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山东大学学报 (医学版) ›› 2018, Vol. 56 ›› Issue (5): 64-69.doi: 10.6040/j.issn.1671-7554.0.2018.313

• 基础医学 • 上一篇    下一篇

子宫腺肉瘤15例临床病例分析

夏雪薇,张贵宇,王立杰,张爱荣,王国云,姜洁,张师前,张辉,王文霞,崔保霞   

  1. 山东大学齐鲁医院妇产科, 山东 济南 250012
  • 收稿日期:2018-03-12 发布日期:2022-09-27
  • 通讯作者: 崔保霞. E-mail:cuibaoxia@sdu.edu.cn
  • 基金资助:
    国家重点研发计划(2016YFC1302900)

Uterine adenosarcoma: a study of 15 cases

XIA Xuewei, ZHANG Guiyu, WANG Lijie, ZHANG Airong, WANG Guoyun, JIANG Jie, ZHANG Shiqian, ZHANG Hui, WANG Wenxia, CUI Baoxia   

  1. Department of Obstetrics and Gynecology, Qilu Hospital of Shandong University, Jinan 250012, Shandong, China
  • Received:2018-03-12 Published:2022-09-27

摘要: 目的 探讨子宫腺肉瘤(UA)患者的临床症状、诊断及治疗。 方法 回顾性分析2009年10月至2017年10月收治并病理确诊的15例UA患者临床资料,进行随访观察,并对相关文献进行复习。 结果 15例患者主要临床症状为阴道不规则流血(12例,占80%)、下腹部疼痛、宫颈口脱出肿物等。其中宫颈腺肉瘤5例,伴肉瘤过度生长2例。根据2009年国际妇产科联盟(FIGO)分期标准:子宫颈腺肉瘤5例,其中ⅠB1期4例、ⅣB期1例;子宫体腺肉瘤10例,其中ⅠA期2例、ⅠB期4例、ⅠC期1例、ⅡA期1例、ⅢB期1例、ⅢC期1例。全部病例均行手术治疗,13例术后辅以化疗。随访4例因疾病进展死亡,1例因化疗后出现肺栓塞死亡,10例无进展生存。 结论 UA是一种发病率较低的子宫肉瘤,患者症状、体征无特异性,易被误诊,常由术后病理检查及免疫组织化学确诊。该病常见于绝经后妇女,但也可见于年轻女性。虽然为低度恶性肿瘤,也应详细评估术后复发风险,尤其是合并肉瘤过度生长、深肌层浸润及伴有异源性分化的患者预后差。

关键词: 子宫腺肉瘤, 诊断, 治疗, 预后

Abstract: Objective To investigate the clinical symptoms, diagnosis and treatment of uterine adenosarcoma(UA). Methods The clinical data of 15 UA patients treated during Oct. 2009 and Oct. 2017 were retrospectively analyzed and related literatures were reviewed. Results Irregular vaginal bleeding was observed in 80% of cases. The other symptoms included lower abdominal pain, cervical spondylolysis and so on. The adenosarcoma was located on the cervix in 5 cases and 2 of them had sarcoma overgrowth. According to the FIGO stage(2009), of the 5 cervical adenosarcoma cases, 4 were ⅠB1, and 1 was ⅣB. Of the 10 uterine body adenosarcoma, 2 were ⅠA, 4 were ⅠB, and other 4 were ⅠC, ⅡA, ⅢB and ⅢC respectively. All 15 cases underwent surgical treatment, and 13 of them were treated with chemotherapy. During the follow-up, 4 patients died of disease progression, 1 died of pulmonary embolism after chemotherapy, and 10 survived progression-free. Conclusion UA is a rare disease. As the symptoms and signs are nonspecific, it can easily be misdiagnosed. Therefore, it needs to be differentiated from other benign and malignant lesions, and confirmed by postoperative pathological and immunohistochemical examinations. The disease generally occurs in postmenopausal women, but can also be found in young women. Although it is not malignant, the risk of postoperative recurrence should be evaluated carefully, especially in patients with sarcoma overgrowth, deep myometrial invasion and heterogenous differentiation.

Key words: Uterine adenosarcoma, Diagnosis, Treatment, Prognosis

中图分类号: 

  • R737.33
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