Adenoid Cystic Carcinoma of the Breast: A Case Report.

Adenoid cystic carcinoma Breast cancer Favorable prognosis Mammary tumor Triple-negative

Journal

Case reports in oncology
ISSN: 1662-6575
Titre abrégé: Case Rep Oncol
Pays: Switzerland
ID NLM: 101517601

Informations de publication

Date de publication:
Historique:
received: 21 08 2019
accepted: 22 08 2019
entrez: 15 10 2019
pubmed: 15 10 2019
medline: 15 10 2019
Statut: epublish

Résumé

Adenoid cystic carcinomas (ACCs) are malignant tumors that most often occur in the salivary glands and bronchi, with occurrence in the breast being rare. ACCs of the breast reportedly give rise to few lymph node metastases or distant metastases and have a favorable prognosis. A 56-year-old woman with a left breast mass identified by mammographic screening was examined at our institute. Breast ultrasound revealed a sharply marginated, hypoechoic mass 12.7 × 9.4 × 8.7 mm in size in the upper outer quadrant of the left breast, and a vacuum-assisted biopsy (VAB) was performed at the mass site. Pathological examination of the VAB specimen revealed atypical cells with a cribriform growth pattern, and mucosal fluid surrounding tumor nests and within tumor ducts. The area around the tumor nests and inside of tumor ducts were also positively stained with alcian blue. These findings, we reached a pathological diagnosis of ACC. The preoperative diagnosis was stage I (cT1N0M0) triple-negative left breast cancer. Surgery consisted of breast-conserving surgery and sentinel node biopsy. The excised specimen was a 15.0 × 12.1 × 9.7 mm mass with a greyish white cut surface. Pathological examination of the excised specimen revealed a so-called adenoid cystic pattern. Results from immunohistochemical staining were identical to those from a VAB specimen, as they were estrogen receptor-negative, progesterone receptors-negative, and human epidermal growth factor receptor 2-negative, with low Ki67 expression. The final diagnosis, given the above findings, was left breast cancer (ACC) pT1N0M0 stage I triple-negative subtype.

Identifiants

pubmed: 31607886
doi: 10.1159/000502949
pii: cro-0012-0698
pmc: PMC6787413
doi:

Types de publication

Case Reports

Langues

eng

Pagination

698-703

Informations de copyright

Copyright © 2019 by S. Karger AG, Basel.

Déclaration de conflit d'intérêts

The authors declare that they have no conflicts of interest to disclose.

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Auteurs

Shinichiro Kashiwagi (S)

Department of Breast and Endocrine Surgery, Osaka City University Graduate School of Medicine, Osaka, Japan.

Yuka Asano (Y)

Department of Breast and Endocrine Surgery, Osaka City University Graduate School of Medicine, Osaka, Japan.

Sae Ishihara (S)

Department of Breast and Endocrine Surgery, Osaka City University Graduate School of Medicine, Osaka, Japan.

Tamami Morisaki (T)

Department of Breast and Endocrine Surgery, Osaka City University Graduate School of Medicine, Osaka, Japan.

Tsutomu Takashima (T)

Department of Breast and Endocrine Surgery, Osaka City University Graduate School of Medicine, Osaka, Japan.

Sayaka Tanaka (S)

Department of Diagnostic Pathology, Osaka City University Graduate School of Medicine, Osaka, Japan.

Ryosuke Amano (R)

Department of Hepato-Biliary-Pancreatic Surgery, Osaka City University Graduate School of Medicine, Osaka, Japan.

Masahiko Ohsawa (M)

Department of Diagnostic Pathology, Osaka City University Graduate School of Medicine, Osaka, Japan.

Kosei Hirakawa (K)

Department of Breast and Endocrine Surgery, Osaka City University Graduate School of Medicine, Osaka, Japan.
Department of Gastrointestinal Surgery, Osaka City University Graduate School of Medicine, Osaka, Japan.

Masaichi Ohira (M)

Department of Breast and Endocrine Surgery, Osaka City University Graduate School of Medicine, Osaka, Japan.
Department of Gastrointestinal Surgery, Osaka City University Graduate School of Medicine, Osaka, Japan.

Classifications MeSH