alexa Incompatible Blood Transfusion In Autoimmune Hemolytic Anemia In An Adult Asymptomatic Hepatitis B Carrier: A Case Report | 64915
ISSN: 2155-9864

Journal of Blood Disorders & Transfusion
Open Access

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7th World Hematologists Congress
May 08-09, 2017 Barcelona, Spain

Rizza T Antenor
Southern Philippines Medical Center, Philippines
Posters & Accepted Abstracts: J Blood Disord Transfus
DOI: 10.4172/2155-9864-C1-023
Abstract
Autoimmune hemolytic anemia is an uncommon condition caused by antibodies directed against red blood cells causing their premature destruction. Clinical manifestations include anemia, jaundice, splenomegaly, reticulocytosis, elevated serum bilirubin, and positive direct antiglobulin test. Autoimmune hemolytic anemia (AIHA) can either be idiopathic or secondary to an underlying disease process. Infection accounts for 5% of cases of secondary AIHA. AIHA in asymptomatic hepatitis B carrier is rare with only two cases reported worldwide. Both cases were pediatric patients. We presented with a case of a 27 year old male who came in due to anemia. Patient presented with the classic manifestation of AIHA and workup for underlying cause revealed a carrier state of hepatitis B infection. Patient was unresponsive to steroid and was persistently dyspneic and tachycardic. Blood transfusion with an incompatible blood was done which resolved the patient’s symptoms. Steroid remains to be the mainstay of treatment for AIHA. However, blood transfusion may be beneficial to symptomatic patients at risk for complications of severe anemia. Although sustained remission is typical in inactive carriers of hepatitis B, reactivation remains a possibility, hence, patient education and good follow up is essential.
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