# Upgrade to malignancy after excision of MRI-only B3 breast lesions: should the size and histological type of the lesion be considered for therapeutic management?

**Authors:** Javier del Riego, Claudia Estandía, Cecilia Aynes, Adriana Campmany, Fiona Pallarés, Sergi Triginer, Natalia Papaleo, Aida López, Oscar Aparicio, Elsa Dalmau, Lidia Tortajada

PMC · DOI: 10.1186/s13244-025-02177-1 · Insights into Imaging · 2026-01-12

## TL;DR

This study finds that larger size, not histological type, predicts malignancy in MRI-only B3 breast lesions, suggesting size can guide treatment decisions.

## Contribution

The study identifies lesion size as a key predictor of malignancy upgrade in MRI-only B3 lesions, independent of histological type.

## Key findings

- 11.9% of MRI-only B3 lesions were upgraded to malignancy after excision.
- Lesion size >20 mm was significantly associated with malignancy upgrade.
- Conservative management may be safe for flat epithelial atypia lesions <20 mm.

## Abstract

To determine the rate of malignancy upgrade in MRI-only B3 lesions and to identify clinical, imaging, and histological features that can predict upgrade.

This retrospective single-center study included MRI-only lesions diagnosed as B3 after MRI-guided vacuum-assisted biopsy and excised between January 2007 and March 2023. We calculated upgrade rates for the entire series and for subgroups based on possible risk factors. To analyze variables considered risk factors for upgrade, we used logistic regression, calculating odds ratios (OR) and their 95% confidence intervals (CI).

Of 592 lesions biopsied, 89 (15.03%) were classified as B3. After excluding 30 lesions because excisional specimen results were unavailable, we analyzed 59 lesions in 51 patients. Biopsy classified 15 (25.4%) lesions as pure atypical ductal hyperplasia (ADH), 27 (45.8%) as pure flat epithelial atypia (FEA), 12 (20.3%) as mixed lesions, and 5 (8.5%) as lobular neoplasia. A total of 7 (11.9%) lesions were upgraded to malignancy (71.4% to ductal carcinoma in situ, 14.3% to invasive ductal carcinoma, and 4.3% to invasive lobular carcinoma). Although histological type was not associated with upgrade to malignancy (p = 0.47), 20% of pure ADH and only 3.7% of pure FEA lesions were upgraded. Larger lesion size on MRI was associated with upgrade [6.25% of lesions ≤ 20 mm vs. 36.4% of those > 20 mm, p = 0.02; OR 8.57 (95% CI: 1.57‒46.71) p = 0.01].

Lesion size may predict upgrade in MRI-only B3 lesions independent of histological type; imaging follow-up may suffice for FEA lesions measuring < 20 mm.

Considering lesion size and histological type could help define the management of MRI-only lesions classified as B3 after MRI-guided vacuum-assisted biopsy.

The management of MRI-only B3 lesions has yet to be established.Lesion size is a relevant factor to consider when deciding clinical management in MRI-only B3 lesions.Conservative management appears to be safe in selected flat epithelial atypia lesions (< 20 mm).

The management of MRI-only B3 lesions has yet to be established.

Lesion size is a relevant factor to consider when deciding clinical management in MRI-only B3 lesions.

Conservative management appears to be safe in selected flat epithelial atypia lesions (< 20 mm).

## Linked entities

- **Diseases:** breast cancer (MONDO:0004989), ductal carcinoma in situ (MONDO:0005023), invasive ductal carcinoma (MONDO:0004953), invasive lobular carcinoma (MONDO:0005051)

## Full-text entities

- **Genes:** ADH1A (alcohol dehydrogenase 1A (class I), alpha polypeptide) [NCBI Gene 124] {aka ADH1}, ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}, PGR (progesterone receptor) [NCBI Gene 5241] {aka NR3C3, PR}, EREG (epiregulin) [NCBI Gene 2069] {aka EPR, ER, Ep}
- **Diseases:** invasive ductal carcinoma (MESH:D044584), carcinoma in situ (MESH:D002278), B3 (OMIM:120050), lesion (MESH:D009059), breast (MESH:D061325), like (MESH:C537419), apocrine adenosis (MESH:D005348), mucocele (MESH:D009078), breast cancer (MESH:D001943), fibroepithelial lesion (MESH:D018225), synchronous (MESH:D009378), papillary lesions (MESH:D002291), LN lobular neoplasia (MESH:D009369), ADH lesions (MESH:D002285), invasive (MESH:D009361), FEA (MESH:D009375), breast disease (MESH:D001941), atypical lobular hyperplasia (MESH:D018275), LCIS (MESH:D000071960)
- **Chemicals:** eosin (MESH:D004801), paraffin (MESH:D010232), hematoxylin (MESH:D006416), formalin (MESH:D005557), FEA (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

2 references — full list in the complete paper: https://tomesphere.com/paper/PMC12796027/full.md

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Source: https://tomesphere.com/paper/PMC12796027