PubMed, the Internet portal of biomedical and life sciences literature, indexed an interesting article, entitled Evolution of antiglomerular basement membrane glomerulonephritis into membranous glomerulonephritis. ( Pediatr Nephrol. 2007 Nov 13; ). Authors are Hecht N Omoloja A, Witte D et al., from the Department of Pediatrics, Wright State University Boonshoft School of Medicine, Dayton, OH, USA. Antiglomerular basement membrane glomerulonephritis (anti-GBM GN) is a rare disease characterized by autoantibodies to the alpha 3 chain of type IV collagen in the GBM. It is also known as Goodpasture’s syndrome when associated with pulmonary hemorrhage due to autoantibodies to the alpha 3 chain of type IV collagen also present in pulmonary alveoli. Even more rare is the evolution of anti-GBM GN into membranous nephropathy (MN). We report the management of a 9-year-old Caucasian girl with anti-GBM GN that evolved into MN and briefly review the literature. To access the full abstract of the article, click here.
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