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妊娠合并无性细胞瘤。

Dysgerminoma associated with pregnancy.

作者信息

Karlen J R, Akbari A, Cook W A

出版信息

Obstet Gynecol. 1979 Mar;53(3):330-5.

PMID:424104
Abstract

From a review of 26 reported case (our case being the 27th) of dysgerminoma associated with pregnancy, several salient facts are evident. Torsion and incarceration are common among these rapidly enlarging tumors. Obstetrical complications occurred in nearly half and fetal demise in one quarter of the reviewed cases. Our case was typical of patients presenting with this vexed problems: The patient was under 25 (as were 70%); nulliparous (as were 67%); and the tumor appeared confined to one ovary (as in 89%). Authorities are in dispute as to the treatment of stage IA dysgerminomas, and the association of pregnancy complicates this debate even further. The results of conservative treatment in this series were jarring: There were recurrences in 30% of the 23 stage IA tumors, and the recurrences were all following unilateral oophorectomy. In our case, the grossly normal contralateral ovary was infiltrated with dysgerminoma cells. While treatment of a young woman with a dysgerminoma of 1 ovary is a matter of perplexity, we believe that a unilateral operation should be limited to those women who desire above all earthly things to retain their childbearing capacity.

摘要

回顾26例(我们的病例为第27例)妊娠合并无性细胞瘤的报道后,一些显著事实显而易见。在这些迅速增大的肿瘤中,扭转和嵌顿很常见。近一半病例出现产科并发症,四分之一的病例出现胎儿死亡。我们的病例是这类棘手问题患者的典型代表:患者年龄在25岁以下(70%的患者如此);未生育(67%的患者如此);肿瘤似乎局限于一侧卵巢(89%的病例如此)。对于IA期无性细胞瘤的治疗,权威们存在争议,而妊娠的合并使这场争论更加复杂。该系列保守治疗的结果令人震惊:23例IA期肿瘤中有30%复发,且复发均发生在单侧卵巢切除术后。在我们的病例中,肉眼看似正常的对侧卵巢被无性细胞瘤细胞浸润。虽然治疗单侧卵巢无性细胞瘤的年轻女性是个难题,但我们认为,单侧手术应仅限于那些最渴望保留生育能力的女性。

相似文献

1
Dysgerminoma associated with pregnancy.妊娠合并无性细胞瘤。
Obstet Gynecol. 1979 Mar;53(3):330-5.
2
[Dysgerminoma of the ovary during pregnancy (author's transl)].妊娠期卵巢无性细胞瘤(作者译)
Wien Klin Wochenschr. 1977 Oct 14;89(19):652-4.
3
Pregnancy outcomes and menstrual function after fertility sparing surgery for pure ovarian dysgerminomas.纯卵巢无性细胞瘤保留生育功能手术后的妊娠结局及月经功能
Arch Gynecol Obstet. 2005 Feb;271(2):104-8. doi: 10.1007/s00404-004-0601-6. Epub 2004 Mar 9.
4
Pregnancy in a woman with a Y chromosome after removal of an ovarian dysgerminoma.一名患有Y染色体的女性在切除卵巢无性细胞瘤后怀孕。
Gynecol Oncol. 2000 Dec;79(3):519-21. doi: 10.1006/gyno.2000.6004.
5
[Ovarian seminoma and pregnancy. Apropos of a new case].[卵巢精原细胞瘤与妊娠。附1例新病例]
J Gynecol Obstet Biol Reprod (Paris). 1989;18(4):487-91.
6
[Treatment of pure stage one ovarian dysgerminoma in young women. Report of a case and review of the literature].
Minerva Ginecol. 1999 Jan-Feb;51(1-2):27-30.
7
[Dysgerminoma of the ovary. Presentation of case report].[卵巢无性细胞瘤。病例报告展示]
Akush Ginekol (Sofiia). 2013;52(2):56-9.
8
[Characteristics of rare ovarian tumors--possibilities of organ preservation].[罕见卵巢肿瘤的特征——保留器官的可能性]
Zentralbl Gynakol. 1996;118(6):322-5.
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Late relapse of ovarian dysgerminoma: case report and literature review.卵巢无性细胞瘤晚期复发:病例报告及文献综述
Gynecol Oncol. 1999 Jan;72(1):111-2. doi: 10.1006/gyno.1998.5207.
10
[Results of fertility preserving operations in malignant ovarian tumors].[恶性卵巢肿瘤保留生育功能手术的结果]
Zentralbl Gynakol. 1996;118(6):317-21.

引用本文的文献

1
Ovarian dysgerminoma in pregnancy: A case report.妊娠合并卵巢未成熟畸胎瘤 1 例报告。
Medicine (Baltimore). 2021 Apr 9;100(14):e25364. doi: 10.1097/MD.0000000000025364.
2
Pregnancy with giant ovarian dysgerminoma: A case report and literature review.妊娠合并巨大卵巢无性细胞瘤:1例报告及文献复习
Medicine (Baltimore). 2020 Oct 9;99(41):e21214. doi: 10.1097/MD.0000000000021214.
3
Ovarian dysgerminoma in pregnancy: A case report and literature review.妊娠性卵巢未成熟畸胎瘤:病例报告及文献复习。
Cancer Biol Ther. 2018 Aug 3;19(8):649-658. doi: 10.1080/15384047.2018.1450118. Epub 2018 Apr 25.
4
An Incidental Finding of Bilateral Dysgerminoma During Cesarean Section: Dilemmas in Management.剖宫产术中偶然发现双侧无性细胞瘤:治疗困境
J Clin Diagn Res. 2016 Aug;10(8):QD04-5. doi: 10.7860/JCDR/2016/20163.8319. Epub 2016 Aug 1.
5
Ovarian carcinoma associated with pregnancy: a clinicopathologic analysis of 23 cases and review of the literature.妊娠合并卵巢癌:23例临床病理分析及文献复习
BMC Pregnancy Childbirth. 2008 Jan 20;8:3. doi: 10.1186/1471-2393-8-3.