ArticleVirchows Archiv : an international journal of pathology2025
Conundrum of 3N: nasopharyngeal nonkeratinizing non-viral carcinoma-reappraisal of fusions and report of two consecutive cases with unusual molecular findings.
Article in Virchows Archiv : an international journal of pathology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 3 papers.
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Who cites it
3 citing papers in PubMed.
- Skin-analogue primary poroid neoplasms of the head and neck with YAP1/WWTR1::MAML2/NUTM1 fusions: clinicopathologic and genetic spectrum of a novel tumor family delineated in a series of 10 cases.Virchows Archiv : an international journal of pathology · 2026Article
- Recent developments in salivary gland pathology after the WHO 2024 classification: new developments in existing entities and evolving new entities.Virchows Archiv : an international journal of pathology · 2026Review
- FGFR3::TACC3 fusions in head and neck carcinomas: a study of nine cases highlighting phenotypic heterogeneity, frequent HPV association, and a morphologically distinct subset in favor of a putative entity.Virchows Archiv : an international journal of pathology · 2025Article
Corrections and comments
- Erratum issued
Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Nasopharyngeal carcinoma (NPC) has a unique and complex etiology that is not completely understood. NPC genome has been scrutinized by molecular studies, but small biopsy material and heavy infiltration of nonmalignant cells present major technical challenges. Over the past decade, significant progress in sinonasal tumor taxonomy has taken place with the discovery of tumor-specific fusion oncogenes generated by chromosomal translocation information. We report two consecutive nonviral-associated nonkeratinizing NPCs and their integrated morphological, phenotypical, and molecular characterization, with emphasis on fusions. Both NPCs harbored individual fusions, YAP1::MAML2 and FGFR3::TACC3,respectively.
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