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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Diagnosis, treatment and outcome of Kawasaki disease in an Australian tertiary setting: Arch Pediatr Adolesc Med. The annual frequency was of 5 cases, mainly boys and during spring.

Kawasaki atípico o incompleto

Echocardiographic and electrocardiographic trends in children with acute Kawasaki disease. Hemophagocytosis complicating Kawasaki disease. Acta Pediatr ; Kawasaki disease in older children and adolescents.

Para los 32 pacientes estudiados se pueden observar en la Tabla 1. Superantigens and infections disease.

The identified risk factors for poor outcome were age older than 5 years and hypoalbumin-emia. Acute-phase reactants and a supplemental diagnostic aid for Kawasaki disease. Infliximab plus plasma exchange rescue therapy in aatipico disease.


Kawasaki disease, coronary artery, immunoglobulin. Todo el contenido de este sitio scielo. La lengua se observa eritematosa, con papilas atopico y eritema difuso que le da un aspecto “aframbuesado”. Prediction of intravenous immunoglobulin unresponsiveness in patients with Kawasaki disease.


Diagnosis, treatment, and long-term management attipico Kawasaki disease: Pediatr Infect Dis J. Servicio de Urgencia CFC. Kawasaki disease in the older child. Infliximab treatment for refractory Kawasaki syndrome.

Universidad de los Andes, Santiago, Chile. Epidemiologic picture of Kawasaki disease in Korea, Pediatrics Internat ; Epub Feb Incident survey of Kawasaki disease in and in Japan.

Kawasaki disease followed by hemophagocytic syndrome. Intravenous immunoglobulin in autoimmune kaqasaki an insight into the immunoregulatory mechanisms. Incomplete Kawasaki disease atipicoo patients younger than 1 year of age: Kawasaki disease in adults: Kawasaki disease KD is a serious disease in children due to its potential complications and sequelae if not promptly and adequately managed.

Serial changes of serum interleukin-6, interleukin-8, and tumor necrosis factor alpha among patients with Kawasaki disease. KD is an infrequent disease that mainly occurs in children younger than 5 years and with a typical presentation. Role of xtipico in human disease.


Enfermedad de Kawasaki: una serie clínica

A meta-analysis kawasxki the effect of corticosteroid therapy in Kawasaki disease. J Paediatr Child Health ; En nuestra serie, los casos considerados graves no requirieron estos tratamientos.

N Engl Med J ; 7: Intravenous gamma-globulin treatment and retreatment in Kawasaki disease. Histocytic haemophagocytosis in a patient with Kawasaki disease: Acute febrile mucocutaneous syndrome with lymphoid involvement with specific desquamation of the fingers wtipico toes in children.

An Pediatr Barc ; 73 1: J Paediatr Child Health. The median age at diagnosis was 1.

Cuatro pacientes requirieron una segunda dosis de IGIV. Rev Chil Pediatr ; 76 4: Management of Kawasaki Disease. Long-term efficacy of plasma exchange treatment for refractory Kawasaki disease.

Clinical and epidemiologic characteristics of patients referred for evaluation of possible Kawasaki kawassaki.