The Apprentice Doctor

Aplastic crisis

Discussion in 'Case Studies' started by Essam Abdelhakim, Mar 11, 2025.

  1. Essam Abdelhakim

    Essam Abdelhakim Well-Known Member

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    A 5-year-old child with sickle cell disease presents with severe pallor, tachycardia, and lethargy. Blood tests show:

    • Hb: 4 g/dL (very low)
    • Reticulocyte count: Low
    What is the most likely cause?

    A) Splenic sequestration crisis
    B) Aplastic crisis
    C) Haemolytic crisis
    D) Iron deficiency anaemia
    E) Thalassaemia

    Correct Answer:

    B) Aplastic crisis

    Explanation:

    Aplastic crisis in sickle cell disease is caused by parvovirus B19 infection, leading to:

    • Severe anaemia (low Hb)
    • Low reticulocyte count (bone marrow suppression)
    • A) Splenic sequestration crisisIncorrect. Causes enlarged spleen + sudden drop in Hb, but reticulocyte count is high.
    • C) Haemolytic crisisIncorrect. Causes low Hb, but high reticulocytes (increased RBC destruction).
    • D) Iron deficiency anaemiaIncorrect. Unlikely in a child with sickle cell disease.
    • E) ThalassaemiaIncorrect. Chronic anaemia, not sudden crisis.
    Key Tips for PLAB 1:

    Severe anaemia + low reticulocytes = Aplastic crisis (parvovirus B19).
    Treatment = Blood transfusion, supportive care.
     

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