• This record comes from PubMed

The Role of Molecular Testing in the Differential Diagnosis of Salivary Gland Carcinomas

. 2018 Feb ; 42 (2) : e11-e27.

Language English Country United States Media print

Document type Journal Article, Review

Salivary gland neoplasms are a morphologically heterogenous group of lesions that are often diagnostically challenging. In recent years, considerable progress in salivary gland taxonomy has been reached by the discovery of tumor type-specific fusion oncogenes generated by chromosome translocations. This review describes the clinicopathologic features of a selected group of salivary gland carcinomas with a focus on their distinctive genomic characteristics. Mammary analog secretory carcinoma is a recently described entity characterized by a t(12;15)(p13;q25) translocation resulting in an ETV6-NTRK3 fusion. Hyalinizing clear cell carcinoma is a low-grade tumor with infrequent nodal and distant metastasis, recently shown to harbor an EWSR1-ATF1 gene fusion. The CRTC1-MAML2 fusion gene resulting from a t(11;19)(q21;p13) translocation, is now known to be a feature of both low-grade and high-grade mucoepidermoid carcinomas associated with improved survival. A t(6;9)(q22-23;p23-34) translocation resulting in a MYB-NFIB gene fusion has been identified in the majority of adenoid cystic carcinomas. Polymorphous (low-grade) adenocarcinoma and cribriform adenocarcinoma of (minor) salivary gland origin are related entities with partly differing clinicopathologic and genomic profiles; they are the subject of an ongoing taxonomic debate. Polymorphous (low-grade) adenocarcinomas are characterized by hot spot point E710D mutations in the PRKD1 gene, whereas cribriform adenocarcinoma of (minor) salivary glands origin are characterized by translocations involving the PRKD1-3 genes. Salivary duct carcinoma (SDC) is a high-grade adenocarcinoma with morphologic and molecular features akin to invasive ductal carcinoma of the breast, including HER2 gene amplification, mutations of TP53, PIK3CA, and HRAS and loss or mutation of PTEN. Notably, a recurrent NCOA4-RET fusion has also been found in SDC. A subset of SDC with apocrine morphology is associated with overexpression of androgen receptors. As these genetic aberrations are recurrent they serve as powerful diagnostic tools in salivary gland tumor diagnosis, and therefore also in refinement of salivary gland cancer classification. Moreover, they are promising as prognostic biomarkers and targets of therapy.

References provided by Crossref.org

Newest 20 citations...

See more in
Medvik | PubMed

Metastatic cutaneous squamous cell carcinoma accounts for nearly all squamous cell carcinomas of the parotid gland

. 2024 Jul ; 485 (1) : 3-11. [epub] 20240417

Molecular pathology in diagnosis and prognostication of head and neck tumors

. 2024 Feb ; 484 (2) : 215-231. [epub] 20240113

Salivary gland cancer: ESMO-European Reference Network on Rare Adult Solid Cancers (EURACAN) Clinical Practice Guideline for diagnosis, treatment and follow-up

. 2022 Dec ; 7 (6) : 100602. [epub] 20221102

Development of head and neck pathology in Europe

. 2022 May ; 480 (5) : 951-965. [epub] 20220114

Update from the 5th Edition of the World Health Organization Classification of Head and Neck Tumors: Salivary Glands

. 2022 Mar ; 16 (1) : 40-53. [epub] 20220321

SalvGlandDx - a comprehensive salivary gland neoplasm specific next generation sequencing panel to facilitate diagnosis and identify therapeutic targets

. 2021 May ; 23 (5) : 473-487. [epub] 20210418

Prognostic significance of 1p36 locus deletion in adenoid cystic carcinoma of the salivary glands

. 2018 Oct ; 473 (4) : 471-480. [epub] 20180404

Polymorphous adenocarcinoma of the salivary glands: reappraisal and update

. 2018 Jul ; 275 (7) : 1681-1695. [epub] 20180514

Find record

Citation metrics

Loading data ...

Archiving options

Loading data ...