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子宫上皮样滋养细胞肿瘤的临床病理分析

[Clinicopathologic analysis of uterine epithelioid trophoblastic tumor].

作者信息

Liang Yun, Chen Xiao-duan, Lü Bing-jian, Shi Hai-yan, Zhang Xiao-fei

机构信息

Department of Pathology, Affiliated Women's Hospital, School of Medicine, Zhejiang University, Hangzhou 310006, China.

出版信息

Zhonghua Bing Li Xue Za Zhi. 2009 Sep;38(9):590-3.

Abstract

OBJECTIVE

To study the clinicopathologic features, immunophenotype, differential diagnosis and prognosis of uterine epithelioid trophoblastic tumor(ETT).

METHODS

From 2000 to 2007, 5 ETTs cases were diagnosed in the affiliated Women's Hospital, School of Medicine, Zhejiang University. The pathologic characteristics and immunophenotype of the tumors were analyzed by histological examination and immunohistochemistry of CK18, p63, inhibin-alpha, HCG, HPL, PLAP and Ki-67. The clinical prognostic factors were evaluated based on a following-up data with a period of 11 - 50 months.

RESULTS

The overall prevalence of ETT was 0.48% among all the gestational trophoblastic diseases patients received in the same period. Five ETT patients were in the reproductive ages with a median of 33 years. Histologically, the tumor showed an invasive, nodular growth consisting of uniform mononuclear trophoblastic cells. There were zones of hyaline material in the tumour nests. Necrosis was commonly seen with a characteristic geographic pattern. Immunohistochemically, all cases displayed a diffuse CK18 and p63 positivity, to be either positive focally or negative for HCG, HPL and PLAP staining. Inhibin-alpha staining was positive or negative either in the 5 cases. Two patients died of the tumour relapse: one died after 1 year with the tumor having a high mitotic activity (averagely 15 mitotic figures per 10 high-power fields), and the other died of lung metastasis 2 years after the diagnosis.

CONCLUSIONS

ETT is a rare trophoblastic disease with distinct clinicopathological features and immunostaining patterns. A high mitotic index and lung metastasis are indicators for an unfavorable prognosis.

摘要

目的

研究子宫上皮样滋养细胞肿瘤(ETT)的临床病理特征、免疫表型、鉴别诊断及预后。

方法

2000年至2007年,浙江大学医学院附属妇产科医院诊断出5例ETT病例。通过组织学检查及CK18、p63、抑制素-α、人绒毛膜促性腺激素(HCG)、人胎盘催乳素(HPL)、胎盘碱性磷酸酶(PLAP)和Ki-67的免疫组化分析肿瘤的病理特征和免疫表型。根据11至50个月的随访数据评估临床预后因素。

结果

同期所有妊娠滋养细胞疾病患者中ETT的总体患病率为0.48%。5例ETT患者均处于生育年龄,中位年龄为33岁。组织学上,肿瘤呈浸润性结节状生长,由均匀的单核滋养细胞组成。肿瘤巢内有透明物质区。常见坏死,呈特征性的地图样。免疫组化方面,所有病例CK18和p63弥漫性阳性,HCG、HPL和PLAP染色局灶性阳性或阴性。5例中抑制素-α染色阳性或阴性。2例患者死于肿瘤复发:1例在1年后死亡,肿瘤有高有丝分裂活性(平均每10个高倍视野15个有丝分裂象),另1例在诊断后2年死于肺转移。

结论

ETT是一种罕见的滋养细胞疾病,具有独特的临床病理特征和免疫染色模式。高有丝分裂指数和肺转移是预后不良的指标。

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