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Hyperreactio luteinalis in a monochorionic twin pregnancy complicated by preeclampsia: A case report

机译:黄体超反应性在单绒毛膜双胎妊娠合并先兆子痫中的病例报告

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摘要

Hyperreactio luteinalis (HL) is a rare benign complication of pregnancy that is characterized by progressive ovarian enlargement and hyperandrogenism. We present a case of a 30-year-old woman with a spontaneous monochorionic diamniotic twin pregnancy who presented with early-onset preeclampsia, concern about possible twin-twin transfusion syndrome, and bilateral enlarged ovarian masses. Both ovaries had multiple thin-walled unilocular cysts; one ovary measured 17.9 × 17.5 × 9.1 cm and the other 12.5 × 11 × 12.3 cm. After extensive counseling, the patient underwent an uncomplicated dilation and evacuation. Postoperative assessment indicated elevated androgen levels, which spontaneously resolved, supporting the clinical diagnosis of HL. It is important to consider HL in the differential diagnosis of adnexal masses in pregnancy. HL spontaneously regresses after delivery and is managed expectantly. HL has been associated with gestational trophoblastic disease, multiple gestations, preeclampsia, and twin-twin transfusion syndrome.
机译:黄体反应亢进症(HL)是一种罕见的良性妊娠并发症,其特征是进行性卵巢增大和雄激素过多。我们介绍了一个患有自发性单绒毛膜羊膜炎双胎妊娠的30岁妇女,该病例表现为先发性先兆子痫,对可能的双胎输血综合征的关注以及双侧卵巢肿大。两个卵巢均具有多个薄壁单眼囊肿。一个子房为17.9×17.5×9.1 cm,另一个为12.5×11×12.3 cm。经过广泛的咨询,患者经历了简单的扩张和撤离。术后评估表明雄激素水平升高,可自发解决,支持HL的临床诊断。在孕期附件包块的鉴别诊断中考虑HL很重要。 HL在分娩后自发消退并得到预期的管理。 HL与妊娠滋养细胞疾病,多胎妊娠,先兆子痫和双胎输血综合征有关。

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