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1.
Rev. argent. dermatol ; Rev. argent. dermatol;92(2)abr.-jun. 2011. ilus
Artigo em Espanhol | LILACS | ID: lil-634428

RESUMO

El trabajo aporta un nuevo caso de leucemia cutis, raro en frecuencia, que presenta un comienzo clínico muy poco habitual, a tener en cuenta. Fueron necesarias varias biopsias para llegar al diagnóstico de la paciente. La supervivencia de la paciente está por encima de la media en estos casos.


The work presents a new case of leukemia cutis, rare in frequency, which has a very unusual clinical onset to take into account. It took several biopsies for the diagnosis of the patient. The survival of the patient is above average in these cases.

4.
Bol Med Hosp Infant Mex ; 49(12): 832-8, 1992 Dec.
Artigo em Espanhol | MEDLINE | ID: mdl-1492913

RESUMO

IgA nephropathy, also called Berger's disease, is characterized by recurrent gross hematuria or persistent microscopic hematuria, together with mesangial glomerular deposits of IgA found in the renal biopsy. Seven children with IgA nephropathy were studied. Most of them presented initially with recurrent macroscopic hematuria and low or moderate-grade proteinuria, without hypertension or renal function impairment. Only one patient presented with a rapidly progressive glomerulonephritis. Four patients did not receive any treatment; one of them is in remission, one has improved and two remain with moderate proteinuria and hematuria. One patient with significant proteinuria improved after prednisone and azathioprine treatment. The patient with rapidly progressive glomerulonephritis improved his renal function after oral prednisone and intravenous boluses of methylprednisolone and cyclophosphamide.


Assuntos
Glomerulonefrite por IGA/diagnóstico , Adolescente , Biópsia , Criança , Pré-Escolar , Feminino , Hematúria/diagnóstico , Humanos , Rim/patologia , Masculino , Microscopia Eletrônica , Proteinúria/diagnóstico , Recidiva
5.
Bol Med Hosp Infant Mex ; 49(9): 600-4, 1992 Sep.
Artigo em Espanhol | MEDLINE | ID: mdl-1388785

RESUMO

Several renal and renal-related disturbances have been described in patients with AIDS (acquired immune deficiency syndrome), in adults and children as well. These are mainly electrolyte and acid-base imbalance, acute renal failure and nephrotic syndrome. The latter is usually steroid non-responder. The renal histopathological lesions described more commonly are minimal change, mesangial hyperplasia and focal segmental glomerulosclerosis. Herein, we describe a 5 year-old with AIDS, that developed nephrotic syndrome, characterized by edema, ascites, hypoalbuminemia and massive proteinuria. A percutaneous renal biopsy showed mesangial proliferation. She did not respond to a 6 week treatment with prednisone. She died with sepsis after several viral and bacterial infections.


Assuntos
Nefropatia Associada a AIDS , Síndrome Nefrótica , Pré-Escolar , Feminino , Humanos
6.
Bol Med Hosp Infant Mex ; 49(6): 388-90, 1992 Jun.
Artigo em Espanhol | MEDLINE | ID: mdl-1632913

RESUMO

Africanized bees are unique in their aggressive behavior, characterized by massive attacks during which the victims are injected an important amount of venom. For this reason, Africanized bees are extremely dangerous. Their venom contains biological toxic substances, mainly mellitin, phospholipases, histamine, hyaluronidase and apamin. Non-sensitized persons that survive a massive attack may develop acute renal failure, as a consequence of the severe hemolysis, rhabdomyolysis and shock. These complications may lead to acute renal tubular necrosis. Also, the clinical pattern and treatment of the acute renal failure secondary to bee stings are discussed.


Assuntos
Injúria Renal Aguda/etiologia , Abelhas , Mordeduras e Picadas de Insetos/complicações , Injúria Renal Aguda/diagnóstico , Injúria Renal Aguda/fisiopatologia , Injúria Renal Aguda/terapia , Animais , Venenos de Abelha/toxicidade , Humanos , Mordeduras e Picadas de Insetos/diagnóstico , Mordeduras e Picadas de Insetos/fisiopatologia , Mordeduras e Picadas de Insetos/terapia
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