What is the diagnosis based on this CBC showing microcytic hypochromic anemia?

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Interpretation of CBC: Microcytic Hypochromic Anemia

This CBC shows a classic pattern of iron deficiency anemia with microcytic hypochromic parameters (low MCV, MCH, and MCHC) and elevated RDW. 1

CBC Analysis:

  • Hemoglobin: 9.8 g/dL (decreased)
  • Hematocrit (PCV): 30.8% (decreased)
  • MCV: 71.6 fL (decreased, microcytic)
  • MCH: 23.0 pg (decreased, hypochromic)
  • MCHC: 32.1 g/dL (low normal)
  • RDW: 18.7% (markedly elevated)
  • WBC (TLC): 6.72 (normal)
  • RBC: 4.24 (relatively preserved)
  • Platelet count: 203 (normal)
  • MPV: 11.8 (normal)

Diagnostic Interpretation:

Primary Diagnosis: Iron Deficiency Anemia

The combination of:

  • Low hemoglobin (9.8 g/dL)
  • Microcytosis (MCV 71.6 fL)
  • Hypochromia (MCH 23.0 pg)
  • Markedly elevated RDW (18.7%)

This pattern strongly suggests iron deficiency anemia, which is the most common cause of microcytic hypochromic anemia worldwide (approximately 80% of all anemia cases) 2.

Differential Diagnosis:

  1. Iron Deficiency Anemia

    • Most likely diagnosis based on the markedly elevated RDW (18.7%)
    • RDW elevation is characteristic of iron deficiency and helps distinguish it from thalassemia 1
  2. Thalassemia

    • Possible but less likely due to the very high RDW
    • Thalassemia typically presents with normal RDW despite very low MCV 1
    • Would need hemoglobin electrophoresis to confirm/exclude
  3. Anemia of Chronic Disease

    • Less likely as a sole cause given the degree of microcytosis and hypochromia
    • Could be present as a comorbid condition
  4. Sideroblastic Anemia

    • Rare genetic disorders affecting heme synthesis 3
    • Would require bone marrow examination showing ring sideroblasts

Next Steps in Management:

  1. Confirm iron deficiency with:

    • Serum ferritin (most sensitive test; <15 μg/L confirms iron deficiency) 1
    • Transferrin saturation (low in iron deficiency)
    • Consider CRP to assess for inflammation which can elevate ferritin 1
  2. Investigate underlying cause of iron deficiency:

    • Gastrointestinal blood loss (most common in adults)
    • Menstrual blood loss (in premenopausal women)
    • Malabsorption (celiac disease, post-gastrectomy)
    • Dietary insufficiency (more common in infants, children, pregnant women)
  3. Treatment:

    • Oral iron supplementation: ferrous sulfate 200mg three times daily 1
    • Continue for 3 months after hemoglobin normalizes to replenish stores
    • Monitor response with repeat CBC in 2-4 weeks (expect hemoglobin rise of ≥1 g/dL)

Common Pitfalls to Avoid:

  • Failure to investigate the cause of iron deficiency, especially in adult men and postmenopausal women where GI bleeding must be excluded 1
  • Misinterpreting ferritin levels in the presence of inflammation (ferritin is an acute phase reactant) 1
  • Relying solely on MCV/MCH without confirming iron status with appropriate tests 1
  • Stopping iron therapy prematurely before replenishing iron stores (continue for 3 months after hemoglobin normalizes) 1

Special Considerations:

  • If oral iron is not tolerated or ineffective, consider IV iron therapy 1
  • In cases with severe anemia or hemodynamic compromise, blood transfusion may be necessary
  • For patients with persistent unexplained iron deficiency despite treatment, consider referral to a hematologist

References

Guideline

Diagnosis and Management of Anemia

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

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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