| Revista: | Annals of hepatology |
| Base de datos: | PERIÓDICA |
| Número de sistema: | 000419235 |
| ISSN: | 1665-2681 |
| Autores: | Chowdry, Shoket1 Rubin, Erin2 Sass, David A1 |
| Instituciones: | 1University of Pittsburgh, Department of Medicine, Pittsburgh, Pensilvania. Estados Unidos de América 2University of Pittsburgh, Department of Pathology, Pittsburgh, Pensilvania. Estados Unidos de América |
| Año: | 2012 |
| Periodo: | Jul-Ago |
| Volumen: | 11 |
| Número: | 4 |
| Paginación: | 559-563 |
| País: | México |
| Idioma: | Inglés |
| Tipo de documento: | Artículo |
| Enfoque: | Caso clínico, analítico |
| Resumen en inglés | Peripheral blood eosinophilia has been described in a broad variety of allergic, infectious, neoplastic and autoimmune diseases. To the best of our knowledge blood eosinophilia has never previously been reported in association with isolated autoimmune hepatitis (AIH) in the absence of other autoimmune conditions. Herein we report an interesting case of an 18 year old man who presented to our hospital with an acute autoimmune hepatitis diagnosed on the basis of clinical features, serology and histopathology. He was noted to have a moderate peripheral eosinophilia at diagnosis which resolved within days of initiation of corticosteroids for treatment of the AIH. Given the absence of other systemic conditions or drugs which may have produced the eosinophilia and its rapid resolution with treatment of the underlying liver disease, we wished to highlight this rather novel presentation of AIH |
| Disciplinas: | Medicina |
| Palabras clave: | Gastroenterología, Inmunología, Diagnóstico, Hepatitis autoinmune, Eosinofilia, Ictericia, Manifestaciones clínicas |
| Keyword: | Gastroenterology, Immunology, Diagnosis, Autoimmune hepatitis, Eosinophilia, Jaundice, Clinical manifestations |
| Texto completo: | Texto completo (Ver PDF) |
