# ABO Discrepancy in a Patient With Plasma Cell Myeloma

**Authors:** Sumaiyah Adzahar, Adibah Daud, Syamihah Mardhiah A Razak, Kamariah Abdul Jalil, Mohammad Hudzaifah Nordin, Muhammad 'Aqil Nazahah Mohamad Mustafa, Daniel Hazim Mohd Shukri, Azzahra Azhar, Sharifah Sakinah Syed Abdul Rahman, Razan Hayati Zulkeflee

PMC · DOI: 10.7759/cureus.67096 · 2024-08-17

## TL;DR

This paper discusses a rare case of blood type discrepancy in a patient with plasma cell myeloma, highlighting the challenges in blood typing and transfusion management.

## Contribution

The novelty lies in identifying a unique ABO discrepancy caused by B antigen loss in a plasma cell myeloma patient.

## Key findings

- The patient's blood type discrepancy was due to B antigen loss caused by plasma cell myeloma.
- Type III discrepancies are common in multiple myeloma, but this case presented a distinct mechanism.
- Thorough evaluation is essential to manage transfusion risks in patients with antigen alterations.

## Abstract

ABO discrepancies in plasma cell myeloma (PCM) present unique challenges in blood typing tests and transfusion management. We present the case of a 51-year-old male with PCM who exhibited discrepancies between forward and reverse blood grouping. Further investigation revealed that the patient's blood type was a variant of blood group B. While type III discrepancies, typically characterized by elevated globulin levels causing false-positive reactions in both forward and reverse blood grouping, are common in multiple myeloma, our case differed due to the loss of B antigens secondary to the malignant condition. This caused a discrepancy in forward blood grouping. The rarity of ABO discrepancies in multiple myeloma underscores the importance of thorough evaluation. Awareness of potential antigen alterations in such patients is crucial to ensure safe transfusion practices.

## Linked entities

- **Diseases:** plasma cell myeloma (MONDO:0009693), multiple myeloma (MONDO:0009693)

## Full-text entities

- **Genes:** ABO (ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase) [NCBI Gene 28] {aka A3GALNT, A3GALT1, GTA, GTB, NAGAT}
- **Diseases:** PCM (MESH:D009101), malignant condition (MESH:D009369)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11405539/full.md

---
Source: https://tomesphere.com/paper/PMC11405539