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Acta Paediatr Scand ; 79(6-7): 630-6, 1990.
Artigo em Inglês | MEDLINE | ID: mdl-2386054

RESUMO

We have investigated 65 children with isolated hematuria persisting for at least a year. Renal biopsy specimens were studied by light microscopy, electron microscopy and immunofluorescence with antisera specific against basement membrane components. The majority of the biopsies (62/65) showed variable histologic abnormalities. Four categories could be distinguished on combined histological and clinical criteria: Alport syndrome (n = 8), benign hematuria (n = 33, familial in 23), IgA nephropathy (n = 16) and increase in mesangial cells and matrix (n = 5). On the basis of our results, we suggest that a renal biopsy can establish diagnosis and prognosis in those children with isolated hematuria where the family history is negative. If the family has adult male individuals with isolated hematuria, a biopsy can usually be avoided, since this family history effectively excludes Alport syndrome. The use of antisera against basement membrane components did not allow a differentiation between Alport syndrome and benign hematuria. Goodpasture serum immunofluorescence was variable in the former and normally present in the latter.


Assuntos
Hematúria/patologia , Glomérulos Renais/patologia , Nefrite Hereditária/patologia , Membrana Basal/patologia , Biópsia , Criança , Pré-Escolar , Diagnóstico Diferencial , Feminino , Hematúria/genética , Humanos , Masculino , Microscopia Eletrônica , Microscopia de Fluorescência , Nefrite Hereditária/genética , Linhagem
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