Annals of Diagnostic Pathology
Volume 12, Issue 1 , Pages 4-11, February 2008

Basaloid carcinoma of the breast: a review of 9 cases, with delineation of a possible clinicopathologic entity

Presented in part at the 94th Meeting of the United States and Canadian Academy of Pathology, San Antonio, Tex, March 2005.

  • Janez Lamovec, MD

      Affiliations

    • Department of Pathology, Institute of Oncology, SI-1000 Ljubljana, Slovenia
  • ,
  • Giovanni Falconieri, MD

      Affiliations

    • Department of Pathology and Laboratory Medicine, Division of Anatomic Pathology, General Hospital S. Maria della Misericordia, I 33100 Udine UD, Italy
    • Corresponding Author InformationCorresponding author. Tel.: +39 0432 552826; fax: +39 0432 552830.
  • ,
  • Tiziana Salviato, MD

      Affiliations

    • Department of Pathology, Centro di Riferimento Oncologico, I-33081 Aviano PN, Italy
  • ,
  • Stefano Pizzolitto, MD

      Affiliations

    • Department of Pathology and Laboratory Medicine, Division of Anatomic Pathology, General Hospital S. Maria della Misericordia, I 33100 Udine UD, Italy

published online 04 October 2007.

Abstract 

Basaloid carcinoma of the breast (BCB) is an unusual neoplasm composed of basal-type neoplastic cells similar to those found in adenoid cystic carcinoma (ACC), although lacking distinctive features such as a cribriform pattern, a dual neoplastic population (epithelial-myoepithelial/basaloid), and stromal deposits of basement membrane–like material. In this article, we present 9 cases of breast cancer showing overall/predominant basaloid morphology. Patients' ages ranged from 47 to 75 years (mean, 61.4 years). Surgical treatment included mastectomy or quadrant excision with or without axillary dissection. Most tumors had a circumscribed outline and ranged in size from 1.3 to 5.5 cm (mean, 2.5 cm). Microscopically, they featured sheets, nests, and cords of proliferating basaloid tumor cells with ovoid, hyperchromatic nuclei with inconspicuous nucleoli and scant cytoplasm. No foci with characteristics of ACC were found in any of the tumors. Transition into pleomorphic basaloid carcinoma with foci of high-grade ductal carcinoma in situ plus infiltrating ductal carcinoma (IDC) and admixture with grade 3 ductal and sarcomatoid carcinoma was seen in 2 cases. Tumor cells were positive for wide-spectrum keratins and epithelial membrane antigen (9/9) and high-molecular-weight keratins (7/9). They were negative for smooth muscle actin, p63, calponin, and CD10 in all tested cases. Estrogen receptor, progesterone receptor, and HER-2 were negative. Axillary lymph node metastases were seen in 3 cases. At follow-up (range, 10-169 months), 5 patients were alive, 1 with evidence of contralateral breast cancer. Three patients died: one of disseminated BCB metastases, another of liver cirrhosis, and one of disseminated estrogen receptor/progesterone receptor–positive contralateral IDC. One patient was lost to follow-up. We concluded that BCB has some phenotypic and immunohistochemical features enabling its distinction from ACC or IDC. It appears to be a morphological and possibly a clinical entity. Compared with ACC, BCB appears to be more aggressive and may entail a more guarded prognosis.

Keywords: Breast tumors, Basaloid carcinoma, Immunohistochemistry

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PII: S1092-9134(07)00016-0

doi:10.1016/j.anndiagpath.2007.01.009

Annals of Diagnostic Pathology
Volume 12, Issue 1 , Pages 4-11, February 2008