[Association of Wilms' tumor, pseudohermaphroditism and glomerular nephropathy. Partial and complete forms of the syndrome]. / Asociación de tumor de Wilms, pseudohermafroditismo y nefropatía glomerular. Formas incompletas y completa del síndrome.
Bol Med Hosp Infant Mex
; 36(6): 1203-12, 1979.
Article
em Es
| MEDLINE
| ID: mdl-226110
ABSTRACT
Four patients, followed at the Buenos Aires Cildren's Hospital are reported one with a nephrotic syndrome and male pseudohermaphroditism, the second with nephrotic syndrome, male pseudohermaphroditism and Wilms' tumor, the third with pseudohermaphroditism and Wilms' tumor and the fourth with a nephrotic syndrome and Wilms' tumor. The cases presenting nephrotic syndrome, all had an early onset and a rapid and fatal course leading to death in renal failure or secondary to a related bacterial infection. The renal histology in all of the cases with nephrotic syndrome, was very similar diffuse involvement of all glomeruli consisting in a severe increase of the mesangial matrix, with scarce mesengial proliferation.
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Coleções:
01-internacional
Base de dados:
MEDLINE
Tipo de estudo:
Risk_factors_studies
Limite:
Adult
/
Child, preschool
/
Female
/
Humans
/
Infant
/
Male
Idioma:
Es
Ano de publicação:
1979
Tipo de documento:
Article