Dandy-Walker syndrome with duplex kidney abnormalities in trisomy 18-A rare case report

被引:2
作者
Wang, Tun-Jun [1 ]
Li, Yi-Ying [2 ]
Wu, Wan-Ju [2 ]
Lin, Chi-Kang [1 ]
Wang, Chun-Kai [1 ]
Wang, Chen-Yu [1 ]
Hwang, Kwei-Shuai [1 ]
Su, Her-Young [1 ]
机构
[1] Triserv Gen Hosp, Dept Obstet & Gynecol, Natl Def Med Ctr, Taipei, Taiwan
[2] Taiji Fetal Med Ctr, Taipei, Taiwan
来源
TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY | 2017年 / 56卷 / 05期
关键词
Edwards syndrome; Dandy-Walker malformation; Trisomy; 18; PRENATAL-DIAGNOSIS; MALFORMATION; MOSAICISM; VARIANT;
D O I
10.1016/j.tjog.2017.08.022
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: Trisomy 18 is one of the major numerical chromosomal disorders. The incidence of trisomy 18 is approximately one in 6000 live births. Dandy Walker malformation (DWM) is the most common congenital malformation of the cerebellum, with an incidence of about one in 5000 live births. The incidence of trisomy 18 associated with DWM is rare and long-term survival rate is very low. Case report: A case involving a 39-year-old pregnant female with a case of trisomy 18 associated with DWM. Conclusion: The incidence of trisomy 18 associated with DWM is rare, and our report presents an unusual case that supplements our knowledge of this condition. We report a case involving a 39-year-old pregnant female with a case of trisomy 18 associated with Dandy Walker malformation (DWM). Fetal ultrasonography showed hypoplasia of the cerebellar vermis and dilatation of the fourth ventricle and was characterized by an enlarged posterior fossa. Fetal magnetic resonance imaging showed inferior vermian hypoplasia and a large posterior fossa cyst communicating with the fourth ventricle causing high insertion of the torcular herophili, which was compatible with DWM. Furthermore, the karyotyping report revealed trisomy 18. The incidence of trisomy 18 associated with DWM is rare, and our report presents an unusual case that supplements our knowledge of this condition. (C) 2017 Taiwan Association of Obstetrics & Gynecology. Publishing services by Elsevier B.V.
引用
收藏
页码:697 / 699
页数:3
相关论文
共 15 条
  • [1] Bacino CA, 2016, NELSON TXB PEDIAT, P2802
  • [2] Prenatal diagnosis of low-level mosaicism for trisomy 18 associated with a favorable fetal outcome
    Chen, Chih-Ping
    Hung, Fang-Yu
    Chern, Schu-Rern
    Wu, Peih-Shan
    Chen, Yen-Ni
    Chen, Shin-Wen
    Lee, Meng-Shan
    Yang, Chien-Wen
    Wang, Wayseen
    [J]. TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2016, 55 (06): : 902 - 903
  • [3] First-trimester diagnosis of recurrent omphalocele associated with fetal trisomy 18 but without parental mosaicism
    Chen, Chih-Ping
    Wang, Liang-Kai
    Chern, Schu-Rern
    Kuo, Yu-Ling
    Chen, Yen-Ni
    Pan, Chen-Wen
    Wang, Wayseen
    [J]. TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2015, 54 (02): : 194 - 195
  • [4] Rapid aneuploidy diagnosis of trisomy 18 by array comparative genomic hybridization using uncultured amniocytes in a pregnancy with fetal arachnoid cyst detected in late second trimester
    Chen, Chih-Ping
    Su, Yi-Ning
    Weng, Shun-Long
    Tsai, Fuu-Jen
    Chen, Chen-Yu
    Liu, Yu-Peng
    Chern, Schu-Rern
    Chen, Wen-Lin
    Wu, Pei-Chen
    Wang, Wayseen
    [J]. TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2012, 51 (03): : 481 - 484
  • [5] Chervenak FA, 2003, OBSTET GYNECOL SURV, V58, P473
  • [6] DANDY-WALKER VARIANT - PRENATAL SONOGRAPHIC FEATURES AND CLINICAL OUTCOME
    ESTROFF, JA
    SCOTT, MR
    BENACERRAF, BR
    [J]. RADIOLOGY, 1992, 185 (03) : 755 - 758
  • [7] Feticide Peckham C., 2010, TERMINATION PREGNANC, P29
  • [8] Imataka George, 2007, Congenital Anomalies, V47, P113, DOI 10.1111/j.1741-4520.2007.00158.x
  • [9] Ocular Findings in a Case of Trisomy 18 With Variant of Dandy-Walker Syndrome
    Lim, Fong-Fong
    Ng, Yan-Yan
    Hu, Jui-Ming
    Chen, Suh-Jen
    Su, Pen-Hua
    Chen, Jia-Yuh
    [J]. PEDIATRICS AND NEONATOLOGY, 2010, 51 (05) : 292 - 295
  • [10] Millen KJ, 2012, SWAIMANS PEDIAT NEUR, P160