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Clinical and Molecular Hepatology ; : 204-207, 2014.
Article in English | WPRIM | ID: wpr-119483

ABSTRACT

Pure red cell aplasia (PRCA) and autoimmune hemolytic anemia (AIHA) have rarely been reported as an extrahepatic manifestation of acute hepatitis A (AHA). We report herein a case of AHA complicated by both PRCA and AIHA. A 49-year-old female with a diagnosis of AHA presented with severe anemia (hemoglobin level, 6.9 g/dL) during her clinical course. A diagnostic workup revealed AIHA and PRCA as the cause of the anemia. The patient was treated with an initial transfusion and corticosteroid therapy. Her anemia and liver function test were completely recovered by 9 months after the initial presentation. We review the clinical features and therapeutic strategies for this rare case of extrahepatic manifestation of AHA.


Subject(s)
Adult , Female , Humans , Male , Middle Aged , Young Adult , Acute Disease , Anemia, Hemolytic, Autoimmune/complications , Antineoplastic Agents, Hormonal/therapeutic use , Bone Marrow/pathology , Hepatitis A/complications , Prednisolone/therapeutic use , Red-Cell Aplasia, Pure/complications , Treatment Outcome
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