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肿瘤标志物在卵巢良性肿块鉴别诊断中的应用

Tumor Markers in Differential Diagnosis of Benign Ovarian Masses.

作者信息

Li Tianlong, Hou Nana, Mao Lili, Liu Fangmei, Ma Zilong, Wang Li, Xu Xiyue, Yan Guanghui, Han Yujia, Wei Jinxian

机构信息

Department of Gynecology, Zhengzhou First People's Hospital, Zhengzhou, People's Republic of China.

出版信息

Int J Womens Health. 2024 Sep 16;16:1517-1531. doi: 10.2147/IJWH.S471058. eCollection 2024.

DOI:10.2147/IJWH.S471058
PMID:39309199
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11414758/
Abstract

BACKGROUND

Although there are many benign tumors in the ovarian adnexal area, the four most common types are still luteal cyst, ovarian mature cystic teratoma (OMCT), ovarian endometriosis, and benign epithelial tumors of the ovary.

PURPOSE

This study aimed to examine the correlation between six tumor markers (CEA, AFP, CA125, CA19-9, SCC, HE4) in the differential diagnosis of female adnexal benign masses and assess their diagnostic value.

PATIENTS AND METHODS

In this study, 135 patients with adnexal benign masses were treated in Zhengzhou first people's Hospital from January 2018 to January 2023. 135 patients were divided into four groups: luteal cyst (13.3%), OMCT (42.2%), ovarian endometriosis (23.7%) and benign epithelial tumors of the ovary (including mucinous cystadenoma and serous cystadenoma) in group D. The receiver-operating characteristic (ROC) curve was used to assess the diagnostic value of each marker and combined detection.

RESULTS

The diameter of luteal cysts was significantly smaller than that of benign ovarian tumors (p < 0.001). ROC analysis showed that the combination of AFP, CA125, CA19-9, and SCC had a higher diagnostic rate for luteal cysts (AUC=0.871; sensitivity: 71.8%; specificity: 88.9). The SCC level in OMCT was significantly higher than in other benign ovarian tumors (p=0.007). ROC analysis indicated that the combination of AFP, HE4, and SCC had a higher diagnostic rate for OMCT (AUC=0.753; sensitivity: 65.4%; specificity: 75.4%). The CA125 level in ovarian endometriosis was significantly higher than in other accessory benign tumors (p < 0.001). ROC analysis demonstrated that the combination of AFP, CA125, and CA19-9 had a higher diagnostic rate for ovarian endometriosis (AUC=0.935; sensitivity: 76.7%; specificity: 96.9%). The tumor diameter of benign epithelial tumors of the ovary was significantly larger than that of other benign ovarian tumors (p < 0.001). ROC analysis revealed that the combination of CA125 and CA19-9 had a higher diagnostic rate for benign epithelial tumors of the ovary (AUC=0.792; sensitivity: 64.5%; specificity: 85.7%).

CONCLUSION

The findings of this study demonstrate that the combined use of tumor markers (CEA, AFP, CA125, CA19-9, SCC, and HE4) has value in diagnosing benign ovarian tumors, including luteal cysts, OMCT, ovarian endometriosis, and benign epithelial tumors of the ovary. However, it is important to acknowledge the limitations of this study, which include its single-center nature and the small sample size. Despite these limitations, the results highlight the potential utility of these markers in clinical practice.

摘要

背景

尽管卵巢附件区存在多种良性肿瘤,但最常见的四种类型仍是黄体囊肿、卵巢成熟囊性畸胎瘤(OMCT)、卵巢子宫内膜异位症和卵巢良性上皮性肿瘤。

目的

本研究旨在探讨六种肿瘤标志物(癌胚抗原、甲胎蛋白、糖类抗原125、糖类抗原19-9、鳞状细胞癌抗原、人附睾蛋白4)在女性附件区良性肿块鉴别诊断中的相关性,并评估其诊断价值。

患者与方法

本研究纳入了2018年1月至2023年1月在郑州市第一人民医院接受治疗的135例附件区良性肿块患者。135例患者被分为四组:黄体囊肿组(13.3%)、OMCT组(42.2%)、卵巢子宫内膜异位症组(23.7%)和D组卵巢良性上皮性肿瘤(包括黏液性囊腺瘤和浆液性囊腺瘤)。采用受试者工作特征(ROC)曲线评估各标志物及联合检测的诊断价值。

结果

黄体囊肿直径显著小于卵巢良性肿瘤(p<0.001)。ROC分析显示,甲胎蛋白、糖类抗原125、糖类抗原19-9和鳞状细胞癌抗原联合检测对黄体囊肿的诊断率较高(曲线下面积=0.871;灵敏度:71.8%;特异度:88.9%)。OMCT中鳞状细胞癌抗原水平显著高于其他卵巢良性肿瘤(p=0.007)。ROC分析表明,甲胎蛋白、人附睾蛋白4和鳞状细胞癌抗原联合检测对OMCT的诊断率较高(曲线下面积=0.753;灵敏度:6

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5712/11414758/30bd0bc42da9/IJWH-16-1517-g0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5712/11414758/da3b75d6f467/IJWH-16-1517-g0001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5712/11414758/e6e1cbb856ac/IJWH-16-1517-g0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5712/11414758/30bd0bc42da9/IJWH-16-1517-g0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5712/11414758/da3b75d6f467/IJWH-16-1517-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5712/11414758/3005c38d0ce2/IJWH-16-1517-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5712/11414758/01218d2c611c/IJWH-16-1517-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5712/11414758/2b4347af1e53/IJWH-16-1517-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5712/11414758/ad19c42731ca/IJWH-16-1517-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5712/11414758/a82235e6ee7d/IJWH-16-1517-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5712/11414758/e6e1cbb856ac/IJWH-16-1517-g0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5712/11414758/30bd0bc42da9/IJWH-16-1517-g0008.jpg

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