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1.
Maroc Medical. 1992; 14 (1-2): 48-53
em Francês | IMEMR | ID: emr-24773

RESUMO

Rosai Dorfman Disease is in most cases a benign, rare and ubiquitous entity. Its prime interest lies in the fact that it must be distinguished from other malign histiocytosis and neoplasms which simulate it on a clinical and/or histological level. The authors report one case with massive lymphadenopathy, anemia and other auto-immuns signs


Assuntos
Linfadenite/etiologia , Criança , Doenças Linfáticas
2.
Maroc Medical. 1990; 12 (3): 49-53
em Francês | IMEMR | ID: emr-17222

RESUMO

The authors report the case of a 13 years old girl affected by the progressive systemic scleroderma, complicated by the oesophagenal and renal affection revealed by a nephrotic syndrom. With the helf of litterature facts, we trying to discuss the prognostic value of the renal affection which exceptionnally happens over the scleroderma


Assuntos
Rim/patologia , Síndrome Nefrótica/diagnóstico , Criança
3.
Maroc Medical. 1990; 12 (3): 70-74
em Francês | IMEMR | ID: emr-17225

RESUMO

The authors report one case of a symmetrical gangrene of the feet noted during enteric fever in a 10 years old female child. Such complication is rare and it has a lot of pathogenic factors which all are incriminated in creating a low perfusion phenomenon occurring to a disseminated intravascular coagulation which is amplified or created by a blood circulation failure. A personal predisposition to this kind of complication is still hypothetic


Assuntos
Febre Tifoide/complicações , Criança
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