Complete hydatidiform mole with retained maternal chromosomes 6 and 11
- PMID: 19542869
- DOI: 10.1097/PAS.0b013e3181a90e01
Complete hydatidiform mole with retained maternal chromosomes 6 and 11
Abstract
Distinction of hydatidiform moles from nonmolar specimens and their subclassification as complete hydatidiform mole (CHM) versus partial hydatidiform mole (PHM) are important for clinical practice and investigational studies to refine ascertainment of risk of persistent gestational trophoblastic disease which differs among these entities. Immunohistochemical analysis of p57 expression, a paternally imprinted maternally expressed gene on 11p15.5, and molecular genotyping are useful for improving diagnosis. CHMs are characterized by androgenetic diploidy, with the loss of p57 expression owing to lack of maternal DNA. Loss of p57 expression distinguishes CHMs from both PHMs (diandric triploidy) and nonmolar specimens (biparental diploidy) which retain expression. In the process of evaluating molar specimens in our laboratory with p57 immunohistochemistry and molecular genotyping, we identified a morphologically typical androgenetic diploid CHM with aberrant diffuse p57 expression. Molecular genotyping by short tandem repeat markers and genome-wide copy number analysis by single nucleotide polymorphism array established androgenetic diploidy with retained maternal copies of chromosomes 6 and 11, with aberrant p57 expression attributable to the latter. This case, only the second reported to date, illustrates the value of combined traditional pathologic and ancillary molecular techniques for refined diagnosis of molar specimens. Specimens with morphologic features suggestive of CHM yet retaining p57 expression should be subjected to molecular genotyping to establish a definitive diagnosis because misclassification as PHM underestimates the risk of persistent gestational trophoblastic disease. We recommend use of p57 immunohistochemistry and molecular genotyping to evaluate all products of conception specimens for which there is any consideration of a diagnosis of hydatidiform mole. Genome-wide analysis has the potential to assist in localizing imprinted genes critical for determining the morphologic and behavioral phenotypes of hydatidiform moles.
Similar articles
-
Diagnosis and subclassification of hydatidiform moles using p57 immunohistochemistry and molecular genotyping: validation and prospective analysis in routine and consultation practice settings with development of an algorithmic approach.Am J Surg Pathol. 2009 Jun;33(6):805-17. doi: 10.1097/PAS.0b013e318191f309. Am J Surg Pathol. 2009. PMID: 19145201
-
Hydatidiform moles: ancillary techniques to refine diagnosis.Int J Gynecol Pathol. 2011 Mar;30(2):101-16. doi: 10.1097/PGP.0b013e3181f4de77. Int J Gynecol Pathol. 2011. PMID: 21293291 Review.
-
Characterization of androgenetic/biparental mosaic/chimeric conceptions, including those with a molar component: morphology, p57 immnohistochemistry, molecular genotyping, and risk of persistent gestational trophoblastic disease.Int J Gynecol Pathol. 2013 Mar;32(2):199-214. doi: 10.1097/PGP.0b013e3182630d8c. Int J Gynecol Pathol. 2013. PMID: 23370656
-
Diandric triploid hydatidiform mole with loss of maternal chromosome 11.Am J Surg Pathol. 2011 Oct;35(10):1586-91. doi: 10.1097/PAS.0b013e31822d5cff. Am J Surg Pathol. 2011. PMID: 21881485
-
Tetraploid partial hydatidiform mole: a case report and review of the literature.Int J Gynecol Pathol. 2012 Jan;31(1):73-9. doi: 10.1097/PGP.0b013e31822555b3. Int J Gynecol Pathol. 2012. PMID: 22123726 Review.
Cited by
-
Parental contribution to trisomy in heterozygous androgenetic complete moles.Sci Rep. 2020 Oct 13;10(1):17137. doi: 10.1038/s41598-020-74375-4. Sci Rep. 2020. PMID: 33051545 Free PMC article.
-
Paternal Hemizygosity in 11p15 in Mole-like Conceptuses: Two Case Reports.Medicine (Baltimore). 2015 Nov;94(44):e1776. doi: 10.1097/MD.0000000000001776. Medicine (Baltimore). 2015. PMID: 26554776 Free PMC article.
-
Refined diagnosis of hydatidiform moles with p57 immunohistochemistry and molecular genotyping: updated analysis of a prospective series of 2217 cases.Mod Pathol. 2021 May;34(5):961-982. doi: 10.1038/s41379-020-00691-9. Epub 2020 Oct 6. Mod Pathol. 2021. PMID: 33024305
-
Abnormal villous morphology associated with triple trisomy of paternal origin.J Mol Diagn. 2010 Jul;12(4):525-9. doi: 10.2353/jmoldx.2010.090184. Epub 2010 Apr 22. J Mol Diagn. 2010. PMID: 20413680 Free PMC article.
-
Diagnostic reproducibility of hydatidiform moles: ancillary techniques (p57 immunohistochemistry and molecular genotyping) improve morphologic diagnosis.Am J Surg Pathol. 2012 Mar;36(3):443-53. doi: 10.1097/PAS.0b013e31823b13fe. Am J Surg Pathol. 2012. PMID: 22245958 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical