【摘要】：目的探討復(fù)發(fā)性子宮苗勒源腺纖維瘤臨床病理特征。方法選取2003年2月至2014年2月該院收治的復(fù)發(fā)性子宮苗勒源腺纖維瘤患者8例,分析其臨床數(shù)據(jù),總結(jié)子宮苗勒源腺纖維瘤的病理特點。結(jié)果 8例復(fù)發(fā)性子宮苗勒源腺纖維瘤患者可在宮頸外或者宮腔內(nèi)見分葉狀贅生物,由良性上皮和間葉組織形成。免疫組化顯示,8例患者均表達(dá)雌激素受體(ER),部分患者表達(dá)孕激素受體(PR)、平滑肌肌動蛋白(SMA)、CD10和p53,而Ki-67(+)均值平均為8%。結(jié)論復(fù)發(fā)性子宮苗勒源腺纖維瘤臨床病理無特異性變化,與腺肉瘤鑒別診斷困難,僅CD10和Ki-67可能有助于診斷。
[Abstract]:Objective to investigate the clinicopathological features of recurrent uterine Muller adenofibroma. Methods from February 2003 to February 2014, 8 patients with recurrent uterine Muller adenofibroma were selected. The clinical data were analyzed and the pathological characteristics of uterine Muller adenofibroma were summarized. Results in 8 patients with recurrent uterine Muller adenofibroma, lobulated vegetation was found outside the cervix or in the uterine cavity, which was formed by benign epithelial and mesobal tissue. The expression of progesterone receptor (PR), smooth muscle actin (SMA), CD10 and p53 was found in all 8 patients with estrogen receptor (ER), while the mean value of Ki-67 () was 8%. Conclusion recurrent uterine Muller adenofibroma has no specific clinicopathological changes and is difficult to differentiate from adenosarcoma. Only CD10 and Ki-67 may be helpful in the diagnosis of recurrent adenofibroma.
【作者單位】： 海南省瓊海市人民醫(yī)院病理科;
【分類號】：R737.33

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