What is the diagnosis and recommended management for a patient with mild iron deficiency, normal hemoglobin and hematocrit, and negative autoimmune antibody panel?

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Diagnosis: Early Iron Deficiency Without Anemia

This patient has early iron deficiency without anemia, characterized by low ferritin (24 μg/L), low iron saturation (18%), and elevated transferrin (344 mg/dL), despite normal hemoglobin and hematocrit. 1

Laboratory Profile Interpretation

  • The combination of low transferrin saturation (<20%), elevated TIBC (399 μg/dL), elevated UIBC (328 μg/dL), and elevated transferrin represents a compensatory response where the body increases iron-carrying proteins to mobilize more iron for erythropoiesis 1

  • Ferritin of 24 μg/L confirms iron deficiency, as levels <30 μg/L in the absence of inflammation indicate true iron deficiency 2

  • The MCV of 97 fL (at upper limit of normal) and normal hemoglobin (13.2 g/dL) indicate that anemia has not yet developed, but iron stores are depleted 3

  • Normal CRP and negative autoimmune panel exclude inflammatory conditions that could confound ferritin interpretation 2

Recommended Management

Immediate Treatment

  • Initiate oral iron supplementation with ferrous sulfate 200 mg three times daily (or ferrous gluconate/ferrous fumarate as alternatives) 2

  • Take iron on an empty stomach with vitamin C (ascorbic acid) to enhance absorption, avoiding concurrent tea, coffee, calcium, or antacids 2, 1

  • Continue iron supplementation for three months after correction of iron parameters to replenish body stores 2

Investigation of Underlying Cause

For this female patient, the following causes must be evaluated:

  • Menstrual blood loss (menorrhagia) is the most common cause in premenopausal women, occurring in 5-10% of this population 2

  • Dietary insufficiency should be assessed through detailed dietary history, particularly vegetarian/vegan diets 1

  • Gastrointestinal blood loss must be considered, especially if menstrual history does not explain the deficiency 2, 1

  • Screen for celiac disease with tissue transglutaminase (tTG) antibody testing, as coeliac disease has ~5% pretest probability in iron deficiency 2, 1

  • Assess for NSAID use, which is a common cause of occult GI blood loss 2

Monitoring and Follow-up

  • Monitor hemoglobin and ferritin at 3-4 weeks; expect hemoglobin to rise by 2 g/dL if treatment is effective 2

  • Once iron parameters normalize, monitor hemoglobin and ferritin every three months for one year, then annually 2

  • If hemoglobin or ferritin falls below normal during follow-up, resume oral iron and consider further investigation 2

Critical Pitfalls to Avoid

  • Do not rely solely on serum iron levels (71 μg/dL in this case), as they have significant diurnal variation and can be normal in early iron deficiency 1, 3

  • Do not overlook iron deficiency in patients with normal hemoglobin; this patient demonstrates that iron depletion precedes anemia development 1, 3

  • Do not discontinue iron therapy prematurely once hemoglobin normalizes; continue for three months to replenish stores 2, 1

  • Failure to respond to oral iron (no rise in hemoglobin after 3-4 weeks) suggests poor compliance, continued blood loss, malabsorption, or misdiagnosis 2

When to Consider Parenteral Iron

  • Parenteral iron should only be used if there is intolerance to at least two oral iron preparations or documented non-compliance 2

  • Intravenous iron is preferred in patients with clinically active inflammatory bowel disease, hemoglobin <10 g/dL, or previous intolerance to oral iron 2

References

Guideline

Management of Iron Deficiency with Normal Iron Levels but High TIBC and Low Iron Saturation

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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