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Updated: Jul 16 2017

Aplastic Anemia

Snapshot
  • A 5-year-old boy with sickle cell anemia presents to the emergency room with a low-grade fever, malaise, and a rash on his cheeks. On physical exam, his cheeks have a “slapped” appearance. His blood tests show Hb of 4.0 g/dL; MCV 90 fl; and 1% reticulocyte count. A bone marrow biopsy is obtained, showing hypocellularity and increased adipose tissue.
Introduction

  • Pancytopenia caused by diminished, absent, or destructed hematopoietic stem cells
  • With bone marrow aplasia
  • Epidemiology
    • no racial or gender predisposition
  • Multiple different causes
    • radiation
    • drugs (benzene, chloramphenicol, anti-epileptics, and alcohol)
    • insecticides
    • viruses (parvovirus B19, EBV, HIV, CMV, and HCV)
    • Fanconi anemia (congenital)
      • DNA repair defect
    • idiopathic
    • B12 and folate deficiency
    • PNH
    • SLE
    • PTU and methimazole
  • Commonly seen in sickle cell patients who are infected with parvovirus B19
Presentation
  • Symptoms/physical exam
    • insidious onset, but often initial symptoms are due to anemia or bleeding
    • (often normocytic) anemia
      • fatigue
      • malaise
      • pallor
    • thrombocytopenia
      • mucosal bleeding
      • petechiae
    • leukopenia
      • infections
Evaluation
  • Diagnosis of exclusion
  • Labs
    • anemia
    • leukopenia
    • thrombocytopenia
    • ↓ reticulocyte count
      • helps identify aplastic anemia in sickle cell patients, who usually have high baseline reticulocyte count
  • Most accurate test
    • bone marrow biopsy
      • normal cell morphology
      • hypocellular bone marrow with fatty infiltration
Differential Diagnosis
  • PNH
  • Myelodysplastic syndrome 
    • pancytopenia
    • increased MCV
    • low reticulocyte count
    • macroovalocytes
    • Pelger-Huet cells 
  • Infection
Treatment
  • Withdrawal causative agent if applicable
  • Supportive therapy
    • RBC transfusion
      • leukoreduced
    • platelet transfusion
  • Curative - bone marrow transplant for healthy patients under 50
  • Medical therapy – immunosuppressive agents for over 50 or those with comorbidities
    • antithymocyte globulin plus cyclosporine
  • Medical therapy – hematopoietic growth factors
    • G-CSF (filgastrim)
    • GM-CSF
Prognosis, Prevention, and Complications
  • Prognosis
    • 10-year survival rate
      • immunosuppression – 68%
      • stem cell transplant – 73%
  • Complications
    • infection
    • bleeding
    • complications of stem cell transplant
      • graft versus host disease
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