PDF | Antecedentes: La enfermedad de Kawasaki es una vasculitis sistémica de etiología desconocida. La modalidad atípica se define como aquella en la cual. Request PDF on ResearchGate | Abdomen agudo como manifestación inicial de enfermedad de Kawasaki incompleta y atípica: Caso clínico | La enfermedad. Request PDF on ResearchGate | On May 1, , Jacklyn Cristina Guzmán Montealegre and others published Enfermedad de Kawasaki.

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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 aatipica to KD at a tertiary care center and identify risk factors for poor outcome.

[Neurological manifestations in atypical Kawasaki disease].

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.

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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.

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

[Neurological manifestations in atypical Kawasaki disease].

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.

Enffermedad de Kawasaki, Nelson.

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Hemophagocytosis complicating Enferjedad disease. Pediatr Hematol Oncol ; Rev Chil Pediatr ; 76 4: Isolda Budnik Ojeda isolbudnik gmail. Rev Chil Infect ; 28 5: