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[Neurological manifestations in atypical Kawasaki disease].
- Source :
-
Revista alergia Mexico (Tecamachalco, Puebla, Mexico : 1993) [Rev Alerg Mex] 2017 Jul-Sep; Vol. 64 (3), pp. 376-380. - Publication Year :
- 2017
-
Abstract
- Background: Kawasaki disease (KD) is a type of systemic vasculitis of unknown etiology. Atypical Kawasaki disease is defined as that where there are signs and symptoms not corresponding to the classical criteria for this nosological entity. Children with atypical Kawasaki disease may present with acute abdominal symptoms, meningeal irritation, pneumonia or renal failure.<br />Clinical Cases: We describe 4 children with ages ranging from 2 to 12 years who had atypical Kawasaki disease, with neurological and gastrointestinal symptoms as part of the systemic presentation of the disease. Treatment consisted of immunoglobulin and corticosteroids with good evolution.<br />Conclusions: KD is a systemic vasculitis that can involve many territories. Atypical manifestations can mislead the clinician and delay diagnosis. Pediatricians and sub-specialists should be aware of these neurological manifestations in order to provide adequate and opportune treatment.
- Subjects :
- Aspirin therapeutic use
Child
Child, Preschool
Diagnosis, Differential
Diarrhea etiology
Drug Therapy, Combination
Epilepsy, Tonic-Clonic diagnosis
Gallbladder Diseases etiology
Humans
Immunoglobulins, Intravenous therapeutic use
Immunosuppressive Agents therapeutic use
Male
Meningoencephalitis diagnosis
Mucocutaneous Lymph Node Syndrome drug therapy
Vomiting etiology
Epilepsy, Tonic-Clonic etiology
Mucocutaneous Lymph Node Syndrome complications
Subjects
Details
- Language :
- Spanish; Castilian
- ISSN :
- 0002-5151
- Volume :
- 64
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Revista alergia Mexico (Tecamachalco, Puebla, Mexico : 1993)
- Publication Type :
- Academic Journal
- Accession number :
- 29046034
- Full Text :
- https://doi.org/10.29262/ram.v64i3.231