Nephrotic syndrome with massive accumulation of type I and type III collagen in the glomeruli

Futoshi Yoshida, Yukio Yuzawa, Seiichi Matsuo, Hidekazu Shigematsu, Akira Ito, Chikao Yamazaki, Kazuo Yoshioka, Akira Ooshima

研究成果: Article

21 引用 (Scopus)

抄録

A 54-year-old woman with nephrotic syndrome underwent renal biopsy. By light microscopy, the glomerular capillary lumen was remarkably narrowed because of diffuse accumulation of Periodic acid Shiff (PAS) positive material along the glomerular capillary wall. By electron microscopy, collagenous fibers were observed in the mesangium and subendothelial area. The fibrous material reacted with antibodies against type I and III collagen but not with those against laminin or type IV collagen by an indirect immunofluorescence technique. This case seemed to be a case of collagenofibrotic glomerulonephropathy.

元の言語English
ページ(範囲)171-176
ページ数6
ジャーナルInternal Medicine
32
発行部数2
DOI
出版物ステータスPublished - 01-01-1993

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Collagen Type III
Nephrotic Syndrome
Collagen Type I
Periodic Acid
Collagen Type IV
Laminin
Indirect Fluorescent Antibody Technique
Microscopy
Electron Microscopy
Kidney
Biopsy
Light
Antibodies

All Science Journal Classification (ASJC) codes

  • Internal Medicine

これを引用

Yoshida, Futoshi ; Yuzawa, Yukio ; Matsuo, Seiichi ; Shigematsu, Hidekazu ; Ito, Akira ; Yamazaki, Chikao ; Yoshioka, Kazuo ; Ooshima, Akira. / Nephrotic syndrome with massive accumulation of type I and type III collagen in the glomeruli. :: Internal Medicine. 1993 ; 巻 32, 番号 2. pp. 171-176.
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abstract = "A 54-year-old woman with nephrotic syndrome underwent renal biopsy. By light microscopy, the glomerular capillary lumen was remarkably narrowed because of diffuse accumulation of Periodic acid Shiff (PAS) positive material along the glomerular capillary wall. By electron microscopy, collagenous fibers were observed in the mesangium and subendothelial area. The fibrous material reacted with antibodies against type I and III collagen but not with those against laminin or type IV collagen by an indirect immunofluorescence technique. This case seemed to be a case of collagenofibrotic glomerulonephropathy.",
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Yoshida, F, Yuzawa, Y, Matsuo, S, Shigematsu, H, Ito, A, Yamazaki, C, Yoshioka, K & Ooshima, A 1993, 'Nephrotic syndrome with massive accumulation of type I and type III collagen in the glomeruli', Internal Medicine, 巻. 32, 番号 2, pp. 171-176. https://doi.org/10.2169/internalmedicine.32.171

Nephrotic syndrome with massive accumulation of type I and type III collagen in the glomeruli. / Yoshida, Futoshi; Yuzawa, Yukio; Matsuo, Seiichi; Shigematsu, Hidekazu; Ito, Akira; Yamazaki, Chikao; Yoshioka, Kazuo; Ooshima, Akira.

:: Internal Medicine, 巻 32, 番号 2, 01.01.1993, p. 171-176.

研究成果: Article

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AU - Yoshida, Futoshi

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AU - Ito, Akira

AU - Yamazaki, Chikao

AU - Yoshioka, Kazuo

AU - Ooshima, Akira

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AB - A 54-year-old woman with nephrotic syndrome underwent renal biopsy. By light microscopy, the glomerular capillary lumen was remarkably narrowed because of diffuse accumulation of Periodic acid Shiff (PAS) positive material along the glomerular capillary wall. By electron microscopy, collagenous fibers were observed in the mesangium and subendothelial area. The fibrous material reacted with antibodies against type I and III collagen but not with those against laminin or type IV collagen by an indirect immunofluorescence technique. This case seemed to be a case of collagenofibrotic glomerulonephropathy.

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