ArticleCureus2025
Membranoproliferative Glomerulonephritis Due to Hepatic Hydatid Disease.
Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Hydatid disease is a parasitic infection primarily involving the liver and is prevalent in Mediterranean and other endemic regions. Although commonly hepatic, its association with glomerular injury is extremely rare. We report the case of a 16-year-old male with a history of chronic cough and exposure to dogs who presented with generalized edema, macroscopic hematuria, and renal impairment. Laboratory evaluation confirmed nephrotic-range proteinuria, hypoalbuminemia, and impaired renal function. Renal biopsy revealed immune complex-mediated membranoproliferative glomerulonephritis (MPGN) with activation of the classical complement pathway. Imaging identified hepatic cystic lesions, and hydatid serology was positive. The patient underwent surgical excision of the cyst followed by albendazole therapy. Postoperatively, proteinuria decreased to 1.78 g/24 h by day 7 and resolved completely by day 30, with normalization of renal function and serum albumin levels. This case highlights the importance of considering hydatid disease in the differential diagnosis of unexplained nephrotic syndrome in endemic regions, as early recognition and appropriate management can lead to full recovery.
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