Acute hepatitis as a prequel to very severe aplastic anemia

Author:

Weiler-Normann Christina1,Hartl Johannes1,Weidemann Sören2,von Pein Ute-Marie3,Fiedler Walter4,Schramm Christoph1,Brinkert Florian5,Kröger Nicolaus3,Christopeit Maximilian3

Affiliation:

1. I. Department of Medicine, University Medical Center of Hamburg-Eppendorf, Hamburg, Germany

2. Institute of Pathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany

3. Department of Stem Cell Transplantation, University Medical Center Hamburg-Eppendorf, Hamburg, Germany

4. II. Department of Medicine, University Medical-Center Hamburg-Eppendorf, Hamburg, Germany

5. Department of Pediatrics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany

Abstract

AbstractSevere aplastic anemia is a rare and potentially life-threatening disease of the bone marrow often requiring allogeneic hematopoietic stem cell transplantation. Pathogenesis of the disease can vary and often remains enigmatic. Occasionally, severe aplastic anemia is associated with prior severe acute hepatitis. Differential diagnosis of acute non-viral hepatitis challenges the physician as pathogenesis remains unclear.We here present a case of a young patient presenting with acute hepatitis followed by severe aplastic anemia successfully treated with allogeneic hematopoietic stem cell transplantation. Due to immunosuppressive treatment with azathioprine for acute hepatitis of putative autoimmune pathogenesis and coincident infection with parvovirus B19, diagnosis of the sequential disease of acute hepatitis followed by severe aplastic anemia was complicated. We discuss the caveats and present a review of the literature.

Publisher

Georg Thieme Verlag KG

Subject

Gastroenterology

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