Literature DB >> 20413680

Abnormal villous morphology associated with triple trisomy of paternal origin.

Alexis Norris-Kirby1, Jill M Hagenkord, Malti P Kshirsagar, Brigitte M Ronnett, Kathleen M Murphy.   

Abstract

The vast majority of trisomies in spontaneous abortions (SAB) are single and of maternal origin, most frequently due to meiosis I errors. Triple trisomies are exceedingly rare (approximately 0.05% of spontaneous abortions), most often of maternal origin, and associated with increased maternal age. Some trisomic SAB specimens can exhibit abnormal villous morphology simulating a partial hydatidiform mole, a distinct form of hydatidiform mole characterized by diandric triploidy. A SAB specimen from a 27-year-old woman, G1P0 at 8 weeks gestational age, was reviewed in consultation to address the finding of morphological features suggestive of a partial hydatidiform mole but DNA ploidy analysis yielding a diploid result. The villi were irregularly shaped and hydropic but lacked trophoblastic hyperplasia; p57 expression was retained. Since fully developed features of a partial hydatidiform mole were lacking, additional analysis was performed. Molecular genotyping and single nucleotide polymorphism array analysis demonstrated biparental diploidy with trisomy of chromosomes 7, 13, and 20, all of paternal origin. The three trisomies may have originated from paternal meiosis II errors, or from mitotic nondisjunction. We believe this to be the first report of triple trisomy in a SAB confirmed to be of paternal origin.

Entities:  

Mesh:

Year:  2010        PMID: 20413680      PMCID: PMC2893639          DOI: 10.2353/jmoldx.2010.090184

Source DB:  PubMed          Journal:  J Mol Diagn        ISSN: 1525-1578            Impact factor:   5.568


  34 in total

1.  Triple aneuploidy in spontaneous abortions.

Authors:  K S Reddy
Journal:  Clin Genet       Date:  1999-07       Impact factor: 4.438

2.  Persistent trophoblast disease following partial molar pregnancy.

Authors:  Sabien Wielsma; Sabien Wiesma; Linda Kerkmeijer; Ruud Bekkers; Jan Pyman; Jeffrey Tan; Michael Quinn
Journal:  Aust N Z J Obstet Gynaecol       Date:  2006-04       Impact factor: 2.100

3.  Interobserver and intraobserver variability in the diagnosis of hydatidiform mole.

Authors:  Masaharu Fukunaga; Hidetaka Katabuchi; Tetsuro Nagasaka; Yoshiki Mikami; Sachiko Minamiguchi; Janice M Lage
Journal:  Am J Surg Pathol       Date:  2005-07       Impact factor: 6.394

4.  Placental mesenchymal dysplasia associated with fetal aneuploidy.

Authors:  Marta C Cohen; Emma C Roper; Neil J Sebire; Jerzy Stanek; Dilly O C Anumba
Journal:  Prenat Diagn       Date:  2005-03       Impact factor: 3.050

5.  Persistent gestational trophoblastic neoplasia after partial hydatidiform mole incidence and outcome.

Authors:  Barry W Hancock; Kauzer Nazir; Janet E Everard
Journal:  J Reprod Med       Date:  2006-10       Impact factor: 0.142

6.  A father of four consecutive trisomic pregnancies with elevated frequencies of associated aneuploid sperm.

Authors:  Lisa M Tomascik-Cheeseman; Xiu R Lowe; Brenda Eskenazi; Sharon Kidd; Joginder Nath; Dan Moore; Andrew J Wyrobek
Journal:  Am J Med Genet A       Date:  2006-09-01       Impact factor: 2.802

Review 7.  Metastatic trophoblastic disease following partial hydatidiform mole: case report and literature review.

Authors:  J Menczer; O Girtler; L Zajdel; M Glezerman
Journal:  Gynecol Oncol       Date:  1999-08       Impact factor: 5.482

Review 8.  Meiotic chromosome abnormalities in human spermatogenesis.

Authors:  Renée H Martin
Journal:  Reprod Toxicol       Date:  2006-05-22       Impact factor: 3.143

9.  Clinical characteristics of persistent gestational trophoblastic neoplasia after partial hydatidiform molar pregnancy.

Authors:  Colleen M Feltmate; Whitfield B Growdon; Adam J Wolfberg; Donald P Goldstein; David R Genest; Manuel E Chinchilla; Ellice S Lieberman; Ross S Berkowitz
Journal:  J Reprod Med       Date:  2006-11       Impact factor: 0.142

Review 10.  The origin of human aneuploidy: where we have been, where we are going.

Authors:  Terry Hassold; Heather Hall; Patricia Hunt
Journal:  Hum Mol Genet       Date:  2007-10-15       Impact factor: 6.150

View more
  7 in total

1.  Diagnostic reproducibility of hydatidiform moles: ancillary techniques (p57 immunohistochemistry and molecular genotyping) improve morphologic diagnosis.

Authors:  Russell Vang; Mamta Gupta; Lee-Shu-Fune Wu; Anna V Yemelyanova; Robert J Kurman; Kathleen M Murphy; Cheryl Descipio; Brigitte M Ronnett
Journal:  Am J Surg Pathol       Date:  2012-03       Impact factor: 6.394

2.  Diagnostic reproducibility of hydatidiform moles: ancillary techniques (p57 immunohistochemistry and molecular genotyping) improve morphologic diagnosis for both recently trained and experienced gynecologic pathologists.

Authors:  Mamta Gupta; Russell Vang; Anna V Yemelyanova; Robert J Kurman; Fanghong Rose Li; Emily C Maambo; Kathleen M Murphy; Cheryl DeScipio; Carol B Thompson; Brigitte M Ronnett
Journal:  Am J Surg Pathol       Date:  2012-12       Impact factor: 6.394

Review 3.  Genotyping diagnosis of gestational trophoblastic disease: frontiers in precision medicine.

Authors:  Natalia Buza; Pei Hui
Journal:  Mod Pathol       Date:  2021-06-04       Impact factor: 7.842

4.  The significance of trisomy 7 mosaicism in noninvasive prenatal screening.

Authors:  Yiming Qi; Jiexia Yang; Yaping Hou; Fangfang Guo; Haishan Peng; Dongmei Wang; Qianyi Du; Aihua Yin
Journal:  Hum Genomics       Date:  2019-04-11       Impact factor: 4.639

5.  Refined diagnosis of hydatidiform moles with p57 immunohistochemistry and molecular genotyping: updated analysis of a prospective series of 2217 cases.

Authors:  Deyin Xing; Emily Adams; Jialing Huang; Brigitte M Ronnett
Journal:  Mod Pathol       Date:  2020-10-06       Impact factor: 7.842

6.  Loss of p57 Expression in Conceptions Other Than Complete Hydatidiform Mole: A Case Series With Emphasis on the Etiology, Genetics, and Clinical Significance.

Authors:  Deyin Xing; Karin Miller; Katie Beierl; Brigitte M Ronnett
Journal:  Am J Surg Pathol       Date:  2022-01-01       Impact factor: 6.298

7.  Abnormal villous morphology mimicking a hydatidiform mole associated with paternal trisomy of chromosomes 3,7,8 and unipaternal disomy of chromosome 11.

Authors:  Neil J Sebire; Philippa C May; Baljeet Kaur; Michael J Seckl; Rosemary A Fisher
Journal:  Diagn Pathol       Date:  2016-02-04       Impact factor: 2.644

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.