| dc.contributor | | es-ES |
| dc.creator | Ugalde, Diego; Servicio de Hematología, Departamento de Medicina Interna, Hospital Clínico Universidad de ChileEstudiante de Medicina. Universidad de Chile | |
| dc.creator | Conte, Guillermo; Servicio de Hematología, Departamento de Medicina Interna, Hospital Clínico Universidad de Chile | |
| dc.creator | Ugalde, Héctor; Departamento Cardiovascular, Hospital Clínico Universidad de Chile | |
| dc.creator | Figueroa, Gastón; Servicio de Hematología, Departamento de Medicina Interna, Hospital Clínico Universidad de Chile | |
| dc.creator | Cuneo, Marianela; Servicio de Hematología, Departamento de Medicina Interna, Hospital Clínico Universidad de ChileTecnólogo Médico | |
| dc.creator | Muñoz, Macarena; Servicio de Hematología, Departamento de Medicina Interna, Hospital Clínico Universidad de ChileEstudiante de Medicina. Universidad de Chile. | |
| dc.creator | Mayor, Javiera; Servicio de Hematología, Departamento de Medicina Interna, Hospital Clínico Universidad de ChileEstudiante de Medicina. Universidad de Chile. | |
| dc.date | 2011-08-30 | |
| dc.date.accessioned | 2019-11-11T18:27:09Z | |
| dc.date.available | 2019-11-11T18:27:09Z | |
| dc.identifier | http://www.revistamedicadechile.cl/ojs/index.php/rmedica/article/view/1270 | |
| dc.identifier.uri | https://revistaschilenas.uchile.cl/handle/2250/110997 | |
| dc.description | Drepanocytic anemia is an uncommon hereditary disease in Chile. The heterozygous state of drepanocytic anemia or “sickle trait” has a frequency of 8% among Afro-Americans. A small number of patients carrying hemoglobin S are homozygous, with clinical manifestations of hemolytic anemia and thrombotic disease. Sickle trait is usually asymptomatic. We report a 59 years old male who presented an acute abdominal pain and dyspnea while staying at high altitude. Six days later, an angio CAT scan showed the presence of a subcapsular splenic hematoma that was managed conservatively. Sickle cell induction with sodium metabisulphite was positive. Hemoglobin electrophoresis confirmed the sickle trait. | es-ES |
| dc.language | es | |
| dc.publisher | Revista Médica de Chile | es-ES |
| dc.relation | http://www.revistamedicadechile.cl/ojs/index.php/rmedica/article/downloadSuppFile/1270/1672 | |
| dc.relation | http://www.revistamedicadechile.cl/ojs/index.php/rmedica/article/downloadSuppFile/1270/3372 | |
| dc.relation | http://www.revistamedicadechile.cl/ojs/index.php/rmedica/article/downloadSuppFile/1270/3373 | |
| dc.relation | http://www.revistamedicadechile.cl/ojs/index.php/rmedica/article/downloadSuppFile/1270/3374 | |
| dc.relation | http://www.revistamedicadechile.cl/ojs/index.php/rmedica/article/downloadSuppFile/1270/3375 | |
| dc.relation | http://www.revistamedicadechile.cl/ojs/index.php/rmedica/article/downloadSuppFile/1270/3376 | |
| dc.relation | http://www.revistamedicadechile.cl/ojs/index.php/rmedica/article/downloadSuppFile/1270/3377 | |
| dc.source | Revista Médica de Chile; Vol. 139, núm. 9 (2011): SEPTIEMBRE 2011 | es-ES |
| dc.source | 0034-9887 | |
| dc.subject | Altitude sickness; Sickle cell trait: Splenic rupture | es-ES |
| dc.title | Hematoma subcapsular esplénico en paciente portador de rasgo falciforme. | es-ES |
| dc.type | info:eu-repo/semantics/article | |
| dc.type | info:eu-repo/semantics/publishedVersion | |
| dc.type | | es-ES |
