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Neutropenia

Quiz by Sadeq K. Ali Al-Salait

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12 questions
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  • Q1

    Which factor must be considered in defining neutropenia in African-American populations?

    Lower normal ANC range (1.0–1.5 × 10⁹/L)

    Highet baseline ANC.

    Reduced neutrophil function

    Frequent congenital mutations in neutrophil maturation

    Increased risk of autoimmune neutropenia

    30s
  • Q2

    Which is the most common cause of neutropenia in ambulatory adult patients?

    Bone marrow failure syndromes

    Drug-induced neutropenia

    Congenital neutropenia

    Autoimmune disorders

    Viral infections

    30s
  • Q3

    Which of the following is NOT a common cause of neutropenia in neonates?

    Congenital neutropenia

    Autoimmune maternal antibody transfer

    Maternal hypertension

    Infection

    Maternal iron deficiency

    30s
  • Q4

    Which molecular pathway is disrupted in Kostmann syndrome?

    ELA2

    LYST gene

    JAK/STAT pathway

    Fas-mediated apoptosis 

    30s
  • Q5

    What is the primary defect in Chediak-Higashi syndrome?

    Defective lysosomal trafficking

    Hyperactivation of NK cells

    Overexpression of CXCR4

    Phagocytic dysfunction

    Increased neutrophil lifespan

    30s
  • Q6

    Which bone marrow finding is characteristic of severe congenital neutropenia?

    Abnormal granulation of granulocyte precursors

    Maturation arrest at the promyelocyte stage

    Marked eosinophilia

    Absence of early precursors of granulocytes

    Hypercellularity with erythroid predominance

    30s
  • Q7

    What is the most common infectious complication in severe neutropenia?

    Tuberculosis 

    Meningitis

    Gastrointestinal candidiasis

    Bacterial sepsis, often gram-negative bacteremia

    Viral pneumonia

    30s
  • Q8

    Which neutropenia-associated condition has the highest risk of transformation to myelodysplastic syndrome (MDS) or acute myeloid leukemia (AML)?

    Kostmann syndrome

    Drug-induced neutropenia

    Viral-induced neutropenia

    Cyclic neutropenia

    Autoimmune neutropenia

    30s
  • Q9

    A 35-year-old male presents with fever (39.5°C), rigors, and fatigue. CBC shows WBC: 1.2 × 10⁹/L, ANC: 0.3 × 10⁹/L, hemoglobin: 11.5 g/dL, platelets: 250 × 10⁹/L. He has been on methimazole for Graves’ disease for 3 weeks. What is the most appropriate next step?

    Continue methimazole and monitor ANC

    Discontinue methimazole immediately and start broad-spectrum IV antibiotics

    Perform bone marrow biopsy urgently

    Start G-CSF and observe

    Prescribe antiviral therapy

    30s
  • Q10

    A 24-year-old female with a history of recurrent bacterial infections presents with neutropenia (ANC: 0.9 × 10⁹/L). She reports episodes of oral ulcers and fevers every 3 weeks since childhood. Her bone marrow biopsy shows normal cellularity. What is the most likely diagnosis?

    Benign ethnic neutropenia

    Cyclic neutropenia

    Autoimmune neutropenia

    Drug-induced agranulocytosis

    Myelodysplastic syndrome

    30s
  • Q11

    A 60-year-old male with chronic lymphocytic leukemia (CLL) on ibrutinib presents with ANC 0.7 × 10⁹/L and no active infection. He has mild fatigue but no fever. What is the most appropriate management?

    Perform a bone marrow biopsy immediately

    Discontinue ibrutinib permanently

    Start prophylactic G-CSF

    Monitor ANC closely and continue ibrutinib unless ANC drops <0.5 × 10⁹/L

    Start empiric antibiotics

    30s
  • Q12

    A 3-year-old boy presents with recurrent ear infections but no serious bacterial infections. His ANC is 0.5 × 10⁹/L. Anti-neutrophil antibodies are positive. Bone marrow biopsy shows normal myeloid maturation. What is the best initial treatment approach?

    G-CSF

    Bone marrow transplantation

    IVIG therapy

    Observation, as most cases resolve spontaneously

    Immediate IV antibiotics

    30s

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