| Journal: | Revista médica del Hospital General de México |
| Database: | PERIÓDICA |
| System number: | 000439525 |
| ISSN: | 0185-1063 |
| Authors: | Díaz García, Juan D1 Carrera Patiño, Fabián A1 |
| Institutions: | 1Hospital General Dr. Manuel Gea González, División de Medicina Interna, Ciudad de México. México |
| Year: | 2020 |
| Season: | Ene-Mar |
| Volumen: | 83 |
| Number: | 2 |
| Pages: | 66-69 |
| Country: | México |
| Language: | Inglés |
| Document type: | Artículo |
| Approach: | Analítico, descriptivo |
| English abstract | Evans syndrome is a very rare disorder in medical practice that can be both idiopathic and secondary to another underlying pathology. It is a clinical manifestation of autoimmune hemolytic anemia (AIHA) that can be simultaneous or subsequent to autoimmune thrombocytopenia (AITP). Sometimes, it can be accompanied by autoimmune neutropenia. It is estimated that 0.8-4% of patients with ITP or AIHA suffer from this syndrome. The case of a 32-year-old female patient with a history of systemic lupus erythematosus is described, who was admitted at the emergency unit of our hospital, presenting symptoms of asthenia, adynamia, and hyporexia |
| Disciplines: | Medicina |
| Keyword: | Hematología, Inmunología, Síndrome de Evans, Anemia hemolítica autoinmune, Trombocitopenia autoinmune, Lupus eritematoso sistémico |
| Keyword: | Hematology, Immunology, Evans syndrome, Autoimmune hemolytic anemia, Autoimmune thrombocytopenia, Systemic lupus erythematosus |
| Full text: | https://www.hospitalgeneral.mx/frame_esp.php?id=59 |
