Cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes in mosaic trisomy 20 at amniocentesis in a pregnancy with a favorable outcome

被引:8
作者
Chen, Chih-Ping [1 ,2 ,3 ,4 ,5 ]
Lin, Yi-Hui [6 ]
Wu, Peih-Shan [7 ]
Chern, Schu-Rern [2 ]
Chen, Shin-Wen [1 ]
Wu, Fang-Tzu [1 ]
Lee, Chen-Chi [1 ]
Pan, Chen-Wen [1 ]
Chen, Yun-Yi [2 ]
Wang, Wayseen [2 ]
机构
[1] MacKay Mem Hosp, Dept Obstet & Gynecol, 92,Sect 2,Chung Shan North Rd, Taipei, Taiwan
[2] MacKay Mem Hosp, Dept Med Res, Taipei, Taiwan
[3] China Med Univ, Coll Chinese Med, Sch Chinese Med, Taichung, Taiwan
[4] Natl Yang Ming Chiao Tung Univ, Inst Clin & Community Hlth Nursing, Taipei, Taiwan
[5] Natl Yang Ming Chiao Tung Univ, Sch Med, Dept Obstet & Gynecol, Taipei, Taiwan
[6] Taipei Med Univ, Wan Fang Hosp, Dept Obstet & Gynecol, Taipei, Taiwan
[7] Gene Biodesign Co Ltd, Taipei, Taiwan
来源
TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY | 2022年 / 61卷 / 01期
关键词
Amniocentesis; Cytogenetic discrepancy; Mosaic trisomy 20; Pseudomosaicism; Uncultured amniocytes; MATERNAL UNIPARENTAL DISOMY; PRENATAL-DIAGNOSIS; CHROMOSOME-20;
D O I
10.1016/j.tjog.2021.11.023
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: We present our observation of cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes in mosaic trisomy 20 at amniocentesis in a pregnancy with a favorable outcome. Case report: A 35-year-old woman underwent amniocentesis at 16 weeks of gestation because of advanced maternal age. Amniocentesis revealed a karyotype of 47,XX,+20[10]/46,XX[15]. Among 25 colonies of cultured amniocytes, 10 colonies had a karyotype of 47,XX,+20, while the rest were normal. Simultaneous array comparative genomic hybridization (aCGH) analysis on the DNA extracted from uncultured amniocytes revealed no genomic imbalance, or arr (1-22,X) x 2. The parental karyotypes were normal. Following genetic counseling, the woman underwent repeat amniocentesis at 20 weeks of gestation. Repeat amniocentesis revealed a karyotype of 47,XX,+20[3]/46,XX[35]. Among 38 colonies of cultured amniocytes, three colonies had a karyotype of 47,XX,+20, while the rest were normal. Simultaneous aCGH analysis on the DNA extracted from uncultured amniocytes revealed no genomic imbalance, or arr (1-22,X) x 2. Interphase fluorescence in situ hybridization analysis on 101 uncultured amniocytes detected only one cell with three chromosome 20 signals with a mosaic trisomy 20 level of 1% (1/101 cells), compared with 0% in normal control. Polymorphic DNA marker analysis on the DNA extracted from uncultured amniocytes and parental bloods excluded uniparental disomy 20. At 38 weeks of gestation, a phenotypically normal 3120-g female baby was delivered. Cytogenetic analysis of cord blood, placental tissue and umbilical cord revealed a karyotype of 46,XX. The neonate was normal at postnatal follow-ups. Postnatal interphase fluorescence in situ hybridization analysis on 100 buccal mucosal cells revealed no trisomy 20 signals. Conclusion: Mosaic trisomy 20 at amniocentesis can be a cultured artifact. Complete cytogenetic discrepancy may occur between cultured amniocytes and uncultured amniocytes in mosaic trisomy 20 at amniocentesis, and molecular cytogenetic analysis on uncultured amniocytes is useful for rapid distinguishing true mosaicism from pseudomosaicism under such as circumstance. (C) 2022 Taiwan Association of Obstetrics & Gynecology. Publishing services by Elsevier B.V.
引用
收藏
页码:138 / 140
页数:3
相关论文
共 16 条
[1]   Prenatal diagnosis of low-level mosaic trisomy 20 by amniocentesis in a pregnancy with a favorable outcome [J].
Chen, Chih-Ping ;
Kuo, Yu-Ling ;
Chern, Schu-Rern ;
Wu, Peih-Shan ;
Chen, Shin-Wen ;
Wu, Fang-Tzu ;
Chen, Li-Feng ;
Wang, Wayseen .
TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2020, 59 (02) :327-330
[2]   Cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes in mosaic double trisomy involving trisomy 7 and trisomy 20 (48,XY,+7,+20) at amniocentesis [J].
Chen, Chih-Ping ;
Lin, Yi-Hui ;
Chern, Schu-Rern ;
Wu, Peih-Shan ;
Chen, Shin-Wen ;
Wu, Fang-Tzu ;
Lee, Meng-Shan ;
Chen, Yun-Yi ;
Wang, Wayseen .
TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2020, 59 (01) :146-149
[3]   Discrepancy in the trisomy mosaicism level between cultured amniocytes and uncultured amniocytes in prenatally detected mosaic trisomy 20 [J].
Chen, Chih-Ping ;
Chang, Shuenn-Dyh ;
Chueh, Ho-Yen ;
Su, Yi-Ning ;
Chern, Schu-Rern ;
Su, Jun-Wei ;
Chen, Yu-Ting ;
Chen, Wen-Lin ;
Lee, Meng-Shan ;
Wang, Wayseen .
TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2013, 52 (01) :145-146
[4]   High frequency of paternal iso or heterodisomy at chromosome 20 associated with sporadic pseudohypoparathyroidism 1B [J].
Colson, Cindy ;
Decamp, Matthieu ;
Gruchy, Nicolas ;
Coudray, Nadia ;
Ballandonne, Celine ;
Bracquemart, Claire ;
Molin, Arnaud ;
Mittre, Herve ;
Takatani, Rieko ;
Juppner, Harald ;
Kottler, Marie-Laure ;
Richard, Nicolas .
BONE, 2019, 123 :145-152
[5]   Identification of interstitial maternal uniparental disomy (UPD) (14) and complete maternal UPD(20) in a cohort of growth retarded patients [J].
Eggermann, T ;
Mergenthaler, S ;
Eggermann, K ;
Albers, A ;
Linnemann, K ;
Fusch, C ;
Ranke, MB ;
Wollmann, HA .
JOURNAL OF MEDICAL GENETICS, 2001, 38 (02) :86-89
[6]   upd(20)mat is a rare cause of the Silver-Russell-syndrome-like phenotype: Two unrelated cases and screening of large cohorts [J].
Hjortshoj, Tina D. ;
Sorensen, Anna R. ;
Yusibova, Melodi ;
Hansen, Bo M. ;
Duno, Morten ;
Balslev-Harder, Marie ;
Gronskov, Karen ;
van Hagen, Johanna M. ;
Polstra, Abeltje M. ;
Eggermann, Thomas ;
Finken, Martijn J. J. ;
Tuemer, Zeynep .
CLINICAL GENETICS, 2020, 97 (06) :902-907
[7]   TRISOMY-20 MOSAICISM IN PRENATAL-DIAGNOSIS - A REVIEW AND UPDATE [J].
HSU, LYF ;
KAFFE, S ;
PERLIS, TE .
PRENATAL DIAGNOSIS, 1987, 7 (08) :581-596
[8]   Prenatal diagnosis of mosaic trisomy 20 in New Zealand [J].
James, PA ;
Gibson, K ;
McGaughran, J .
AUSTRALIAN & NEW ZEALAND JOURNAL OF OBSTETRICS & GYNAECOLOGY, 2002, 42 (05) :486-489
[9]   Maternal Uniparental Disomy for Chromosome 20: Physical and Endocrinological Characteristics of Five Patients [J].
Kawashima, Sayaka ;
Nakamura, Akie ;
Inoue, Takanobu ;
Matsubara, Keiko ;
Horikawa, Reiko ;
Wakui, Keiko ;
Takano, Kyoko ;
Fukushima, Yoshimitsu ;
Tatematsu, Toshi ;
Mizuno, Seiji ;
Tsubaki, Junko ;
Kure, Shigeo ;
Matsubara, Yoichi ;
Ogata, Tsutomu ;
Fukami, Maki ;
Kagami, Masayo .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2018, 103 (06) :2083-2088
[10]   Maternal uniparental disomy of chromosome 20: a novel imprinting disorder of growth failure [J].
Mulchandani, Surabhi ;
Bhoj, Elizabeth J. ;
Luo, Minjie ;
Powell-Hamilton, Nina ;
Jenny, Kim ;
Gripp, Karen W. ;
Elbracht, Miriam ;
Eggermann, Thomas ;
Turner, Claire L. S. ;
Temple, I. Karen ;
Mackay, Deborah J. G. ;
Dubbs, Holly ;
Stevenson, David A. ;
Slattery, Leah ;
Zackai, Elaine H. ;
Spinner, Nancy B. ;
Krantz, Ian D. ;
Conlin, Laura K. .
GENETICS IN MEDICINE, 2016, 18 (04) :309-315