Evidence map›Paper›PMID 41717155›Full record

ArticleCureus2026

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

Olawale O Akinola, Anvitha Mandapati, Nathan Douthit

Abstract readCase Reports
In one paragraph

Article in Cureus, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Olawale O AkinolaInternal Medicine, East Alabama Medical Center, Opelika, USA.
Anvitha MandapatiInternal Medicine, Edward Via College of Osteopathic Medicine, Auburn, USA.
Nathan DouthitInternal Medicine, East Alabama Medical Center, Opelika, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

clinical casehemolytic anaemiaintramedullary hemolysispernicious-anemiavitamin b 12 deficiency

Identifiers

PMID41717155
PMCPMC12916071

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