• Behçet's syndrome is a multisystem disease complex, the major manifestations of which are oral and genital ulcers, arthritis, uveitis, and skin eruptions. Less frequently, CNS disturbances, colitis, thrombophlebitis, large-vessel vasculitis, and myocarditis occur. If renal involvement does occur, it is usually manifested by asymptomatic microhematuria and/or proteinuria. Recently, renal amyloidosis and focal necrotizing glomerulonephritis with immune complex deposition have been described. We describe a patient with Behçet's syndrome who experienced diffuse proliferative glomerulonephritis with epithelial cell crescent formation in 75% of glomeruli examined. Immune complexes were not identified. Renal function, impaired on admission, improved with no therapy.
(Arch Intern Med 140:713-714, 1980)
Olsson PJ, Gaffney E, Alexander RW, Mars DR, Fuller TJ. Proliferative Glomerulonephritis With Crescent Formation in Behcet's Syndrome. Arch Intern Med. 1980;140(5):713–714. doi:10.1001/archinte.1980.00330170129039
Customize your JAMA Network experience by selecting one or more topics from the list below.
Create a personal account or sign in to: