Teratoma-associated and so-called pure Wilms tumour of the ovary represent two separate tumour types with distinct molecular features Journal Article


Authors: Kommoss, F. K. F.; Chong, A. S.; Apellaniz-Ruiz, M.; Turashvili, G.; Park, K. J.; Hanley, K.; Valera, E. T.; von Deimling, A.; Vujanic, G.; McCluggage, W. G.; Foulkes, W. D.
Article Title: Teratoma-associated and so-called pure Wilms tumour of the ovary represent two separate tumour types with distinct molecular features
Abstract: Aims: Ovarian Wilms tumour (WT)/nephroblastoma is an extremely rare neoplasm that has been reported to occur in pure form or as a component of a teratomatous neoplasm. We hypothesized that teratoma-associated and pure ovarian WT may represent different tumour types with diverging molecular backgrounds. To test this hypothesis, we comprehensively characterized a series of five tumours originally diagnosed as ovarian WT. Methods and Results: The five cases comprised three teratoma-associated (two mature and one immature) and two pure WTs. Two of the teratoma-associated WTs consisted of small nodular arrangements of “glandular”/epithelial structures, while the third consisted of both an epithelial and a diffuse spindle cell/blastemal component. The pure WTs consisted of “glandular” structures, which were positive for sex cord markers (including inhibin and SF1) together with a rhabdomyosarcomatous component. The two pure WTs harboured DICER1 pathogenic variants (PVs), while the three associated with teratomas were DICER1 wildtype. Panel-based DNA sequencing of four of the cases did not identify PVs in the other genes investigated. Analysis of the HA19/IGF2 imprinting region showed retention of imprinting in the pure WTs but loss of heterozygosity with hypomethylation of the ICR1 region in two of three teratoma-associated WTs. Furthermore, copy number variation and clustering-based whole-genome DNA methylation analyses identified divergent molecular profiles for pure and teratoma-associated WTs. Conclusion: Based on the morphological features, immunophenotype, and molecular findings (DICER1 PVs, copy number, and DNA methylation profiles), we suggest that the two cases diagnosed as pure primary ovarian WT represent moderately to poorly differentiated Sertoli Leydig cell tumours (SLCTs), while the tumours arising in teratomas represent true WTs. It is possible that at least some prior cases reported as pure primary ovarian WT represent SLCTs. © 2023 The Authors. Histopathology published by John Wiley & Sons Ltd.
Keywords: adult; clinical article; human tissue; unclassified drug; genetics; histopathology; case report; ovarian neoplasms; gene; protein; genetic variability; pathology; wild type; dna methylation; kidney neoplasms; dead box protein; ovary; dead-box rna helicases; kidney tumor; ovary tumor; spindle cell; immunophenotyping; teratoma; heterozygosity loss; wt1 protein; rhabdomyosarcoma; estrogen receptor; progesterone receptor; tumor classification; morphological trait; ribonuclease iii; nephroblastoma; dna copy number variations; sex cord tumor; sex cord-gonadal stromal tumors; common acute lymphoblastic leukemia antigen; inhibin; mucinous cystadenoma; copy number variation; wilms tumor; transcription factor pax8; dicer1 protein, human; androblastoma; dna sequencing; humans; human; male; female; article; dicer1; dicer1 gene; blastema; sertoli-leydig cell tumour; wilms tumour; ha19 protein; igf2 protein; sf1 protein; ovary wilms tumor
Journal Title: Histopathology
Volume: 84
Issue: 4
ISSN: 0309-0167
Publisher: Wiley Blackwell  
Date Published: 2024-03-01
Start Page: 683
End Page: 696
Language: English
DOI: 10.1111/his.15116
PUBMED: 38084641
PROVIDER: scopus
PMCID: PMC11826964
DOI/URL:
Notes: Source: Scopus
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  1. Kay Jung Park
    308 Park