Is autoimmune gastritis the most likely diagnosis for a patient with iron deficiency, low iron saturation, and a positive parietal cell antibody (PCA) test, despite a negative intrinsic factor antibody (IFA) test?

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Differential Diagnosis

  • Single most likely diagnosis
    • Autoimmune gastritis: This is the most likely diagnosis given the patient's positive parietal cell antibody test, low iron, and low iron saturation. The presence of parietal cell antibodies is a hallmark of autoimmune gastritis, which can lead to impaired iron absorption and chronic iron deficiency anemia.
  • Other Likely diagnoses
    • Iron deficiency anemia due to chronic blood loss: Although the patient has a positive parietal cell antibody test, it's still possible that she has another source of chronic blood loss, such as menstrual bleeding or gastrointestinal bleeding, that's contributing to her iron deficiency.
    • Celiac disease: Celiac disease can cause malabsorption of iron and other nutrients, leading to iron deficiency anemia. The patient's long-standing history of low iron levels could be consistent with celiac disease.
  • Do Not Miss (ddxs that may not be likely, but would be deadly if missed.)
    • Gastric cancer: Although rare, gastric cancer can cause iron deficiency anemia and should be considered in the differential diagnosis, especially in patients with a long history of unexplained iron deficiency.
    • Gastrointestinal bleeding from other sources (e.g., ulcers, vascular ectasias): These conditions can cause chronic blood loss and iron deficiency anemia, and it's essential to rule them out to prevent potentially life-threatening complications.
  • Rare diagnoses
    • Atrophic gastritis due to other causes (e.g., Helicobacter pylori infection, chronic use of proton pump inhibitors): These conditions can also lead to impaired iron absorption and iron deficiency anemia, although they are less likely given the patient's positive parietal cell antibody test.
    • Hereditary iron-refractory iron deficiency anemia: This is a rare genetic disorder that can cause iron deficiency anemia, but it's unlikely given the patient's positive parietal cell antibody test and long-standing history of low iron levels.

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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