Microsecretory Adenocarcinoma A Novel Salivary Gland Tumor Characterized by a Recurrent MEF2C-SS18 Fusion

被引:77
作者
Bishop, Justin A. [1 ,2 ]
Weinreb, Ilan [4 ,5 ]
Swanson, David [5 ,6 ]
Westra, William H. [7 ]
Qureshi, Hina S. [8 ]
Sciubba, James [3 ]
MacMillan, Christina [5 ,6 ]
Rooper, Lisa M. [2 ]
Dickson, Brendan C. [5 ,6 ]
机构
[1] UT Southwestern Med Ctr, Dept Pathol, Dallas, TX USA
[2] Johns Hopkins Univ Hosp, Dept Pathol, Baltimore, MD 21287 USA
[3] Greater Baltimore Med Ctr, Milton J Dance Jr Head & Neck Ctr, Baltimore, MD USA
[4] Univ Hlth Network, Dept Pathol, Toronto, ON, Canada
[5] Univ Toronto, Dept Lab Med & Pathobiol, Toronto, ON, Canada
[6] Mt Sinai Hosp, Dept Pathol & Lab Med, Toronto, ON, Canada
[7] Mt Sinai Hosp, Dept Pathol, Icahn Sch Med, New York, NY 10029 USA
[8] ProDia Labs, Charlottesville, VA USA
关键词
salivary glands; adenocarcinoma not otherwise specified; secretory carcinoma; polymorphous adenocarcinoma; IN-SITU-HYBRIDIZATION; CLEAR-CELL CARCINOMA; MAML2; REARRANGEMENTS; GENES; IDENTIFICATION; TRANSCRIPT; MUCOSA; HEAD; SYT; BOX;
D O I
10.1097/PAS.0000000000001273
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Salivary gland adenocarcinoma not otherwise specified (NOS) is a heterogenous group, likely containing distinct tumors not yet characterized. A growing number of low to intermediate-grade salivary carcinomas are now known to harbor tumor-specific gene fusions. On occasion, identifying a novel fusion allows for recognition of a new salivary tumor type, in addition to representing a potential diagnostic tool. We sought to characterize a distinctive salivary gland adenocarcinoma that would previously have been regarded as adenocarcinoma NOS. On the basis of the recognition of 5 morphologically identical, distinct low-grade salivary adenocarcinomas, we used targeted RNA sequencing (RNA-Seq) to determine whether these could be differentiated from other fusion-associated salivary gland tumors. RNA-Seq was performed on all 5 low-intermediate grade adenocarcinomas NOS with near-identical histologic appearances, as well as 23 low-intermediate grade control adenocarcinoma NOS cases that did not resemble the index cases. All 5 index cases harbored a novel MEF2C-SS18 gene fusion, which was independently confirmed by reverse transcriptase-polymerase chain reaction. The MEF2C-SS18-positive cases arose in the oral cavity (4/5) and parotid gland (1/5) of 3 women and 2 men ranging from 21 to 80 years (mean: 46) and shared near-identical histologic features: intercalated duct-like cells with eosinophilic to clear cytoplasm and small, uniform oval nuclei, infiltrative microcysts and cords, abundant intraluminal secretions, and cellular fibromyxoid stroma. Mitotic rates were low; necrosis was absent. All MEF2C-SS18-positive tumors were positive for S100 and p63 and negative for p40, smooth muscle actin, calponin, and mammaglobin. One of the 23 control cases, a parotid tumor, was found to contain a SS18-ZBTB7A gene fusion; it demonstrated similar, but not identical histologic and immunophenotypic features compared with the MEF2C-SS18 cases. The remaining control cases were negative for SS18 and MEF2C rearrangements. A novel MEF2C-SS18 gene fusion and unique histologic and immunophenotypic features characterize a heretofore undefined low-grade salivary adenocarcinoma for which we propose the term "microsecretory adenocarcinoma." RNA-Seq helped establish this entity as a distinct tumor type, and identified one possibly related case with a different SS18-related fusion. The recognition of microsecretory adenocarcinoma and its separation from other adenocarcinomas NOS will facilitate a more complete understanding of the clinical and pathologic characteristics of this previously unrecognized neoplasm.
引用
收藏
页码:1023 / 1032
页数:10
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