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1.
J Pediatr ; 138(4): 539-47, 2001 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-11295718

RESUMEN

OBJECTIVE: To assess the long-term systemic and neurologic responses to enzyme replacement therapy (ERT) with macrophage-targeted glucocerebrosidase in patients with type 3 Gaucher's disease. STUDY DESIGN: Patients with type 3 Gaucher's disease (n = 21), aged 8 months to 35 years, were enrolled in a prospective study. Enzyme dose was adjusted to control systemic manifestations. Clinical and laboratory evaluations were performed at baseline and every 6 to 12 months thereafter. Patients were followed up for 2 to 8 years. RESULTS: Significant improvement in hemoglobin levels, platelet count, and acid phosphatase values occurred. Liver and spleen volume markedly decreased, and bone structure improved. Nineteen patients had asymptomatic interstitial lung disease unresponsive to ERT. Supranuclear gaze palsy remained stable in 19 patients, worsened in one patient, and improved in one. Cognitive function remained unchanged or improved over time in 13 patients but decreased in 8 patients, 3 of whom developed progressive myoclonic encephalopathy accompanied by cranial magnetic resonance imaging and electroencephalographic deterioration. CONCLUSIONS: At relatively high doses, ERT reverses almost all the systemic manifestations in patients with type 3 Gaucher's disease. Most treated patients do not deteriorate neurologically. Novel therapeutic strategies are required to reverse the pulmonary and neuronopathic aspects of the disease.


Asunto(s)
Enfermedad de Gaucher/tratamiento farmacológico , Glucosilceramidasa/uso terapéutico , Adolescente , Adulto , Determinación de la Edad por el Esqueleto , Niño , Preescolar , Electroencefalografía/métodos , Femenino , Enfermedad de Gaucher/sangre , Enfermedad de Gaucher/diagnóstico , Enfermedad de Gaucher/psicología , Glucosilceramidasa/administración & dosificación , Humanos , Pruebas de Inteligencia , Imagen por Resonancia Magnética , Masculino , Tomografía Computarizada por Rayos X , Resultado del Tratamiento
2.
J Pediatr ; 126(4): 596-7, 1995 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-7699540

RESUMEN

Partial splenectomy was introduced to achieve the benefits of splenectomy and to avoid the risk of overwhelming infection in patients with symptomatic Gaucher disease. We observed regrowth of the splenic remnant, reemergence of preoperative symptoms, and new bone involvement among most of our patients who had undergone partial splenectomy. Enzyme replacement therapy has markedly limited indications for splenectomy, partial or total, for Gaucher disease.


Asunto(s)
Enfermedad de Gaucher/cirugía , Esplenectomía , Adolescente , Adulto , Enfermedades Óseas/etiología , Niño , Femenino , Estudios de Seguimiento , Enfermedad de Gaucher/fisiopatología , Humanos , Masculino , Persona de Mediana Edad , Osteonecrosis/etiología , Bazo/crecimiento & desarrollo , Resultado del Tratamiento
3.
J Pediatr ; 120(2 Pt 1): 277-80, 1992 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-1735829

RESUMEN

Long-term studies of a child with Gaucher disease indicated that the response to treatment with macrophage-targeted glucocerebrosidase (glucosylceramidase) is dose dependent, and that the hematologic response precedes the skeletal response.


Asunto(s)
Enfermedad de Gaucher/tratamiento farmacológico , Glucosilceramidasa/administración & dosificación , Abdomen/patología , Huesos/patología , Niño , Relación Dosis-Respuesta a Droga , Estudios de Seguimiento , Enfermedad de Gaucher/diagnóstico , Enfermedad de Gaucher/enzimología , Glucosilceramidasa/sangre , Humanos , Macrófagos/efectos de los fármacos , Imagen por Resonancia Magnética , Masculino
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