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Paroxysmal Nocturnal Hemoglobinuria Presenting as Recurrent Jejunitis / 대한내과학회지
Korean Journal of Medicine ; : 132-135, 2016.
Article in Korean | WPRIM | ID: wpr-65771
ABSTRACT
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.
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Thrombosis / Bone Marrow / Hematopoietic Stem Cells / Diagnosis, Differential / Hemoglobinuria / Hemoglobinuria, Paroxysmal / Hemolysis / Ischemia Type of study: Diagnostic study Limits: Adult / Humans Language: Korean Journal: Korean Journal of Medicine Year: 2016 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Thrombosis / Bone Marrow / Hematopoietic Stem Cells / Diagnosis, Differential / Hemoglobinuria / Hemoglobinuria, Paroxysmal / Hemolysis / Ischemia Type of study: Diagnostic study Limits: Adult / Humans Language: Korean Journal: Korean Journal of Medicine Year: 2016 Type: Article