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A Rare Case of Adenoid Cystic Breast Cancer: A Case Report and Literature Review
Elie Bterrani1,2, Doha Houcheimy3, David Karam3
1Division of Hematology-Oncology, Department of Medicine, Univeristy of Balamand, School of Medicine, Balamand, Lebanon.
Introduction:
Adenoid cystic carcinoma (AdCC) of the breast is an exceptionally rare malignancy, representing less than 0.1% of all breast cancers. Despite its triple-negative receptor profile, it typically follows an indolent course with excellent prognosis, distinct from the aggressive behavior usually seen in triple-negative breast cancers (TNBCs).
Case Presentation:
We report the case of a 48-year-old woman with a significant familial history of cancer who was diagnosed with breast AdCC. Imaging revealed a suspicious lesion in the left breast, and biopsy confirmed AdCC. Surgical resection showed a 58-mm, pT3, pN0(sn) triple-negative tumor with a low proliferative index. Genetic testing revealed a BRIP1 variant of uncertain significance (VUS). No adjuvant chemotherapy was given, and the patient remains in remission under surveillance.
Discussion:
This case highlights the diagnostic challenges of AdCC, including its resemblance to benign lesions on imaging and its overlap with high-grade TNBC histologically. While most AdCC cases are sporadic, the presence of a BRIP1 VUS in a patient with strong family history raises questions about possible hereditary implications. Management was based on current best practices, emphasizing surgical resection and selective use of radiotherapy.
Conclusion:
Breast AdCC, though rare, requires heightened clinical awareness for accurate diagnosis and management. This case underscores the potential role of genetic evaluation in rare breast cancer subtypes and the importance of continued case reporting to guide future recommendations.