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妊娠合并黄素化囊肿:一例报告并文献复习

Hyperreactio luteinalis associated with pregnancy: a case report and review of the literature.

作者信息

Schnorr J A, Miller H, Davis J R, Hatch K, Seeds J

机构信息

Department of Obstetrics and Gynecology, University of Virginia Health Sciences Center, Charlottesville 22908, USA.

出版信息

Am J Perinatol. 1996 Feb;13(2):95-7. doi: 10.1055/s-2007-994300.

DOI:10.1055/s-2007-994300
PMID:8672193
Abstract

Hyperreactio luteinalis is a condition associated with bilateral and, in rare cases, unilateral ovarian enlargement due to theca lutein cysts. Hyperreactio luteinalis is a benign condition, usually found incidentally at cesarean section, which can appear anaplastic and lead to unnecessary ovarian resection. A 21-year-old Hispanic woman, G2P1, presented at 19 weeks with a singleton pregnancy, bilaterally enlarged ovaries, and a normal beta hCG. Over the next four months, her ovaries increased 75% in size with the right ovary becoming entrapped in the pelvis. The patient underwent a primary low transverse cesarean section. The ovaries had an anaplastic appearance and on frozen section revealed multiple benign theca lutein cysts. There are 51 reported cases of hyperreactio luteinalis associated with a normal pregnancy in the literature. It is estimated that approximately 60% of the cases of hyperreactio luteinalis unassociated with trophoblastic disease occur with normal singleton pregnancy. There are multiple benign ovarian lesions including hyperreactio luteinalis that can mimic ovarian neoplasms. Accordingly, it is important to exclude these from the differential diagnosis via a wedge biopsy and frozen section to avoid unnecessary surgical excision.

摘要

卵巢黄素化囊肿过度反应是一种与双侧卵巢增大相关的病症,在罕见情况下也可单侧卵巢增大,由黄素囊肿引起。卵巢黄素化囊肿过度反应是一种良性病症,通常在剖宫产时偶然发现,其外观可能呈间变,导致不必要的卵巢切除。一名21岁的西班牙裔女性,孕2产1,孕19周时因单胎妊娠、双侧卵巢增大且β-人绒毛膜促性腺激素正常前来就诊。在接下来的四个月里,她的卵巢大小增加了75%,右侧卵巢被困于盆腔。患者接受了低位横切口剖宫产术。卵巢外观呈间变,冰冻切片显示多个良性黄素囊肿。文献中报道了51例与正常妊娠相关的卵巢黄素化囊肿过度反应病例。据估计,约60%与滋养细胞疾病无关的卵巢黄素化囊肿过度反应病例发生于正常单胎妊娠。包括卵巢黄素化囊肿过度反应在内的多种良性卵巢病变可酷似卵巢肿瘤。因此,通过楔形活检和冰冻切片从鉴别诊断中排除这些病变以避免不必要的手术切除很重要。

相似文献

1
Hyperreactio luteinalis associated with pregnancy: a case report and review of the literature.妊娠合并黄素化囊肿:一例报告并文献复习
Am J Perinatol. 1996 Feb;13(2):95-7. doi: 10.1055/s-2007-994300.
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Severe preeclampsia and fetal virilization in a spontaneous singleton pregnancy complicated by hyperreactio luteinalis.自发性单胎妊娠合并妊娠黄体反应过度导致严重子痫前期和胎儿男性化。
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Bilateral theca lutein cysts: a rare cause of acute abdomen in pregnancy.双侧卵泡膜黄素囊肿:妊娠期急腹症的罕见病因。
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Hirsutism and hyperandrogenism associated with hyperreactio luteinalis in a singleton pregnancy: a case report.单胎妊娠中与黄素化卵泡膜细胞增生症相关的多毛症和高雄激素血症:一例报告
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Hyperreactio luteinalis in a normal singleton pregnancy. A case report.正常单胎妊娠中的黄素化过度反应。病例报告。
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Int J Gynecol Pathol. 2021 Sep 1;40(5):427-434. doi: 10.1097/PGP.0000000000000746.

引用本文的文献

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Unrecognized Primary Hypothyroidism As a Possible Cause of Hyperreactio Luteinalis.未被识别的原发性甲状腺功能减退症作为黄体期过度反应的可能原因。
Cureus. 2021 Feb 26;13(2):e13573. doi: 10.7759/cureus.13573.
2
Testosterone serum levels are not predictive of maternal virilization in hyperreactio luteinalis.血清睾酮水平不能预测黄体反应过度中的母体男性化。
Arch Gynecol Obstet. 2021 Jan;303(1):129-134. doi: 10.1007/s00404-020-05745-6. Epub 2020 Aug 19.
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Hyperreactio luteinalis and hypothyroidism: A case report.黄素化反应亢进与甲状腺功能减退:一例报告。
Case Rep Womens Health. 2018 Dec 29;21:e00094. doi: 10.1016/j.crwh.2018.e00094. eCollection 2019 Jan.
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Clitoral epidermoid cyst presenting as pseudoclitoromegaly of pregnancy.表现为妊娠期间假性阴蒂肥大的阴蒂表皮样囊肿。
AJP Rep. 2013 May;3(1):57-62. doi: 10.1055/s-0033-1334461. Epub 2013 Feb 7.
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Hyperreactio luteinalis with preeclampsia.黄素化囊肿合并子痫前期
J Emerg Trauma Shock. 2010 Jul;3(3):298. doi: 10.4103/0974-2700.66545.
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Ovarian hyperstimulation syndrome complicating a spontaneous singleton pregnancy: a case report.卵巢过度刺激综合征并发自然单胎妊娠:一例报告
J Assist Reprod Genet. 2001 Feb;18(2):120-3. doi: 10.1023/a:1026543027300.