Adenoid Cystic Carcinoma of the Breast: An Oncological Center's Experience

سال انتشار: 1401
نوع سند: مقاله ژورنالی
زبان: انگلیسی
مشاهده: 55

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شناسه ملی سند علمی:

JR_ARCHB-9-1_009

تاریخ نمایه سازی: 14 آذر 1402

چکیده مقاله:

Background: Adenoid cystic carcinoma of the breast (ACCB) is a rare breast malignancy. Despite often being a triple negative tumor, it has a favorable prognosis, with low rates of recurrence and progression. The ideal treatment of ACCB is debatable; thus, the aim of this study was to characterize a population diagnosed with ACCB and to evaluate the treatment outcomes. Methods: We performed a single-center retrospective analysis of patients with a histological diagnosis of ACCB treated at our dedicated Oncological Center between ۱۹۸۷ and ۲۰۲۰. The patients were identified in collaboration with the Anatomical Pathology Department, which also reviewed the surgical pathology reports. Results: Thirteen women with a median age of ۶۸ years old were diagnosed with ACCB. The most frequent clinical diagnosis was a breast nodule (n=۵); the preoperative image was suggestive of malignancy in nine patients, with seven being diagnosed with a ACCB in the preoperative biopsy. Regarding treatment, nine patients underwent conservative surgery, but three required re-excision. Sentinel lymph node biopsy (SLNB) was performed in seven patients, none revealing metastases; one patient had stage III ACCB and was initially treated with a modified radical mastectomy (MRM); the remaining were stage I (n=۷) and II (n=۵). Adjuvant radiotherapy was performed in eight patients, and two were initially proposed for chemotherapy but were considered unfit. With a median follow-up of ۱۲۳ months (۱۶-۴۰۷), one case of local recurrence and two cases of distant metastasis were identified, one of whom died of disease. Conclusion: ACCB is a rare tumor with a good prognosis; however, as demonstrated, it can present an aggressive behavior. Conservative surgery and adjuvant radiotherapy are the indicated treatment and SLNB may be omitted in grade ۱ tumors.

نویسندگان

Ana Margarida Correia

Surgical Oncology Department, Instituto Português de Oncologia do Porto Francisco Gentil, Porto, Portugal

Rafael Fernandes

General Surgery Department, Hospital de Santa Cruz, Centro Hospitalar de Lisboa Ocidental, Portugal

Teresa Dias

Surgical Oncology Department, Instituto Português de Oncologia do Porto Francisco Gentil, Porto, Portugal

Madalena Souto Moura

Anatomical Pathology Department, Instituto Português de Oncologia do Porto Francisco Gentil, Porto, Portugal