What is the significance of leukopenia (White Blood Cell count of 4.1) with neutropenia (absolute neutrophil count of 1652) in a 15-year-old male?

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Last updated: May 14, 2025View editorial policy

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Differential Diagnosis for a 15-year-old Male with WBC of 4.1 and Absolute Neutrophils of 1652

  • Single Most Likely Diagnosis
    • Viral infection (e.g., upper respiratory tract infection): This is a common cause of mild leukopenia, especially in adolescents. The body's response to viral infections can temporarily suppress bone marrow production, leading to a decrease in white blood cell count.
  • Other Likely Diagnoses
    • Bone marrow suppression due to medication: Certain medications, such as chemotherapy agents or some antibiotics, can suppress bone marrow activity, leading to leukopenia.
    • Vitamin deficiencies (e.g., vitamin B12 or folate deficiency): Deficiencies in these vitamins can impair bone marrow function, resulting in decreased production of blood cells, including neutrophils.
    • Chronic infections (e.g., tuberculosis, HIV): Chronic infections can lead to bone marrow suppression and leukopenia.
  • Do Not Miss Diagnoses
    • Aplastic anemia: A rare but serious condition where the bone marrow fails to produce blood cells. It can be caused by various factors, including viral infections, exposure to toxins, or autoimmune disorders.
    • Leukemia or lymphoma: Although less common, these malignancies can present with leukopenia and require prompt diagnosis and treatment.
    • Severe combined immunodeficiency (SCID): A group of rare disorders caused by mutations in different genes involved in the development and function of the immune system, leading to severe immunodeficiency.
  • Rare Diagnoses
    • Congenital neutropenia: A rare genetic disorder characterized by an abnormally low number of neutrophils, which can increase the risk of recurrent infections.
    • Cyclic neutropenia: A rare disorder where neutrophil counts fluctuate periodically, often resulting in recurrent infections.
    • Shwachman-Diamond syndrome: A rare genetic disorder that affects the bone marrow, pancreas, and skeleton, leading to neutropenia and other complications.

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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