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1.
J Pediatr ; 128(1): 149-51, 1996 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-8551408

RESUMEN

We performed percutaneous liver biopsy in nine children who had received a weekly dose of methotrexate, 10 mg/m2 per week, for at least 3 years to address the concern about subclinical liver toxicity from single, weekly, low-dose methotrexate therapy for juvenile rheumatoid arthritis. No patient had clinical or biochemical evidence of liver injury. All biopsy results were interpreted as normal. These results suggest that the recommendations of the American College of Rheumatology for adults receiving single weekly methotrexate therapy for rheumatoid arthritis can be extended to children.


Asunto(s)
Artritis Juvenil/tratamiento farmacológico , Hígado/efectos de los fármacos , Metotrexato/efectos adversos , Adolescente , Biopsia con Aguja , Niño , Femenino , Humanos , Hígado/patología , Metotrexato/administración & dosificación , Factores de Tiempo
2.
J Pediatr ; 121(6): 937-40, 1992 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-1447662

RESUMEN

Three patients with nonpulmonary sarcoidosis had chronic erythema nodosum within the first 2 years of life. Each subsequently had renal sarcoidosis and nephrocalcinosis; hypercalcemia was documented in each patient and hypercalciuria in two patients. Treatment with prednisone was not uniformly successful in normalizing creatinine clearance. Nephrocalcinosis may be more common than previously reported in patients with sarcoidosis.


Asunto(s)
Nefrocalcinosis/etiología , Sarcoidosis/complicaciones , Biopsia , Calcitriol/sangre , Calcio/análisis , Niño , Enfermedad Crónica , Creatinina/sangre , Eritema Nudoso/etiología , Eritema Nudoso/metabolismo , Eritema Nudoso/patología , Humanos , Riñón/patología , Nefrocalcinosis/metabolismo , Nefrocalcinosis/patología , Sarcoidosis/metabolismo , Sarcoidosis/patología
3.
J Pediatr ; 121(5 Pt 1): 689-94, 1992 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-1432415

RESUMEN

From 1974 through 1991, a total of 583 children with Kawasaki disease were seen at the Hospital for Sick Children, in Toronto, of whom 80 (13.7%) had coronary artery involvement. There were 55 boys and 25 girls, whose mean age at onset was 2.9 +/- 2.5 years, followed for a mean period of 4.0 +/- 3.6 years. Giant aneurysms (maximum diameter > or = 8 mm) were found in 22 children, moderate-sized aneurysms (> or = 4 to < 8 mm) in 44, and dilation lesions (< 4 mm) in 14. Myocardial infarction occurred in 9 (1.5%), all of whom had giant aneurysms. The persistence rate for aneurysms was 72% at 1 year and 41% at 5 years of follow-up. In multivariate analysis, the regression of an aneurysm was significantly related to the severity of coronary artery lesions, initial treatment, and gender. Although > 80% of small or moderate-sized aneurysms regressed within 5 years, giant aneurysms did not regress during the follow-up period. In patients who received immune globulin therapy, coronary lesions tended to resolve more rapidly than in those treated with salicylate therapy alone, because 91% of the lesions in the former were small or moderate. These findings suggest that the severity of coronary artery involvement during the initial stages of Kawasaki disease influences the regression of these lesions, and that immune globulin treatment may improve outcome by reducing the incidence of severe lesions.


Asunto(s)
Aneurisma Coronario/complicaciones , Síndrome Mucocutáneo Linfonodular/complicaciones , Adolescente , Niño , Preescolar , Aneurisma Coronario/etiología , Aneurisma Coronario/cirugía , Femenino , Estudios de Seguimiento , Humanos , Inmunoglobulinas Intravenosas/uso terapéutico , Lactante , Masculino , Síndrome Mucocutáneo Linfonodular/terapia , Infarto del Miocardio/etiología , Pronóstico , Salicilatos/uso terapéutico
11.
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