Kawasaki atípico o incompleto. Citation data: Medwave, ISSN: , Vol: 9, Issue: Publication Year: Usage Full Text Views Kawasaki disease (KD, previously called mucocutaneous lymph node syndrome) is one of the most common vasculitides of childhood [1]. La enfermedad de Kawasaki (EK) es una vasculitis sistémica de la infancia, que Los casos se clasificaron según su forma de presentación, en típico, atípico e.

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The riddle of Kawasaki disease. Effects of statin therapy in children complicated with coronary arterial atipic late after Kawasaki disease: J Pediatr Child Health ; v. There are risk factors associated with poor outcome.

Epub Feb Incident survey of Kawasaki disease in and in Japan. Infliximab treatment for refractory Kawasaki syndrome. Kawasaki disease in New Zeland.

Kawasaki atípico o incompleto – Semantic Scholar

McGraw-Hill Interamericana ; p. Coagulopathy and platelet activation in Kawasaki syndrome: Prediction of intravenous immunoglobulin unresponsiveness atpico patients with Kawasaki disease. Para los 32 pacientes estudiados se pueden observar en la Tabla 1. Rev Chil Pediatr ; En casos no complicados, se recomienda repetir el ecocardiograma a las dos semanas y luego entre las seis y ocho semanas del inicio de la enfermedad 2. En nuestra serie no se registraron muertes. Clinical and epidemiologic characteristics of patients referred for evaluation of possible Kawasaki disease.

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Enfermedad de Kawasaki. Revisión de la literatura

Kawasaki syndrome and risk factors for coronary artery abnormalities, United States Clin Microbiol Rev ; 11 3: Diagnosis, treatment, and long-term management of Kawasaki disease: Role of superantigens in human disease. Prediction of intravenous immunoglobulin unresponsiveness in patients with Kawasaki disease. Complete and incomplete Kawasaki disease: The identified risk factors for poor outcome were age older than 5 years and hypoalbumin-emia.

Pediatr Infect Dis J. La frecuencia anual fue de 5 casos, con predominio en primavera y en el sexo masculino.

The median age at diagnosis was 1. KD is an infrequent disease that mainly occurs in children younger than 5 years and with a typical presentation. Acute febrile mucocutaneous syndrome with lymphoid involvement with specific mawasaki of the fingers and toes in children.

Kawasaki atípico o incompleto

Prediction of resistance to intravenous immunoglobulin treatment in patients with Kawasaki disease. Failure to diagnose Kawasaki disease at the extremes of the pediatric age range.

Rev Chil Pediatr ; v. Pese a la gravedad del cuadro, no fue administrada una segunda dosis de IGIV. Kawasaki disease followed by hemophagocytic syndrome. Management of Kawasaki Disease.


The differentiation of kaawasaki Kawasaki disease, atypical Kawasaki disease, and acute adenoviral infection: Acta Pediatr ; An Pediatr Barc ; 73 1: Cuatro pacientes requirieron una segunda dosis de IGIV. Eur J Pediatr ; All patients were treated with aspirin and intravenous immunoglobulin IVIG ; 4 patients required a second dose.

Intravenous gamma-globulin treatment and retreatment in Kawasaki disease. Update on etio and immunopathogenesis of Kawasaki disease.

To describe clinical and epidemiological characteristics of children hospitalized due to KD at a tertiary care center and identify risk factors for poor outcome. Hemophagocytosis complicating Kawasaki disease. Histocytic haemophagocytosis in a patient with Kawasaki disease: Atipivo of non-responsiveness to standard high-dose gamma-globulin therapy in patients with acute Kawasaki disease before starting initial treatment.

Cochrane Database of Systematic Reviews. Pediatr Hematol Oncol ; Corticosteroid pulse combination therapy for refractory Kawasaki disease: La lengua se observa eritematosa, con papilas prominentes y atupico difuso que le da un aspecto “aframbuesado”.

Long-term efficacy of plasma exchange treatment for refractory Kawasaki disease.

Kawasaki disease in adults: Infliximab plus plasma exchange rescue therapy in kawasaki disease.