Focal segmental glomerulosclerosis with intramembranous vesicle-like microstructures and podocytic infolding lesion |
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Authors: | Shunsuke Yamada Kohsuke Masutani Ritsuko Katafuchi Yoshihide Fujigaki Yoshinori Muranaka Kazuhiko Tsuruya Mitsuo Iida |
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Institution: | (1) Department of Medicine and Clinical Science, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka 812-8582, Japan;(2) Division of Internal Medicine, National Fukuoka Higashi Medical Center, Koga, Japan;(3) The First Department of Medicine, Hamamatsu University School of Medicine, Hamamatsu, Japan;(4) Equipment Center, Hamamatsu University School of Medicine, Hamamatsu, Japan |
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Abstract: | A 42-year-old woman was admitted to Kyushu University hospital because of 6 months' history of bilateral leg edema. Upon admission,
ascites and pleural effusion as well as systemic edema were noted. Laboratory tests revealed hypoalbuminemia of 1.5 g/dl and
massive proteinuria of 10 g/day. She was diagnosed with nephrotic syndrome. Renal biopsy revealed diffuse thickening of the
glomerular basement membrane (GBM) and a crescent-like extracapillary lesion with segmental sclerosis in four of 11 glomeruli.
Immunoglobulins and complements were negative by immunofluorescence examination. Therefore, we diagnosed this as focal segmental
glomerulosclerosis (FSGS) rather than membranous nephropathy. Using an electron microscope, we observed a thickening of the
GBM with numerous intramembranous vesicle-like microstructures and an infolding of the podocyte into the GBM. Since the microstructures
were partly demarcated by a unit membrane and some of them were located very closely to the infolded podocyte, we speculated
that the microstructures were derived from the podocyte. The unique electron microscopic finding of our case is a disease
entity rather than a reactive phenomenon. |
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Keywords: | Glomerular basement membrane Microstructure Podocytic infolding |
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