Hadnagy, Viktoria S; Körner, Meike; Rössle, Matthias; Dubach, Patrick; Pabst, Gunther; Kotulova, Alexandra; Weder, Stefan; Seifert, Robert; Rushing, Elisabeth J; Holzmann, David; Hüllner, Martin; Freiberger, Sandra N; Rupp, Niels J (2024). Expanding the spectrum of low-grade sinonasal adenocarcinoma with biphasic seromucinous differentiation and activating HRAS/AKT1 mutations. (In Press). Histopathology Wiley 10.1111/his.15251
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Histopathology_-_2024_-_Hadnagy_-_Expanding_the_spectrum_of_low_grade_sinonasal_adenocarcinoma_with_biphasic_seromucinous.pdf - Published Version Available under License Creative Commons: Attribution-Noncommercial-No Derivative Works (CC-BY-NC-ND). Download (18MB) | Preview |
AIMS
Low-grade non-intestinal-type sinonasal adenocarcinoma (LGSNAC) is a rare heterogeneous and poorly characterised group of tumours, distinct from intestinal- and salivary-type neoplasms. Therefore, further characterisation is needed for clearer biological understanding and classification.
METHODS AND RESULTS
Clinical, histological and molecular characterisation of four cases of biphasic, low-grade adenocarcinomas of the sinonasal tract was performed. All patients were male, aged between 48 and 78 years, who presented with polypoid masses in the nasal cavity. Microscopically, virtually all tumours were dominated by tubulo-glandular biphasic patterns, microcystic, focal (micro)papillary, oncocytic or basaloid features. Immunohistochemical staining confirmed biphasic differentiation with an outer layer of myoepithelial cells. Molecular profiling revealed HRAS (p.G13R, p.Q61R) mutations, and concomitant AKT1 (p.E17K, p.Q79R) mutations in two cases. Two cases showed potential in-situ/precursor lesions adjacent to the tumour. Follow-up periods ranged from 1 to 30 months, with one case relapsing locally after 12 and > 20 years.
CONCLUSION
This study further corroborates a distinct biphasic low-grade neoplasm of the sinonasal tract with seromucinous differentiation. Although morphological and molecular features overlap with salivary gland epithelial-myoepithelial carcinoma, several arguments favour categorising these tumours within the spectrum of LGSNAC.
Item Type: |
Journal Article (Original Article) |
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Division/Institute: |
04 Faculty of Medicine > Department of Radiology, Neuroradiology and Nuclear Medicine (DRNN) > Clinic of Nuclear Medicine 04 Faculty of Medicine > Department of Head Organs and Neurology (DKNS) > Clinic of Ear, Nose and Throat Disorders (ENT) 04 Faculty of Medicine > Service Sector > Institute of Pathology > Clinical Pathology |
UniBE Contributor: |
Kotulova, Alexandra, Weder, Stefan Andreas, Seifert, Robert |
Subjects: |
600 Technology > 610 Medicine & health |
ISSN: |
1365-2559 |
Publisher: |
Wiley |
Language: |
English |
Submitter: |
Pubmed Import |
Date Deposited: |
27 Jun 2024 12:18 |
Last Modified: |
27 Jun 2024 18:00 |
Publisher DOI: |
10.1111/his.15251 |
PubMed ID: |
38923026 |
Uncontrolled Keywords: |
adenocarcinoma mutation paranasal sinuses salivary glands |
BORIS DOI: |
10.48350/198140 |
URI: |
https://boris.unibe.ch/id/eprint/198140 |