Chen R J, Huang S C, Chow S N, Hsieh C Y, Hsu H C
Department of Obstetrics and Gynecology, National Taiwan University Hospital, Taipei.
Br J Obstet Gynaecol. 1994 Apr;101(4):330-4. doi: 10.1111/j.1471-0528.1994.tb13620.x.
A 16 year review of persistent gestational trophoblastic tumour when the antecedent pregnancy was a partial hydatidiform mole.
Cases of persistent gestational trophoblastic tumour with partial hydatidiform mole as the antecedent pregnancy were reviewed for the period 1976 to 1992. DNA ploidy was analysed by flow cytometry.
A University Hospital which is a reference centre for gestational trophoblastic tumour.
The case notes of 207 women with persistent gestational trophoblastic tumour were reviewed.
A rise (or failure to fall) of beta hCG titre, or sign of metastasis.
Six (2.9%) women had partial hydatidiform mole as the antecedent pregnancy and all were initially judged to be low risk. However, two developed pulmonary metastasis; one woman developed persistent gestational trophoblastic tumour shortly after a hysterotomy, and none developed choriocarcinoma. The geometric mean of serum beta hCG concentrations at the initiation of chemotherapy was 868 mIU/ml (95% CI 114-1524). Of the six women, one achieved remission after total abdominal hysterectomy, and five after chemotherapy. The mean interval from starting treatment to remission was 68 days (95% CI 27.9-108.0). The initial beta hCG titre and interval were not statistically different from those found in cases of persistent gestational trophoblastic tumour when the antecedent pregnancy was not partial hydatidiform mole. Of the six, the DNA content was triploid in three and diploid in two. One of the two diploid cases required multiple courses of chemotherapy to achieve remission.
Partial hydatidiform mole can have malignant sequelae and can develop very soon after treatment. Its DNA content can be either diploid or triploid, the lungs being the most common site of metastasis. After evacuation of partial hydatidiform mole, immediate chest X-ray and regular follow up of the serum beta hCG level is necessary.
对以部分性葡萄胎为前次妊娠的持续性妊娠滋养细胞肿瘤进行16年回顾性研究。
回顾1976年至1992年期间以部分性葡萄胎为前次妊娠的持续性妊娠滋养细胞肿瘤病例。采用流式细胞术分析DNA倍体。
一家作为妊娠滋养细胞肿瘤参考中心的大学医院。
回顾207例持续性妊娠滋养细胞肿瘤患者的病历。
β-hCG水平升高(或未下降)或转移迹象。
6例(2.9%)患者前次妊娠为部分性葡萄胎,所有患者最初均被判定为低危。然而,2例发生肺转移;1例患者在子宫切除术后不久发生持续性妊娠滋养细胞肿瘤,无一例发生绒毛膜癌。化疗开始时血清β-hCG浓度的几何平均值为868 mIU/ml(95%可信区间114 - 1524)。6例患者中,1例在全腹子宫切除术后缓解,5例在化疗后缓解。从开始治疗到缓解的平均间隔时间为68天(95%可信区间27.9 - 108.0)。初始β-hCG水平和间隔时间与前次妊娠非部分性葡萄胎的持续性妊娠滋养细胞肿瘤病例相比,差异无统计学意义。6例中,3例DNA含量为三倍体,2例为二倍体。2例二倍体病例中有1例需要多疗程化疗才能缓解。
部分性葡萄胎可产生恶性后遗症,且可在治疗后很快发生。其DNA含量可为二倍体或三倍体,肺是最常见的转移部位。部分性葡萄胎清宫术后,需立即进行胸部X线检查并定期监测血清β-hCG水平。