# T-cell Acute Lymphoblastic Leukemia Presenting With Bilateral Breast Masses

**Authors:** Hala Alsoukhni, Shirin Al-Mharat, Ishraq Abu Darweesh, Amani Alrousan, Maher Bani Essa

PMC · DOI: 10.7759/cureus.103002 · Cureus · 2026-02-04

## TL;DR

A 20-year-old woman with sudden breast enlargement was diagnosed with rare T-cell acute lymphoblastic leukemia.

## Contribution

This case highlights the rare presentation of T-cell ALL as bilateral breast masses in a young woman.

## Key findings

- Breast ultrasound showed heterogeneous parenchyma and enlarged lymph nodes in a patient with T-cell ALL.
- T-cell ALL presenting as breast masses can achieve remission with the Berlin-Frankfurt-Münster protocol.
- T-cell lymphoblastic lymphoma was confirmed via breast core biopsy and bone marrow examination.

## Abstract

T-cell lymphoma involvement of the breast is rare and represents a diagnostic challenge. Here, we present a case of T-cell acute lymphoblastic leukemia (ALL) in a 20-year-old woman who presented in September 2023 with a history of bilateral breast enlargement associated with general weakness, weight loss, and a feeling of heat, which had lasted for about two months. She was examined clinically and found to have huge bilateral breast enlargement. A breast ultrasound (US) was performed and showed a diffuse abnormal heterogeneous parenchymal appearance of both breasts with multiple enlarged bilateral axillary lymph nodes. The patient was referred to the Military Cancer Center for breast core biopsy, which showed bilateral breast involvement by T-cell lymphoblastic lymphoma. Subsequently, bone marrow examination revealed T-cell ALL. The patient was started on the augmented Berlin-Frankfurt-Münster protocol, achieved complete remission, and maintained it for two years after diagnosis. ALL in the breast is rare but should be considered especially in young patients presenting with sudden breast masses.

## Linked entities

- **Diseases:** T-cell acute lymphoblastic leukemia (MONDO:0004963)

## Full-text entities

- **Genes:** CD99 (CD99 molecule (Xg blood group)) [NCBI Gene 4267] {aka HBA71, MIC2, MIC2X, MIC2Y, MSK5X}, DNTT (DNA nucleotidylexotransferase) [NCBI Gene 1791] {aka TDT}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, CD7 (CD7 molecule) [NCBI Gene 924] {aka GP40, LEU-9, TP41, Tp40}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, CD1A (CD1a molecule) [NCBI Gene 909] {aka CD1, FCB6, HTA1, R4, T6}
- **Diseases:** node (MESH:D012804), pain (MESH:D010146), skin erythema (MESH:D012871), PTCL (MESH:D016411), Cancer (MESH:D009369), weakness (MESH:D018908), ALCL (MESH:D017728), adult T-cell lymphoma (MESH:D015459), edema (MESH:D004487), pericardial and pleural effusion (MESH:D010996), lymphadenopathy (MESH:D008206), AML (MESH:D015470), hematologic malignancy (MESH:D019337), pericardial effusion (MESH:D010490), systemic disease (MESH:D034721), T-cell LBL (MESH:D016399), Breast Masses (MESH:D061325), Leukemia (MESH:D007938), T-cell ALL (MESH:D054218), ALL (MESH:D054198), marrow (MESH:D001855), weight loss (MESH:D015431), leukocytosis (MESH:D007964), extranodal lymphomas (MESH:D008223), lymphomatous disease (MESH:D013967), LNE (MESH:D000072717), breast cancer (MESH:D001943), mycosis fungoides (MESH:D009182), thrombocytosis (MESH:D013922), mediastinal mass (MESH:D008477), tenderness (MESH:D063806)
- **Chemicals:** Oncovin (MESH:D014750), uric acid (MESH:D014527), Methotrexate (MESH:D008727), Prednisolone (MESH:D011239), H&amp;E (MESH:D006371), Doxorubicin (MESH:D004317), hematoxylin (MESH:D006416), Purinethol (MESH:D015122), eosin (MESH:D004801)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12966808/full.md

## References

19 references — full list in the complete paper: https://tomesphere.com/paper/PMC12966808/full.md

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Source: https://tomesphere.com/paper/PMC12966808