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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.
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页码:1023 / 1032
页数:10
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