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Sinonasal Undifferentiated Carcinoma (SNUC): From an Entity to Morphologic Pattern and Back Again-A Historical Perspective
A. Agaimy, A. Franchi, VJ. Lund, A. Skálová, JA. Bishop, A. Triantafyllou, S. Andreasen, DR. Gnepp, H. Hellquist, LDR. Thompson, A. Rinaldo, A. Ferlito,
Language English Country United States
Document type Journal Article, Review
- MeSH
- DNA Helicases genetics MeSH
- SMARCB1 Protein genetics MeSH
- Nuclear Proteins genetics MeSH
- Carcinoma diagnosis epidemiology genetics MeSH
- Humans MeSH
- Biomarkers, Tumor genetics MeSH
- Maxillary Sinus Neoplasms diagnosis epidemiology genetics MeSH
- Transcription Factors genetics MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Review MeSH
Since the first description of sinonasal undifferentiated carcinoma (SNUC) as a distinctive highly aggressive sinonasal neoplasm with probable origin from the sinonasal mucosa (Schneiderian epithelium), SNUC has been the subject of ongoing study and controversy. In particular, the SNUC category gradually became a "wastebasket" for any undifferentiated or unclassifiable sinonasal malignancy of definite or probable epithelial origin. However, with the availability of more specific and sensitive immunohistochemical antibodies and increasing implementation of novel genetic tools, the historical SNUC category became the subject of progressive subdivision leading to recognition of specific genetically defined, reproducible subtypes. These recently recognized entities are characterized by distinctive genetic aberrations including NUTM1-rearranged carcinoma (NUT carcinoma) and carcinomas associated with inactivation of different members of the SWI/SNF chromatin-remodeling gene complex such as SMARCB1-deficient and less frequently SMARCA4-deficient carcinoma. The ring became almost closed, with recent studies highlighting frequent oncogenic IDH2 mutations in the vast majority of histologically defined SNUCs, with a frequency of 82%. A review of these cases suggests the possibility that "true SNUC" probably represents a distinctive neoplastic disease entity, morphologically, phenotypically, and genetically. This review addresses this topic from a historical perspective, with a focus on recently recognized genetically defined subsets within the SNUC spectrum.
Alpert Medical School at Brown University Providence RI
Department of Pathology Charles University Faculty of Medicine in Plzen Plzen Czech Republic
Department of Pathology Southern California Permanente Medical Group Woodland Hills CA
Department of Pathology University of Texas Southwestern Medical Center Dallas TX
Department of Translational Research School of Medicine University of Pisa Pisa
International Head and Neck Scientific Group Padua Italy
Royal National Throat Nose and Ear Hospital University College London Hospitals London
References provided by Crossref.org
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