Cytogenomic Abnormalities in 19 Cases of Salivary Gland Tumors of Parotid Gland Origin. (2nd December 2020)

• Record Type: Journal Article
• Authors: Zerjav, Marie; DiAdamo, Autumn; Grommisch, Brittany; Katherine, Amato; Chai, Hongyan; Peng, Gang; Li, Peining
• Other Names: Paracchini Silvia Academic Editor.
• Is Part Of: Case reports in genetics. Volume 2020(2020)
• Publication Date: 2020-12-02
• Subjects: Genetics -- Periodicals; Genetics -- Case studies -- Periodicals; Genetics; Genetic Phenomena; Genetics; Periodicals; Case studies; Periodicals; Case Reports; Fulltext; Internet Resources; Periodicals; 576.5
• DOI: 10.1155/2020/8897541
• Languages: English
• ISSNs: 2090-6544

Abstract

Abstract : Salivary gland tumors (SGTs) of parotid origin are a group of diverse neoplasms which are difficult to classify due to their rarity and similar morphologic patterns. Chromosome analysis can detect clonal abnormalities, and array comparative genomic hybridization (aCGH) analysis can define copy number alterations (CNAs) from tumor specimens. Of the 19 cases of various types of SGTs submitted for cytogenomic analyses, an abnormal clone was detected in nine cases (47%), and CNAs were detected in 14 cases (74%). Recurrent rearrangements involving the PLAG1 gene at 8q12, recurrent CNAs including deletions of 6q, 9p (CDKN2A), and 17p (TP53), loss of Y chromosome, and gain of chromosome 7 were defined from these cases. Combined karyotyping and aCGH analyses could improve diagnostic yield. Future study for more precisive correlation of SGT classification with cytogenomic abnormalities will facilitate better diagnosis and treatment.