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葡萄胎

Hydatidiform Mole

作者信息

Cue Lauren, Farci Fabiola, Ghassemzadeh Sassan, Kang Michael

机构信息

Jersey City Medical Center, Rutgers Barnabas Health

Pisa University

Abstract

A hydatidiform mole, commonly referred to as a molar pregnancy, is a rare abnormality in pregnancy classified under gestational trophoblastic diseases (GTD), which stem from the placenta and may metastasize. Hydatidiform moles are characterized by abnormal fertilization, resulting in villous hydrops and trophoblastic hyperplasia with or without embryonic development. Other forms of GTD include gestational choriocarcinoma—which can be aggressively malignant and invasive—and placental site trophoblastic tumors. Please see StatPearls' companion reference, "Gestational Trophoblastic Disease," for more information. Although described as early as Hippocrates’ era, who explained their formation through the consumption of dirty water by pregnant women, the condition was more accurately characterized in 1752 by William Smelie, who likened its appearance to a “bunch of grapes,” a hallmark feature of molar pregnancies resulting from swollen, hydropic villi. Hydatidiform moles are categorized as complete or partial and are usually noninvasive forms of GTD. Overrepresentation of the paternal genome in sporadic hydatidiform moles is a fundamental genetic event leading to overall alteration of imprinting gene expression in the molar trophoblast, being completely androgenetic in complete hydatidiform moles and diandric triploid in partial hydatidiform moles. However, although hydatidiform moles are considered benign, they are premalignant lesions and can potentially become malignant and invasive.  Complete molar pregnancies present with symptoms such as first-trimester vaginal bleeding, severe nausea, and high β-human chorionic gonadotropin (β-hCG) levels. Partial moles may present similarly but often resemble a spontaneous abortion and may include detectable fetal heart tones. Both molar types are detectable via ultrasonography, which typically reveals distinct patterns; complete moles demonstrate anechoic cystic clusters (“grape clusters”) and partial moles demonstrate fetal parts. Histopathological examination postevacuation confirms the diagnosis with visualization of characteristic villous changes. Treatment typically involves dilation and curettage (D&C), and hysterectomy may be considered for patients not desiring future pregnancies. Posttreatment, regular β-hCG monitoring is essential to detect potential progression to gestational trophoblastic neoplasia (GTN).

摘要

葡萄胎通常被称为葡萄样妊娠,是妊娠中一种罕见的异常情况,归类于妊娠滋养细胞疾病(GTD),该疾病起源于胎盘且可能发生转移。葡萄胎的特征是受精异常,导致绒毛水肿和滋养细胞增生,可有或无胚胎发育。GTD的其他形式包括妊娠性绒毛膜癌(其具有侵袭性且可能为恶性)和胎盘部位滋养细胞肿瘤。更多信息请参阅StatPearls的配套参考文献《妊娠滋养细胞疾病》。尽管早在希波克拉底时代就对其进行了描述,当时他认为葡萄胎是孕妇饮用脏水所致,但1752年威廉·斯梅利对其进行了更准确的描述,他将其外观比作“一串葡萄”,这是由肿胀、水肿的绒毛导致的葡萄样妊娠的一个标志性特征。葡萄胎分为完全性和部分性,通常是GTD的非侵袭性形式。散发性葡萄胎中父系基因组的过度表达是导致葡萄胎滋养细胞中印迹基因表达整体改变的一个基本遗传事件,完全性葡萄胎完全为雄核发育,部分性葡萄胎为双雄三倍体。然而,尽管葡萄胎被认为是良性的,但它们是癌前病变,有可能发展为恶性且具有侵袭性。完全性葡萄胎妊娠的症状包括孕早期阴道出血、严重恶心和高β-人绒毛膜促性腺激素(β-hCG)水平。部分性葡萄胎可能有类似症状,但通常类似自然流产,可能包括可检测到的胎心音。两种类型的葡萄胎均可通过超声检查发现,超声通常显示出不同的模式;完全性葡萄胎表现为无回声囊性团块(“葡萄串”),部分性葡萄胎表现为胎儿部分。清宫术后的组织病理学检查通过观察特征性的绒毛变化来确诊。治疗通常包括扩张刮宫术(D&C),对于不希望未来怀孕的患者可考虑子宫切除术。治疗后,定期监测β-hCG对于检测是否可能进展为妊娠滋养细胞肿瘤(GTN)至关重要。

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