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KAWASAKI ATIPICO PDF

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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Universidad de los Andes, Santiago, Chile. Servicio de Urgencia CFC. Kawasaki disease KD is a serious disease in children due to its potential complications and sequelae if not promptly and adequately managed. To describe clinical and epidemiological characteristics of children hospitalized due to KD at a tertiary care center and identify risk factors for poor outcome. Retrospective and descriptive study of 32 medical records of patients hospitalized with diagnosis of KD at a tertiary care center of Santiago, Chile between February and May The annual frequency was of 5 cases, mainly boys and during spring.

The median age at diagnosis was 1. Coronary artery affection, including dilatation or aneurisms, occurred in All patients were treated with aspirin and intravenous immunoglobulin IVIG ; 4 patients required a second dose. No deaths were reported. The identified risk factors for poor outcome were age older than 5 years and hypoalbumin-emia. KD is an infrequent disease that mainly occurs in children younger than 5 years and with a typical presentation.

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There are risk factors associated with poor outcome. Kawasaki disease, coronary artery, immunoglobulin.

Medwave – Kawasaki atípico o incompleto

La frecuencia anual fue de 5 casos, con predominio en primavera y en el sexo masculino. Cuatro pacientes requirieron una segunda dosis de IGIV. Enfermedad de Kawasaki, arteria coronaria, inmunoglobulina.

Para los 32 pacientes estudiados se pueden observar en la Tabla 1.

En nuestra serie hubo claro predominio en primavera. La lengua se observa eritematosa, con papilas prominentes y eritema difuso que le da un aspecto “aframbuesado”.

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, los casos considerados graves no requirieron estos tratamientos.

Pese a la gravedad del cuadro, no fue administrada una segunda dosis de IGIV. En nuestra serie no se registraron muertes. Enfermedad de Kawasaki, Nelson. McGraw-Hill Interamericana ; p. Diagnosis, treatment, and long-term management of Kawasaki disease: Summary of the American Heart Association Guidelines ; Incident survey of Kawasaki disease in and in Japan.

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Diagnosis, treatment and outcome of Kawasaki disease in an Australian tertiary setting: A review of three year experience. J Paediatr Child Health ; Epidemiologic and clinical characteristics of Kawasaki disease in Chile.

Kawasaki atípico o incompleto – Semantic Scholar

kawaski Rev Chil Pediatr ; v. Intravenous immunoglobulin for the treatment of Kawasaki disease in children. Cochrane Database of Systematic Reviews. Epidemiologic picture of Kawasaki disease in Korea, Pediatrics Internat ; Kawasaki disease in New Zeland. J Pediatr Child Health ; v. Rev Chil Pediatr ; The riddle of Kawasaki disease. N Engl Med J ; 7: Clin Microbiol Rev ; 11 3: Prediction of intravenous immunoglobulin unresponsiveness in patients with Kawasaki disease.

Kawasaki disease in the older child.

An Pediatr Barc ; 73 1: Histocytic haemophagocytosis in a patient with Kawasaki disease: Eur J Pediatr ; Kawasaki disease followed by hemophagocytic syndrome.

Acta Pediatr ; Are children with Kawasaki disease and prolonged fever at risk for macrophage activation syndrome?

Enfermedad de Kawasaki. Revisión de la literatura

Hemophagocytosis complicating Kawasaki disease. Pediatr Hematol Oncol ; Rev Chil Pediatr ; 76 4: Isolda Budnik Ojeda isolbudnik gmail.

Rev Chil Infect ; 28 5:

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