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crescentic glomerulonephritis, a rare presentation of alport syndrome
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نویسنده
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ghasemi darbrood sholeh ,nili fatemeh ,salarvand samaneh ,malakoutian tahereh ,mehrazma mitra
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منبع
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iranian journal of pathology - 2022 - دوره : 17 - شماره : 4 - صفحه:496 -499
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چکیده
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Crescentic glomerulonephritis (gn) is a feature of severe glomerular injury. anti-gbm disease, immune-complex mediated glomerulonephritis, and anca-associated vasculitis are the main causes of crescentic gn. alport syndrome is a progressive form of hereditary nephritis presenting with hematuria and progression to proteinuria and renal failure. herein we present a 16-year-old male with rapidly progressive glomerulonephritis syndrome, sensory-neural hearing loss, and a family history of hematuria and proteinuria in his mother and aunt. light microscopic examination shows cellular crescent in glomeruli. in an electron microscopy study, gbm changes compatible with alport syndrome were identified. alport syndrome rarely can be presented as crescentic gn. electron microscopy is necessary for the diagnosis of this type of pauci-immune crescentic glomerulonephritis.
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کلیدواژه
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alport ,crescentic glomerulonephritis ,hereditary nephritis
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آدرس
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iran university of medical sciences, shahid hasheminejad kidney center, department of nephrology, iran, tehran university of medical sciences, imam khomeini hospital complex, department of pathology, iran, tehran university of medical sciences, imam khomeini hospital complex, department of pathology, iran, iran university of medical sciences, shahid hasheminejad kidney center, department of nephrology, iran, iran university of medical sciences, shahid hasheminejad kidney center, department of pathology, iran
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پست الکترونیکی
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mitmehr@yahoo.com
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Authors
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