ENFERMEDAD DE KAWASAKI ATIPICA PDF

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

Manifestaciones neurológicas en la enfermedad de Kawasaki atípica

Pediatrics Internat ; Kawasaki disease in New Zeland. 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 Incident survey of Kawasaki disease in and in Japan.

Rev Chil Pediatr ; En nuestra serie hubo claro predominio en primavera. Diagnosis, treatment, and long-term management of Kawasaki disease: McGraw-Hill Interamericana ; p. La lengua se observa eritematosa, con papilas prominentes y eritema difuso que le da un aspecto “aframbuesado”. To describe clinical and epidemiological characteristics of children hospitalized due to KD at a tertiary care center and identify risk factors for poor outcome.

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Cochrane Database of Systematic Reviews. The identified risk factors for poor outcome were age older than 5 years and hypoalbumin-emia. Prediction of intravenous immunoglobulin unresponsiveness in patients with Kawasaki disease.

[Neurological manifestations in atypical Kawasaki disease].

The riddle of Kawasaki disease. There are risk factors associated with poor outcome. All patients were treated with aspirin and intravenous immunoglobulin IVIG ; 4 patients required a second dose. N Engl Med J ; 7: Diagnosis, treatment and outcome of Kawasaki disease in an Australian enfermead setting: Eur J Pediatr ; Cuatro pacientes requirieron una segunda dosis de IGIV.

An Pediatr Barc ; 73 1: En nuestra serie, los casos considerados graves no requirieron estos tratamientos.

[Neurological manifestations in atypical Kawasaki disease].

No deaths were reported. Kawasaki disease KD is a serious disease in children due to its potential complications and sequelae if not promptly and adequately managed. Are children with Kawasaki disease and prolonged fever at risk for macrophage activation syndrome?

Kawasaki disease, coronary artery, immunoglobulin. KD is an infrequent disease that mainly occurs in children younger than 5 years and with a typical presentation.

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Histocytic haemophagocytosis in a patient with Kawasaki disease: Rev Chil Pediatr ; v. Intravenous immunoglobulin for the treatment of Kawasaki disease in children.

Hemophagocytosis complicating Kawasaki disease. Enfermedad de Kawasaki, Nelson. Para los 32 pacientes estudiados se pueden observar en la Tabla 1.

The annual frequency was of 5 cases, mainly boys and during spring. Coronary artery affection, including dilatation or aneurisms, occurred in A review of three year experience. J Paediatr Child Health ; Clin Microbiol Rev ; 11 3: Rev Chil Pediatr ; 76 4: