1. Alport's Hereditary Nephritis with the Nephrotic Syndrome
- Author
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Kaname Okada, Masuhide Miyao, Shoyoji Kagami, Koichiro Kawakami, Ichioka T, Tatsuo Shimokawa, and Ichiro Yano
- Subjects
medicine.medical_specialty ,Pathology ,Kidney ,medicine.diagnostic_test ,urogenital system ,business.industry ,Glomerular basement membrane ,urologic and male genital diseases ,medicine.disease ,medicine.anatomical_structure ,Endocrinology ,Mesangium ,Internal medicine ,Pediatrics, Perinatology and Child Health ,Intramembranous ossification ,Biopsy ,medicine ,Renal biopsy ,business ,Nephrotic syndrome ,Nephritis - Abstract
Histopathological changes were studied in renal biopsy specimens from a ten-year-old boy diagnosed as having Alport's hereditary nephritis with the nephrotic syndrome. Biopsy specimens of the kidney showed mild hypercellularity with an increase of mesangial matrix, irregular thickening of the capillary walls in the glomeruli, and numerous clusters of interstitial foam cells by light microscopy. Granular deposits of IgG, IgM, C3 and fibrinogen were seen along the capillaries and partially in the mesangium by immunofluoroscopy. Ultrastructurally, the lesions had various abnormalities of the glomerular basement membrane, including splitting, thinning, disruption, reticulation and irregular thickening. The mesangial matrix was increased and intramembranous deposits were observed. Foam cells were seen among both tubular and interstitial cells.
- Published
- 1980
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