Abstract
Both primary and secondary carcinoid tumours of the breast have been described. There has been considerable interest in primary carcinoid tumours since the description by Cubilla and Woodruff1 of ten cases (including two in the addendum) in 1977. In their series, the patients were all female, with a mean age of 54 years. Four of the ten patients had died with widespread metastatic tumour and a fifth was alive with disseminated disease. All the patients with tumours less than 2 cm in diameter were alive. Other reports of primary carcinoid tumours of the breast have sub-sequently appeared in the literature, including one in a male who had bilateral mammary neoplasms and an increased urinary excretion of norepinephrine2. The tumours are usually well circumscribed. On histological examination they are composed of solid nests of cells with poorly defined outlines and a low mitotic rate, set within a very vascular stroma (Figure 15.1). Ribbon-like and glandular patterns also occur (Figures 15.2 and 15.3). Sometimes the cells show marked pleo-morphism (Figure 15.4). Argyrophil granules can be demonstrated by a modified Grimelius technique as shown in Figures 15.5 and 15.6, but argentaffin granules are usually absent. Neurosecretory granules can be indentified on electron microscopy in some cases.
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© 1984 Rosemary R. Millis
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Millis, R.R. (1984). Special Types of Mammary Carcinoma 2. In: Atlas of Breast Pathology. Current Histopathology, vol 7. Springer, Dordrecht. https://doi.org/10.1007/978-94-009-6589-8_17
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DOI: https://doi.org/10.1007/978-94-009-6589-8_17
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