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From the Departments of Pathology, and of Obstetrics and Gynecology, College of Physicians and Surgeons, Columbia University and the Obstetrical and Gynecological Service (The Sloane Hospital) of the Presbyterian Hospital, New York, NY.
Abstract
The thirty-first primary ovarian carcinoid tumor to be reported, one associated with the carcinoid syndrome, is described in a postmenopausal subject. It is demonstrated that the microscopic pattern of an ovarian carcinoid is similar to that of a granulosa cell tumor, requiring close attention to distinguishing nuclear details for differentiation.
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