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Pancytopaenia

From Surgopaedia

Pancytopaenia - anaemia, thrombocytopaenia, neutropaenia

Bicytopaenia - anaemia with luekopaenia or thrombocytopaenia

Aetiology

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Acquired
    • Bone marrow infiltration/replacement
      • Malignant
        • Acute leukemias
        • Chronic leukemias/myeloproliferative neoplasms (MPN)
        • Myelodysplastic syndromes (MDS)
        • Multiple myeloma
        • Metastatic cancer
      • Non-malignant
        • Myelofibrosis
        • Infectious (eg, fungal, tuberculous)
        • Storage diseases
      • Bone marrow failure
        • Immune destruction/suppression
          • Aplastic anemia/paroxysmal nocturnal hemoglobinuria
          • Medications¶
            • Cytotoxic drugs
            • Idiosyncratic reactions to medications
          • Large granular lymphocyte leukemia
          • Autoimmune disorders (eg, systemic lupus erythematosus [SLE], rheumatoid arthritis [RA], sarcoidosis)
          • Hemophagocytic lymphohistiocytosis (HLH)
        • Nutritional
          • Megaloblastic (vitamin B12, folate)
          • Excessive alcohol
          • Other (eg, copper deficiency, zinc toxicity)
          • Malnutrition/anorexia nervosa with gelatinous degeneration
        • Marrow suppression
          • Viral infection (eg, HIV, hepatitis, Epstein-Barr virus [EBV])
        • Ineffective hematopoiesis (eg, MDS, nutritional)
    • Destruction/sequestration/redistribution
      • Consumption
        • Disseminated intravascular coagulation (eg, associated with sepsis, acute promyelocytic leukemia)
      • Splenomegaly
        • Portal hypertension/cirrhosis
        • Infections (eg, EBV)
        • Autoimmune disorders (eg, SLE, RA/Felty syndrome)
        • Malignancies (eg, lymphomas, MPN)
        • Myelofibrosis with myeloid metaplasia
        • Storage diseases (eg, Gaucher)
Congenital
    • Wiskott Aldrich syndrome
    • Fanconi anemia
    • Dyskeratosis congenital/telomere biology disorders
    • Shwachman-Diamond syndrome
    • GATA2 deficiency
    • Hemophagocytic lymphohistiocytosis (HLH)


Red flags

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  • Red flags
    • Severe pancytopaenia
    • Blasts or immature myeloid/lymphoid forms - acute leukaemia
    • Abnormal lymphocytes (hairy cells, large granular lymphocytes, prolymphocytes)
    • Leukoerythroblastosis with or without teardrop cells
    • Pancytopaenia with haemolysis or thrombosis
    • Pancytopaenia or bicytopaenia in an older individual with normal B12, folate and copper