Eagles N, Sebire N J, Short D, Savage P M, Seckl M J, Fisher R A
Trophoblastic Tumour Screening & Treatment Centre, Imperial College Healthcare NHS Trust, Charing Cross Campus, Fulham Palace Road, London W6 8RF, UK.
Trophoblastic Tumour Screening & Treatment Centre, Imperial College Healthcare NHS Trust, Charing Cross Campus, Fulham Palace Road, London W6 8RF, UK Department of Paediatric Laboratory Medicine, UCL Institute of Child Health, London WC1N 3JH, UK.
Hum Reprod. 2015 Sep;30(9):2055-63. doi: 10.1093/humrep/dev169. Epub 2015 Jul 22.
What is the risk of further molar pregnancies for women with one or more hydatidiform moles (HM) in relation to molar subtype.
Women with a complete hydatidiform mole (CM) have a 1 in 100 and 1 in 4 risk of further CM after one or two consecutive CM, respectively, while women with a partial hydatidiform mole (PM) have only a small increase in risk for further molar pregnancies.
Women with a molar pregnancy have an increased risk of further HM. A small subgroup of women with recurrent HM has an autosomal recessive condition, familial recurrent hydatidiform moles (FRHM), that predisposes them to molar pregnancies.
STUDY DESIGN, SIZE, DURATION: A retrospective study of subsequent pregnancies in 16 000 women registered at a centralized referral centre, with a CM or PM, between 1990 and 2009.
PARTICIPANTS/MATERIALS, SETTING, METHODS: One hundred and sixty-six women with two or more molar pregnancies were identified from electronic records and patient notes. Histopathological features of all molar tissue were reviewed in these cases and genotyping performed where diagnosis was not possible on the basis of histopathological features alone. In addition, genotyping of molar tissue was performed in all cases of women with three or more CM to establish whether the tissue was diploid and biparental or androgenetic.
This study confirms an increased recurrence risk of ∼1% for a second molar pregnancy and in addition that this risk is associated with CM rather than PM. The data further indicate that the risk of a third HM is associated almost exclusively with CM and enabled an estimate that 1 in 640 women registered with a CM has the rare condition FRHM. The study also found that there was no significant difference between the risk of developing gestational trophoblastic neoplasia (GTN) for typical sporadic CM and the diploid biparental CM associated with FRHM (GTN; proportion difference 0.05, Z = 0.87, P = 0.29).
LIMITATIONS, REASONS FOR CAUTION: While pathology was reviewed for all women with two or more molar pregnancies, not all cases registered underwent central review particularly those women registered in the early 1990s. It is therefore possible that the total number of CM and PM may differ slightly from that stated. While women were followed for a minimum of 5 years, it is possible that some women may subsequently have further molar pregnancies that will not have been included in the present study.
This is the largest study to date on recurrence for molar pregnancies, and as such provides the most detailed information so far regarding the risk of further molar pregnancies for women with a PM or CM. Furthermore, the data provide new insights into the incidence of the rare autosomal recessive condition, FRHM, important information for counselling women with molar pregnancies.
STUDY FUNDING/COMPETING INTERESTS: No competing interests declared. No funding was obtained for this study.
对于有一次或多次葡萄胎(HM)的女性,与葡萄胎亚型相关的再次发生葡萄胎妊娠的风险是多少?
完全性葡萄胎(CM)女性在连续发生一次或两次CM后,再次发生CM的风险分别为1/100和1/4,而部分性葡萄胎(PM)女性再次发生葡萄胎妊娠的风险仅略有增加。
葡萄胎妊娠女性再次发生HM的风险增加。一小部分复发性HM女性患有常染色体隐性疾病,即家族性复发性葡萄胎(FRHM),这使她们易患葡萄胎妊娠。
研究设计、规模、持续时间:对1990年至2009年在一个集中转诊中心登记的16000名患有CM或PM的女性的后续妊娠进行回顾性研究。
参与者/材料、地点、方法:从电子记录和患者病历中识别出166名有两次或更多次葡萄胎妊娠的女性。对所有这些病例中所有葡萄胎组织的组织病理学特征进行了复查,并在仅根据组织病理学特征无法确诊的情况下进行了基因分型。此外,对所有有三次或更多次CM的女性病例的葡萄胎组织进行了基因分型,以确定组织是二倍体且双亲来源还是雄激素来源。
本研究证实第二次葡萄胎妊娠的复发风险增加约1%,此外,这种风险与CM而非PM相关。数据进一步表明第三次HM的风险几乎完全与CM相关,并得出估计,每640名登记有CM的女性中有1人患有罕见的FRHM疾病。该研究还发现,典型散发性CM与与FRHM相关的二倍体双亲CM发生妊娠滋养细胞肿瘤(GTN)的风险之间没有显著差异(GTN;比例差异0.05,Z = 0.87,P = 0.29)。
局限性、谨慎原因:虽然对所有有两次或更多次葡萄胎妊娠的女性进行了病理复查,但并非所有登记病例都经过了中心复查,特别是那些在20世纪90年代初登记的女性。因此,CM和PM的总数可能与所述数字略有不同。虽然对女性进行了至少5年的随访,但可能有一些女性随后会发生更多次葡萄胎妊娠,而这些妊娠未被纳入本研究。
这是迄今为止关于葡萄胎妊娠复发的最大规模研究,因此提供了迄今为止关于PM或CM女性再次发生葡萄胎妊娠风险的最详细信息。此外,数据为罕见常染色体隐性疾病FRHM的发病率提供了新的见解,这是为葡萄胎妊娠女性提供咨询的重要信息。
研究资金/利益冲突:未声明利益冲突。本研究未获得资金。