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Head Neck Pathol ; 17(4): 1052-1057, 2023 Dec.
Article in English | MEDLINE | ID: mdl-37847488

ABSTRACT

BACKGROUND: Lymphoepithelial carcinoma of the salivary glands (LECSG) is a rare disease in the Western hemisphere that is typically associated with an EBV infection. The molecular mechanisms of LECSG tumorigenesis are poorly understood. RESULTS: Here we report a case of EBV-associated LECSG with an unusual immunophenotype. The tumor exhibited bi-morphic histological features with a mutually exclusive expression of HER2 and p16. The p16-positive domain of the tumor immunohistochemically co-expressed late membrane protein 1 (LMP-1), while the HER2 positive domain did not. Both tumor regions expressed SSTR2. METHODS: In situ hybridization confirmed the EBV origin of the tumor while extensive immunohistochemical characterization and the recently established RNA-based next generation sequencing panel ("SalvGlandDx" panel) did not reveal evidence for another salivary gland neoplasm. No HPV co-infection was detected by in situ hybridization or PCR-based screenings and no ERBB2 gene amplification was detected by fluorescence in situ hybridization. CONCLUSION: These findings suggest tumor heterogeneity and lack of genomic aberrations in EBV-associated LECSGs. The heterogenous and unusual immunohistochemical features explain the diagnostic difficulties and simultaneously extend the immunophenotype spectrum of this tumor entity.


Subject(s)
Carcinoma, Squamous Cell , Papillomavirus Infections , Salivary Gland Neoplasms , Humans , Herpesvirus 4, Human/genetics , In Situ Hybridization, Fluorescence , Carcinoma, Squamous Cell/pathology , Salivary Glands/pathology , Salivary Gland Neoplasms/pathology , Papillomavirus Infections/complications
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