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妊娠时腹主动脉旁淋巴结子宫内膜异位症:病例报告及文献复习。

Endometriosis in para-aortic lymph nodes during pregnancy: case report and review of literature.

机构信息

Department of Obstetrics and Gynecology, University of Southern California, Los Angeles, California 90033, USA.

出版信息

Fertil Steril. 2011 Jun;95(7):2429.e9-13. doi: 10.1016/j.fertnstert.2011.01.157. Epub 2011 Feb 26.

DOI:10.1016/j.fertnstert.2011.01.157
PMID:21354563
Abstract

OBJECTIVE

To report a case of endometriosis in para-aortic lymph nodes during pregnancy.

DESIGN

Case report.

SETTING

Tertiary care center.

PATIENT(S): A 25-year-old multipara pregnant woman with a history of chronic pelvic pain and ovarian cystectomies for bilateral endometriomas.

INTERVENTION(S): The patient was admitted with a placenta previa and a subchorionic hemorrhage at 24 weeks 5 days' gestation, and subsequently developed uterine contractions. Magnetic resonance imaging revealed a large complex adnexal mass adherent to the uterus and pelvic and para-aortic lymphadenopathy. Tocolysis could not be achieved and the patient underwent cesarean delivery at 26 weeks 3 days. An implant on the uterus and an enlarged para-aortic lymph node were removed surgically at that time.

MAIN OUTCOME MEASURE(S): Involvement of lymph node by endometriosis and presence of a recurrent endometrioma.

RESULT(S): Endometriosis was confirmed pathologically in para-aortic lymph nodes. Uterine serosal biopsy demonstrated endometriosis, and the large adnexal cyst was grossly consistent with endometrioma. The patient delivered a viable male infant at 26 weeks 3 days.

CONCLUSION(S): To our knowledge, this is the first reported case of endometriosis in para-aortic lymph nodes. Its presence supports the hypothesis that endometriosis travels lymphatically, and not simply via locoregional spread. Lymphatic spread also further supports the theory that endometriosis is an aggressive chronic systemic disease.

摘要

目的

报告一例妊娠期间发生在腹主动脉旁淋巴结的子宫内膜异位症病例。

设计

病例报告。

地点

三级医疗中心。

患者

一位 25 岁的多产妇,有慢性盆腔痛病史和因双侧卵巢子宫内膜异位囊肿而行卵巢囊肿切除术病史。

干预措施

患者因胎盘前置和 24 周 5 天妊娠的胎盘下出血入院,随后出现子宫收缩。磁共振成像显示子宫和盆腔及腹主动脉旁有一个大的复杂附件肿块,且与子宫粘连,并有盆腔和腹主动脉旁淋巴结病。宫缩抑制剂治疗无效,患者于 26 周 3 天行剖宫产术。当时手术切除了子宫上的病灶和增大的腹主动脉旁淋巴结。

主要观察指标

淋巴结受累和复发性子宫内膜异位囊肿的存在。

结果

腹主动脉旁淋巴结的子宫内膜异位症得到病理证实。子宫浆膜活检显示有子宫内膜异位症,大的附件囊肿大体上符合子宫内膜异位囊肿。患者于 26 周 3 天分娩出一个存活的男婴。

结论

据我们所知,这是首例腹主动脉旁淋巴结子宫内膜异位症的报告病例。其存在支持了子宫内膜异位症通过淋巴途径传播,而不仅仅是通过局部扩散的假说。淋巴扩散也进一步支持了子宫内膜异位症是一种侵袭性慢性全身疾病的理论。

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Endometriosis in para-aortic lymph node resembling a malignancy: a case report and literature review.
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Endometriosis of para-aortic node masquerading a malignancy: a rare occurrence.腹主动脉旁淋巴结子宫内膜异位症伪装恶性肿瘤:罕见发生。
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