Hematoma subcapsular esplénico en paciente portador de rasgo falciforme / Sub capsular splenic hematoma in a sickle cell trait carrier. Case report
Rev. méd. Chile
; 139(9): 1192-1195, set. 2011. ilus
Article
em Es
| LILACS
| ID: lil-612244
Biblioteca responsável:
BR1.1
ABSTRACT
Drepanocytic anemia is an uncommon hereditary disease in Chile. The heterozygous state of drepanocytic anemia or "sickle trait" has a frequency of 8 percent 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-year-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.
Palavras-chave
Texto completo:
1
Base de dados:
LILACS
Assunto principal:
Traço Falciforme
/
Esplenopatias
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Altitude
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Doença da Altitude
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Hematoma
Tipo de estudo:
Etiology_studies
Limite:
Humans
/
Male
Idioma:
Es
Ano de publicação:
2011
Tipo de documento:
Article