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Korean Journal of Medicine ; : 132-135, 2016.
Artigo em Coreano | WPRIM | ID: wpr-65771

RESUMO

Paroxysmal nocturnal hemoglobinuria (PNH) is a rare acquired hematopoietic stem cell disorder characterized by chronic complement-mediated intravascular hemolysis, nocturnal hemoglobinuria, predisposition to thrombosis and secondary bone marrow failure. Small bowel ischemia is a complication of PNH but has not been reported to date in a Korean adult. We report here a case of PNH presenting as recurrent jejunitis. Despite the uncommon etiology, PNH should be considered in the differential diagnosis of patients with unexplained recurrent jejunitis.


Assuntos
Adulto , Humanos , Medula Óssea , Diagnóstico Diferencial , Células-Tronco Hematopoéticas , Hemoglobinúria , Hemoglobinúria Paroxística , Hemólise , Isquemia , Trombose
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