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DOI 10.1007/s10549-010-1178-3

Медицинская библиотека · Breast cancer research and treatment · 2010

Solid neuroendocrine carcinomas of the breast: metastases or primary tumors?

Richter-Ehrenstein Christiane, Arndt Juliane, Buckendahl Ann-Christin, Eucker Jan, Weichert Wilko, Kasajima Atsuko, Schneider Achim, Noske Aurelia

Сравнительное исследованиеОценочное исследованиеСтатьяПеревод пока не подготовлен

Аннотация

Neuroendocrine breast carcinomas are rare but may represent either metastatic or primary lesions. So far, clinical and preoperative histopathological examinations do not distinguish properly between a primary or metastatic breast tumor. Due to any possible consequences following an appropriate treatment, markers which may be helpful for such a distinguishment are needed. We addressed this study in order to evaluate the immunohistochemical expression of GCDFP-15 and mammaglobin in a subset of pure neuroendocrine breast carcinomas (n = 9) and compared the expression profile with a cohort of non-mammary neuroendocrine tumors (n = 99). We observed in our study that solid neuroendocrine breast carcinomas are characterized by the expression of estrogen and progesterone receptors as well as GCDFP-15 and/or mammaglobin. GCDFP-15 was expressed in 6 out of 9 cases, mammaglobin was positive in 4 out of 9 tumors. In contrast, neuroendocrine tumors of the non-mammary cohort expressed neither GCDFP-15 nor mammaglobin. We conclude that mammaglobin and GCDFP-15 as markers of epithelial breast origin may work as a new and reliable diagnostic tool to distinguish primary endocrine tumors of the breast from a metastatic neuroendocrine disease. This is of utmost importance, especially for surgical management.

Для цитирования: Richter-Ehrenstein Christiane, Arndt Juliane, Buckendahl Ann-Christin, Eucker Jan, Weichert Wilko, Kasajima Atsuko, Schneider Achim, Noske Aurelia. Solid neuroendocrine carcinomas of the breast: metastases or primary tumors?. Breast cancer research and treatment. 2010. DOI: 10.1007/s10549-010-1178-3.

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