It underscores the importance of thorough investigation for glomerulonephritis in patients with recurrent shunt infections, even when typical pathogens or presentations are absent.
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