卵巢富細(xì)胞纖維瘤24例臨床病理分析
[Abstract]:Objective: to investigate the clinical and pathological features of ovarian rich-cell fibroma. Methods: the clinicopathological data of 24 patients with ovarian rich cell fibroma treated by Department of Obstetrics and Gynecology affiliated to Fudan University from February 2008 to March 2017 were collected and the histological features and immunophenotype of the tumor were observed and followed up. Results: the age of 24 patients was 1770 years (mean 46.5 years). The clinical symptoms included ovarian mass, lower abdominal distending pain or hydrothorax and ascites. 2 patients had significantly elevated CA125 before operation. Cell-rich fibroma of ovary occurred in right ovary, left ovary and bilateral ovary in 1 case. The results showed that there were plenty of tumor cells and no obvious heterogeneity. The mitotic nuclei of 3 patients were active, the mitotic images were 5 ~ 7 / 10 high-power field (high power fields,HPF), and the tumor of 3 patients contained a small amount (less than 10%) of sex cord components. Luteinized cells were seen in 4 cases. Follow-up for 1 ~ 109 months showed no recurrence. Conclusion: ovarian cell-rich fibroma is a pure interstitial tumor with increased mitotic appearance with a small amount of sex cord and luteinization. Some patients with ascites of pleural effusion and CA125 were easily misdiagnosed as malignant tumor. In order to avoid misdiagnosis to affect the clinical diagnosis and treatment, it is of great significance to recognize the disease.
【作者單位】: 復(fù)旦大學(xué)附屬婦產(chǎn)科醫(yī)院病理科;
【分類號(hào)】:R737.31
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