# Unmasking Pernicious Anemia: A Reversible Cause of Pancytopenia Due to Severe Vitamin B12 Deficiency

**Authors:** Bola Habeb, Sandy Khair, Amber Reid

PMC · DOI: 10.7759/cureus.87911 · Cureus · 2025-07-14

## TL;DR

This paper discusses pernicious anemia, an autoimmune condition causing severe vitamin B12 deficiency, which can lead to pancytopenia and is often misdiagnosed as more serious blood disorders.

## Contribution

The paper emphasizes the importance of recognizing pernicious anemia as a reversible cause of pancytopenia to avoid unnecessary invasive procedures.

## Key findings

- Pernicious anemia is a common cause of vitamin B12 deficiency in developed countries.
- Severe B12 deficiency can mimic leukemia or aplastic anemia, leading to misdiagnosis.
- Early treatment with parenteral B12 can reverse hematologic issues and prevent neurologic damage.

## Abstract

Vitamin B12 (cobalamin) is a vital cofactor in DNA synthesis and hematopoiesis, and its deficiency can lead to a wide spectrum of clinical manifestations, ranging from asymptomatic macrocytosis to severe hematologic and neurologic complications. While megaloblastic anemia is the most common presentation, prolonged or profound deficiency can result in pancytopenia due to ineffective hematopoiesis and intramedullary cell death. This can mimic more serious bone marrow disorders, including leukemia or aplastic anemia, potentially leading to invasive diagnostic procedures if the deficiency is not promptly recognized. Pernicious anemia is the most common cause of vitamin B12 deficiency in developed countries. It is an autoimmune condition characterized by intrinsic factor deficiency due to antibodies targeting either intrinsic factor itself or gastric parietal cells. It often presents insidiously and is frequently diagnosed late, typically after complications such as pancytopenia or irreversible neurologic damage have developed. Timely identification and treatment with parenteral vitamin B12 can lead to rapid hematologic recovery and prevention of permanent neurologic injury, highlighting the importance of considering pernicious anemia in the differential diagnosis of pancytopenia.

## Linked entities

- **Chemicals:** Vitamin B12 (PubChem CID 73415824), cobalamin (PubChem CID 73415824)
- **Diseases:** Pernicious anemia (MONDO:0008228), megaloblastic anemia (MONDO:0001700), leukemia (MONDO:0004355), aplastic anemia (MONDO:0013879)

## Full-text entities

- **Genes:** SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}, HP (haptoglobin) [NCBI Gene 3240] {aka HP2ALPHA2, HPA1S}, CMPK1 (cytidine/uridine monophosphate kinase 1) [NCBI Gene 51727] {aka CK, CMK, CMPK, UMK, UMP-CMPK, UMPK}, GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}, TGM2 (transglutaminase 2) [NCBI Gene 7052] {aka G(h), TG(C), TGC, hTG2, tTG}, TF (transferrin) [NCBI Gene 7018] {aka HEL-S-71p, PRO1557, PRO2086, TFQTL1}
- **Diseases:** neurologic complications (MESH:D002493), celiac (MESH:D002446), ecchymosis (MESH:D004438), fatigue (MESH:D005221), Psychiatric (MESH:D001523), autoimmune condition (MESH:D001327), leukopenia (MESH:D007970), autoimmune hemolytic anemia (MESH:D000744), hypertension (MESH:D006973), ineffective erythropoiesis (MESH:C563479), malabsorption (MESH:D008286), melena (MESH:D008551), hematologic malignancies (MESH:D019337), hemolysis (MESH:D006461), poor (MESH:D009123), vibration sense (MESH:D053421), EBV (MESH:D020031), bone marrow disorders (MESH:D001855), chronic atrophic gastritis (MESH:D005757), psychosis (MESH:D011618), gastrointestinal bleeding (MESH:D006471), spastic paraparesis (MESH:D020336), transient ischemic attack (MESH:D002546), B12 deficiency (MESH:D014806), neurologic deficits (MESH:D009461), dietary insufficiency (MESH:D000309), macrocytosis (MESH:C564004), complications (MESH:D008107), hyperlipidemia (MESH:D006949), cytopenias (MESH:D006402), bacterial overgrowth (MESH:D001765), loss of proprioception (MESH:D020886), dyspnea (MESH:D004417), urinary tract infection (MESH:D014552), macrocytic anemia (MESH:D000748), diabetes mellitus (MESH:D003920), dementia (MESH:D003704), weakness (MESH:D018908), bone marrow failure syndromes (MESH:D000080983), memory loss (MESH:D008569), thyroid dysfunction (MESH:D013959), Pernicious Anemia (MESH:D000752), aplastic anemia (MESH:D000741), neurologic damage (MESH:D020196), motor or sensory deficits (MESH:D001289), megaloblastic anemia (MESH:D000749), hematologic and neurologic complications (MESH:D011250), cognitive symptoms (MESH:D019954), deficiency (MESH:D007153), intrinsic factor deficiency (MESH:C563242), hematuria (MESH:D006417), hepatitis (MESH:D056486), bacteriuria (MESH:D001437), degeneration of the spinal cord (MESH:D013118), thrombocytopenia (MESH:D013921), neuropathy (MESH:D009422), glossitis (MESH:D005928), depression (MESH:D003866), cognitive impairment (MESH:D003072), Crohn's disease (MESH:D003424)
- **Chemicals:** losartan (MESH:D019808), metformin (MESH:D008687), over-the-counter medications (-), Vitamin B12 (MESH:D014805), oxygen (MESH:D010100), urobilinogen (MESH:D014558), homocysteine (MESH:D006710), B12 (MESH:C034730), Iron (MESH:D007501), methylmalonic acid (MESH:D008764), simvastatin (MESH:D019821), alcohol (MESH:D000438), nifedipine (MESH:D009543), hydrochlorothiazide (MESH:D006852)
- **Species:** human gammaherpesvirus 4 (Epstein Barr virus, no rank) [taxon 10376], Nicotiana tabacum (American tobacco, species) [taxon 4097], hepatitis C virus [taxon 11103], Hepatitis B virus (no rank) [taxon 10407], Human immunodeficiency virus 1 (no rank) [taxon 11676], Hepatovirus A (no rank) [taxon 12092], Human immunodeficiency virus (species) [taxon 12721], Homo sapiens (human, species) [taxon 9606]
- **Mutations:** A1C, L to 1,035

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12349174/full.md

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12349174/full.md

## References

17 references — full list in the complete paper: https://tomesphere.com/paper/PMC12349174/full.md

---
Source: https://tomesphere.com/paper/PMC12349174