Abstract

Primary ovarian carcinoid tumors are rare neoplasms that constitute less than 0.1% of all ovarian carcinomas. However, carcinoid tumors metastatic to ovaries are more common. Cell proliferative rate is an important factor in the determination of neuroendocrine tumor prognosis. Limited data are available as regards Ki67 proliferation index in predicting the physiological features of carcinoid tumors involving the ovary. Pathology files of Mayo Clinic Rochester (1995–2014) were searched, and clinical information was collected from medical records. All cases were stained with an antibody against Ki67, and digital analysis was performed with digital imaging analysis. A total of 36 cases (median age 64 years, range 33–83 years), including 9 primary (median age 68 years, range 33–73 years) and 27 metastatic carcinoid cases (median age 64 years, range 36–83 years), were investigated in the current study. Seven out of nine (77.8%) primary ovarian carcinoids are associated with mature teratoma. Twenty two metastatic carcinoids (81.5%) were from the GI tract, four (14.8%) from the pancreas, and one (3.7%) from the posterior thorax location. There was significant difference of Ki67 index between primary (median 2.3%, range, 0.6–8.4%) and metastatic carcinoid tumors (median 9.7%, range, 1.3–46.7%) (p = 0.002). The survival time is much shorter among patients with metastatic carcinoid tumor (median survival 5.8 years) comparing to primary ovarian carcinoid tumor (median 14.2 years) (p = 0.0005). A strong association between Ki67 index and patient survival time was identified (Hazard ratio for 1-percentage point increase 1.11, p = 0.001). Comparing to primary ovarian carcinoid tumor, metastatic carcinoid usually exhibits a higher Ki67 index and a worse outcome.

Highlights

  • Primary ovarian carcinoid tumors are rare neoplasms that constitute about 0.1% of all ovarian carcinomas and less than 1% of all carcinoid tumors [1]. This entity was first described by Stewart et al in 1939 and subsequent studies have demonstrated that a majority of primary ovarian carcinoids occur in association with mature cystic teratoma, with a small number in pure form

  • A total of 36 cases including 9 ovarian primary and 27 metastatic carcinoid cases were investigated in the current study

  • This is similar to what we found in the current study, in which the median survival time was 14.2 years for primary and 5.8 years for metastatic ovarian carcinoid patients

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Summary

Introduction

Primary ovarian carcinoid tumors are rare neoplasms that constitute about 0.1% of all ovarian carcinomas and less than 1% of all carcinoid tumors [1]. This entity was first described by Stewart et al in 1939 and subsequent studies have demonstrated that a majority of primary ovarian carcinoids occur in association with mature cystic teratoma, with a small number in pure form. Comparing to primary ovarian carcinoid tumors, neuroendocrine tumors from extra ovarian origin with metastasis to the ovary are relatively common. These tumors tend to arise from gastrointestinal origin, which usually involves bilateral ovaries

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