# Unveiling the Pernicious Truth: A Case Report on the Rare Presentation of Severe Vitamin B12 Deficiency

**Authors:** Olawale O Akinola, Anvitha Mandapati, Nathan Douthit

PMC · DOI: 10.7759/cureus.101860 · Cureus · 2026-01-19

## TL;DR

This case report highlights a rare presentation of severe vitamin B12 deficiency mimicking hemolytic anemia in a patient with Hashimoto’s thyroiditis.

## Contribution

The paper presents a unique clinical case where pernicious anemia was misdiagnosed as hemolytic anemia due to overlapping symptoms and lab findings.

## Key findings

- Severe vitamin B12 deficiency can present with hemolytic features, leading to confusion with autoimmune or microangiopathic processes.
- Pernicious anemia was confirmed by positive anti-intrinsic factor antibodies and responded rapidly to vitamin B12 replacement therapy.

## Abstract

Vitamin B₁₂ deficiency typically causes megaloblastic anemia but can rarely present with hemolytic features, leading to diagnostic confusion with autoimmune or microangiopathic processes. Pernicious anemia, an autoimmune cause of severe B₁₂ deficiency, is frequently underrecognized and may coexist with other autoimmune disorders.

We report a 45-year-old woman with Hashimoto’s thyroiditis who presented with dizziness, profound fatigue, and symptomatic anemia. Laboratory evaluation revealed severe macrocytic anemia (hemoglobin 3.5 g/dL, mean corpuscular volume (MCV) 136.9 fL) with thrombocytopenia, elevated lactate dehydrogenase (LDH) (2905 U/L), indirect hyperbilirubinemia, and suppressed haptoglobin, findings suggestive of hemolysis. Peripheral smear showed macrocytosis and marked anisopoikilocytosis without schistocytes. Coombs testing was negative, and G6PD levels were normal. Vitamin B₁₂ was severely reduced (73 pg/mL), and anti-intrinsic factor antibodies were positive, confirming pernicious anemia presenting as hemolytic anemia. Intensive intramuscular cyanocobalamin therapy led to rapid hematologic recovery, including normalization of platelet count within two weeks and improvement of hemoglobin to 8.4 g/dL.

Pernicious anemia can mimic hemolytic anemia, risking misdiagnosis as autoimmune hemolysis or thrombotic microangiopathy. Negative Coombs test, mild reticulocytosis relative to anemia severity, and macrocytosis provide critical diagnostic clues. Awareness of autoimmune clustering such as Hashimoto’s thyroiditis with pernicious anemia can prompt timely recognition. Early vitamin B₁₂ replacement reverses hematologic abnormalities and prevents irreversible neurologic damage.

## Linked entities

- **Chemicals:** vitamin B12 (PubChem CID 73415824), cyanocobalamin (PubChem CID 166596686)
- **Diseases:** Hashimoto’s thyroiditis (MONDO:0007699), pernicious anemia (MONDO:0008228), hemolytic anemia (MONDO:0003664)

## Full-text entities

- **Genes:** G6PD (glucose-6-phosphate dehydrogenase) [NCBI Gene 2539] {aka CNSHA1, G6PD1}, HP (haptoglobin) [NCBI Gene 3240] {aka HP2ALPHA2, HPA1S}
- **Diseases:** Anemia (MESH:D000740), trauma (MESH:D014947), AIHA (MESH:D000744), gastrointestinal or urinary symptoms (MESH:D012817), inflammation (MESH:D007249), syncope (MESH:D013575), malabsorption (MESH:D008286), neurologic damage (MESH:D020196), hematologic abnormalities (MESH:D006402), blurring of vision (MESH:D014786), nutritional deficiencies (MESH:D044342), hypothyroidism (MESH:D007037), G6PD deficiency (MESH:D005955), HUS (MESH:D006463), hepatosplenomegaly (MESH:C535727), dyspnea (MESH:D004417), thrombocytopenia (MESH:D013921), cyanosis (MESH:D003490), dizziness (MESH:D004244), macrocytic anemia (MESH:D000748), purpura (MESH:D011693), Autoimmune thyroid disease (MESH:D013967), thyroid disease (MESH:D013959), essential hypertension (MESH:D000075222), autoimmune diseases (MESH:D001327), nausea (MESH:D009325), macrocytosis (MESH:C564004), bleeding (MESH:D006470), renal impairment (MESH:D007674), sinus tachycardia (MESH:D013616), fatigue (MESH:D005221), chest pain (MESH:D002637), MAHA (MESH:D000743), icterus (MESH:D007565), thrombotic microangiopathy (MESH:D057049), B12 deficiency (MESH:D014806), megaloblastic (MESH:D000749), palpitations (MESH:D006331), TTP (MESH:D011697), hyperbilirubinemia (MESH:D006932), neurologic deficits (MESH:D009461), autoimmune gastritis (MESH:D005756), inherited disorders (MESH:D030342), seizures (MESH:D012640), autoimmune destruction (MESH:D008105), Pernicious anemia (MESH:D000752), reticulocytosis (MESH:D045262), degeneration of the spinal cord (MESH:D013118), iron deficiency anemia (MESH:D018798), neurologic sequelae (MESH:D009422), Hashimoto's thyroiditis (MESH:D050031), mass (MESH:C536030), marrow failure (MESH:D000080983), iron deficiency (MESH:D000090463), Hemolysis (MESH:D006461), nabothian cyst (MESH:D003560), systolic and diastolic heart failure (MESH:D054144)
- **Chemicals:** levothyroxine (MESH:D013974), oxygen (MESH:D010100), bilirubin (MESH:D001663), amiodarone (MESH:D000638), B12 (MESH:C034730), Iron (MESH:D007501), digoxin (MESH:D004077), Vitamin B12 (MESH:D014805), metoprolol (MESH:D008790), bumetanide (MESH:D002034)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

11 references — full list in the complete paper: https://tomesphere.com/paper/PMC12916071/full.md

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Source: https://tomesphere.com/paper/PMC12916071