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妊娠性绒毛膜癌伴肾和肺转移,无原发性子宫起源。

Gestational choriocarcinoma with renal and pulmonary metastases lacking a primary uterine origin.

作者信息

Li Hao-Ming, Hou Wen-Chien, Lai Yu-Ju, Kao Chien-Chang, Chao Tai-Kuang, Yu Mu-Hsien, Su Her-Young

机构信息

Department of General Medicine, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan.

Department of Obstetrics and Gynecology, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan.

出版信息

Taiwan J Obstet Gynecol. 2016 Dec;55(6):881-885. doi: 10.1016/j.tjog.2015.08.028.

DOI:10.1016/j.tjog.2015.08.028
PMID:28040140
Abstract

OBJECTIVE

We describe a case of gestational choriocarcinoma metastasized to the kidney and lung, which presented initially as refractory hematuria after a term pregnancy 5 years earlier.

CASE REPORT

A 35-year-old woman, G2P1, with a previous history of full-term pregnancy in 2009, presented to the emergency department complaining of intermittent gross hematuria for 2 months. Abdominal computed tomography showed a suspicious arteriovenous malformation in the right kidney and a thrombus within the right renal vein. Transarterial embolization was performed twice to treat the refractory hematuria but was unsuccessful, and radical nephrectomy of the right kidney was performed. The diagnosis was gestational metastatic choriocarcinoma of the kidney based on morphological, immunohistochemical, and DNA studies. Lung metastases were found by computed tomography of the chest. Pelvic ultrasound was performed but showed no primary tumor in the uterine cavity. After surgical intervention, adjuvant chemotherapy involving first single-agent chemotherapy with methotrexate followed by multiagent chemotherapy (EMACO regimen) failed.

CONCLUSION

In women of reproductive age, unexplained hematuria should raise concerns about possible choriocarcinoma, either metastatic gestational or primary nongestational choriocarcinoma of the kidney.

摘要

目的

我们描述一例妊娠性绒毛膜癌转移至肾脏和肺的病例,该病例最初表现为5年前足月妊娠后出现的难治性血尿。

病例报告

一名35岁女性,孕2产1,既往有2009年足月妊娠史,因间歇性肉眼血尿2个月就诊于急诊科。腹部计算机断层扫描显示右肾有可疑动静脉畸形,右肾静脉内有血栓形成。为治疗难治性血尿进行了两次经动脉栓塞,但均未成功,遂行右肾根治性切除术。根据形态学、免疫组织化学和DNA研究,诊断为肾脏妊娠转移性绒毛膜癌。胸部计算机断层扫描发现肺部转移。进行了盆腔超声检查,但未发现宫腔内有原发性肿瘤。手术干预后,辅助化疗最初采用甲氨蝶呤单药化疗,随后采用多药化疗(EMACO方案),但均失败。

结论

在育龄女性中,不明原因的血尿应引起对可能的绒毛膜癌的关注,无论是转移性妊娠性绒毛膜癌还是原发性非妊娠性肾脏绒毛膜癌。

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