Case Report : Pure red-cell aplasia and autoimmune hemolytic anemia in a patient with acute hepatitis A
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-yearold female with a diagnosis of AHA presented with severe anemia (hemog...
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Veröffentlicht in: | Clinical and molecular hepatology 2014-06, Vol.20 (2), p.204 |
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creator | Hyo Jeong Chang Dong Hyun Sinn Sung Gyun Cho Tae Hoon Oh Tae Joo Jeon Won Chang Shin Won Choong Choi |
description | 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-yearold 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. (Clin Mol Hepatol 2014;20:204-207) |
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We report herein a case of AHA complicated by both PRCA and AIHA. A 49-yearold 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. 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We report herein a case of AHA complicated by both PRCA and AIHA. A 49-yearold 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. 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We report herein a case of AHA complicated by both PRCA and AIHA. A 49-yearold 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. (Clin Mol Hepatol 2014;20:204-207)</abstract><pub>대한간학회</pub><tpages>4</tpages></addata></record> |
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subjects | Autoimmune hemolytic anemia Hepatitis A Pure red-cell aplasia |
title | Case Report : Pure red-cell aplasia and autoimmune hemolytic anemia in a patient with acute hepatitis A |
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