Practical guidelines of the EOTTD for pathological and genetic diagnosis of hydatidiform moles

Carla Bartosch*, Alfons Nadal, Ana C. Braga, Angela Salerno, Anne-Laure Rougemont, Anne-Sophie Van Rompuy, Brendan Fitzgerald, Caroline Joyce, Fabienne Allias, Geoffrey J. Maher, Gitta Turowski, Jean-Christophe Tille, Kinan Drak Alsibai, Koen Van de Vijver, Lesley McMahon, Lone Sunde, Michal Pyzlak, Paul Downey, Sandra Wessman, Sophie PatrierBaljeet Kaur, Rosemary Fisher

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

6 Citations (Scopus)

Abstract

Hydatidiform moles are rare and thus most pathologists and geneticists have little experience with their diagnosis. It is important to promptly and correctly identify hydatidiform moles given that they are premalignant disorders associated with a risk of persistent gestational trophoblastic disease and gestational trophoblastic neoplasia. Improvement in diagnosis can be achieved with uniformization of diagnostic criteria and establishment of algorithms. To this aim, the Pathology and Genetics Working Party of the European Organisation for Treatment of Trophoblastic Diseases has developed guidelines that describe the pathological criteria and ancillary techniques that can be used in the differential diagnosis of hydatidiform moles. These guidelines are based on the best available evidence in the literature, professional experience and consensus of the experts' group involved in its development.

Original languageEnglish
JournalVirchows Archiv
ISSN0945-6317
DOIs
Publication statusE-pub ahead of print - 19 Oct 2023

Bibliographical note

© 2024. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

A correction to the article has been published: https://doi.org/10.1007/s00428-023-03715-2

Keywords

  • Diagnosis
  • Genetics
  • Genotyping
  • Guidelines
  • Hydatidiform moles
  • Pathology

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