Membranous glomerulonephropathy in a patient with bullous pemphigoid
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Updated: Mar 2, 2026

Granulocyte-dependent Autoantibody-induced Skin Blistering
Published on: October 12, 2012
Misa Ikeda1, Hirokazu Honda2,3, Naoto Kobayashi1
1Division of Nephrology, Department of Medicine, School of Medicine, Showa University, Tokyo, Japan.
Abstract:
Bullous pemphigoid (BP) is a common autoimmune blistering disease that can be complicated by autoimmune disorders. We describe a patient with BP who developed membranous glomerulonephropathy (MN). Proteinuria decreased during the clinical course as anti-BP180 antibody titers decreased. This finding suggested an association between the pathogenesis of these two diseases in terms of immunological disorders.
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