Rapidly Progressive Glomerulonephritis Associated With IgA Nephropathy and C3 Deposits in a Patient With Chronic Hepatitis B.

Jennifer Wiese, Nayiri A Derian, M'hamed Turki, Tejas Joshi, Ahlim Alsanani, Anjali Satoskar
Author Information
  1. Jennifer Wiese: Internal Medicine, Marshall University Joan C. Edwards School of Medicine, Huntington, USA.
  2. Nayiri A Derian: Internal Medicine, Marshall University Joan C. Edwards School of Medicine, Huntington, USA.
  3. M'hamed Turki: Gastroenterology, Marshall University Joan C. Edwards School of Medicine, Huntington, USA.
  4. Tejas Joshi: Gastroenterology and Hepatology, Marshall University Joan C. Edwards School of Medicine, Huntington, USA.
  5. Ahlim Alsanani: Nephrology, Marshall University Joan C. Edwards School of Medicine, Huntington, USA.
  6. Anjali Satoskar: Pathology, The Ohio State University College of Medicine, Columbus, USA.

Abstract

Hepatitis B-associated glomerulonephritis (GN) has been recognized for decades. However, only a few cases of IgA nephropathy (IgAN) in a setting of rapidly progressive glomerulonephritis (RPGN) associated with chronic hepatitis B virus (HBV) have been described. Herein, we report the case of a 42-year-old Asian female with a past medical history significant for chronic HBV on entecavir, hypertension, chronic kidney disease, and newly diagnosed breast cancer, who underwent elective bilateral mastectomy and breast augmentation. Post-operatively, she developed non-oliguric acute kidney injury and proteinuria. Renal biopsy revealed active focal crescentic and necrotizing GN with IgA and C3 deposits. Systemic autoimmune-associated and other infection-related GN were ruled out. IgAN in a setting of RPGN associated with chronic HBV was suspected.

Keywords

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Word Cloud

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