# Primary Breast Lymphoma in Mexico: A 15-Year Retrospective Case Series From a Tertiary Center Suggesting a Distinctly Early Age at Presentation

**Authors:** Javier A Teco-Cortes, Juan J Navarrete-Pérez, Oscar E Sánchez-Castro, Omar de los Santos-Farrera

PMC · DOI: 10.7759/cureus.104497 · Cureus · 2026-03-01

## TL;DR

This study reports six cases of primary breast lymphoma in Mexico, noting that patients were diagnosed at a younger age than typically seen internationally.

## Contribution

The paper highlights a younger age at diagnosis for primary breast lymphoma in a Mexican population, suggesting potential regional differences.

## Key findings

- The mean age at diagnosis was 38.2 years, significantly younger than the typical sixth to seventh decades reported globally.
- Diffuse large B-cell lymphoma was the most common subtype, followed by classical Hodgkin lymphoma and B-lymphoblastic lymphoma.
- The findings suggest possible population-specific patterns in the epidemiology of primary breast lymphoma.

## Abstract

Background: Primary breast lymphoma (PBL) is a rare extranodal lymphoma involving breast tissue and most commonly affects women in the sixth to seventh decades of life. We describe a clinicopathological series of PBL cases diagnosed at a tertiary referral center in Mexico. Histologically, most cases correspond to B-cell non-Hodgkin lymphomas, particularly diffuse large B-cell lymphoma (DLBCL). Due to its rarity, available evidence is largely derived from small case series and retrospective analyses, highlighting the need for additional reports from diverse populations.

Methods: A retrospective, observational, descriptive study was conducted at a tertiary referral center in Mexico. All cases diagnosed as PBL between 2005 and 2020 were retrieved from the institutional pathology database. Inclusion criteria consisted of a histopathological diagnosis of primary lymphoma involving the breast with availability of complete histopathological material, including paraffin blocks and immunohistochemical studies. Descriptive statistics were used. Continuous variables are expressed as mean ± standard deviation, and categorical variables as absolute frequencies and percentages. Due to the small sample size, no inferential statistical analysis was performed.

Results: Six cases met the diagnostic criteria for PBL (N = 6), and all patients were women. The mean age at diagnosis was 38.2 ± 19 years (range, 19-66). DLBCL was the most frequent subtype (4/6, 66.7%), followed by classical Hodgkin lymphoma (1/6, 16.7%) and B-lymphoblastic lymphoma (1/6, 16.7%). Left breast involvement was observed in three cases, right-sided disease in one, bilateral presentation in one, and one case lacked specified laterality.

Conclusions: In this single-center Mexican series, patients were diagnosed at a younger age than typically reported in the international literature. DLBCL was the predominant subtype. These findings suggest the possibility of population-specific epidemiological patterns and underscore the need for larger regional studies to clarify potential differences in disease presentation.

## Linked entities

- **Diseases:** primary breast lymphoma (MONDO:0003661), diffuse large B-cell lymphoma (MONDO:0018905), classical Hodgkin lymphoma (MONDO:0009348)

## Full-text entities

- **Genes:** PWWP3A (PWWP domain containing 3A, DNA repair factor) [NCBI Gene 84939] {aka EXPAND1, HSPC211, MUM-1, MUM1}, CD5 (CD5 molecule) [NCBI Gene 921] {aka LEU1, T1}, KRT20 (keratin 20) [NCBI Gene 54474] {aka CD20, CK-20, CK20, K20, KRT21}, PAX5 (paired box 5) [NCBI Gene 5079] {aka ALL3, BSAP, PAX-5}, CD79A (CD79a molecule) [NCBI Gene 973] {aka IGA, IGAlpha, MB-1, MB1}, DNTT (DNA nucleotidylexotransferase) [NCBI Gene 1791] {aka TDT}
- **Diseases:** Hodgkin lymphoma (MESH:D006689), Burkitt lymphoma (MESH:D002051), B-cell non-Hodgkin lymphomas (MESH:D016393), breast carcinoma (MESH:D001943), extranodal lymphoma (MESH:D008223), mastitis (MESH:D008413), DLBCL (MESH:D016403), B-lymphoblastic lymphoma of the breast (MESH:D061325), FL (MESH:D008224), inflammatory (MESH:D007249), neuroendocrine carcinoma (MESH:D018278), MALT lymphoma (MESH:D018442), anaplastic large cell lymphoma (MESH:D017728), lobular carcinoma (MESH:D018275), B-lymphoblastic lymphoma (MESH:D054198), cutaneous pseudolymphoma (MESH:D019310), Hematolymphoid Tumors (MESH:D009369), medullary carcinoma (MESH:D018276)
- **Chemicals:** paraffin (MESH:D010232)
- **Species:** Homo sapiens (human, species) [taxon 9606], human gammaherpesvirus 4 (Epstein Barr virus, no rank) [taxon 10376]

## Full text

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## Figures

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## References

18 references — full list in the complete paper: https://tomesphere.com/paper/PMC12950993/full.md

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Source: https://tomesphere.com/paper/PMC12950993