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Posterior reversible encephalopathy syndrome in a patient with hepatitis B induced type 1 membranoproliferative
Vishwanath Sathyanarayanan1, Abdul Razak, Girish Narayan
1Department of Medicine, Kasturba Medical College, # 1, OPD Block, Manipal 576104, Karnataka, India. docvishu@gmail.com
Abstract:
Posterior reversible encephalopathy syndrome (PRES) is a rare complication of nephrotic syndrome and corticosteroid therapy. Here, we discuss an 18 year old man with type 1 membranoproliferative glomerulonephritis (MPGN) secondary to hepatitis B infection who developed posterior leukoencephalopathy while on therapy with lamivudine and prednisone. He developed seizures and vision loss. He also had hypertension, but no sudden elevation was recorded at any time. Magnetic resonance imaging revealed patchy areas of altered signal intensity involving cortical gray and subcortical white matter in the bilateral frontoparietal regions, occipital cortices, temporal cortices and cerebellar hemispheres, and hyperintensity on T2W and FLAIR sequences. Tapering of prednisone and controlling hypertension resulted in clinical improvement within a few days, and in a month MRI was normal. Diagnosing PRES requires a high index of suspicion when treating similarly susceptible patients. PRES as a complication during the treatment of MPGN secondary to hepatitis B has, to our knowledge, never been reported previously in the literature.
Insights
Posterior reversible encephalopathy syndrome (PRES) is a rare complication. This case highlights PRES in a patient with hepatitis B-related membranoproliferative glomerulonephritis treated with prednisone, emphasizing diagnostic vigilance.
Area of Science:
- Neurology
- Nephrology
- Infectious Diseases
Background:
- Posterior reversible encephalopathy syndrome (PRES) is a rare neurological complication.
- It is often associated with nephrotic syndrome and corticosteroid therapy.
Observation:
- An 18-year-old male with hepatitis B-associated type 1 membranoproliferative glomerulonephritis (MPGN) developed PRES.
- Symptoms included seizures and vision loss, with hypertension but no acute elevation.
- MRI showed characteristic white matter changes in the brain.
Findings:
- Treatment involved tapering prednisone and managing hypertension.
- Clinical improvement occurred within days, with complete MRI normalization in one month.
- This represents a previously unreported association of PRES with MPGN secondary to hepatitis B.
Implications:
- Highlights the importance of high clinical suspicion for PRES in susceptible patients.
- Suggests a potential link between hepatitis B, MPGN, and PRES under specific treatments.
- Underscores the need for careful monitoring during immunosuppressive therapy for glomerulonephritis.
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