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黏液腺泡癌:黏液表皮样癌的一种罕见变异型。

Mucoacinar Carcinoma: A Rare Variant of Mucoepidermoid Carcinoma.

作者信息

Bundele Manish, Weinreb Ilan, Xu Bin, Chiosea Simion, Faquin William, Dias-Santagata Dora, Leon Marino, Hyrcza Martin, Seethala Raja R

机构信息

Tang Tock Seng Hospital, Tang Tock Seng, Singapore.

Department of Laboratory Medicine & Pathobiology, University Health Network, Toronto, ON.

出版信息

Am J Surg Pathol. 2021 Aug 1;45(8):1028-1037. doi: 10.1097/PAS.0000000000001752.

Abstract

Mucoepidermoid carcinoma (MEC) is generally characterized by an admixture of mucous, epidermoid and intermediate type cells. Numerous variants morphologies are described and defined by stromal and/or cytoplasmic tinctorial characteristics. We now report 11 cases of MEC with serous acinar differentiation, reflecting a distal intercalated duct/acinar phenotype, which we designate as mucoacinar carcinomas. Seven patients were female while 4 were male with a mean age of 55 years (range: 21 to 72 y). Ten cases were from the parotid while 1 was from the submandibular gland. Mean size of the tumors was 1.8 cm (range: 0.7 to 4.5 cm). Three cases were low grade, 7 were intermediate grade, and 1 was high grade. Low to intermediate grade cases demonstrated prominent clear to vacuolated cells with focal serous acinar differentiation. The high-grade case showed a distinctive scattering of acinar cells interspersed between epidermoid cells. Periodic acid Schiff after diastase (9/9), SOX-10 (9/9), and DOG-1 (9/10) highlighted the acinar component. Six of 7 cases showed a focal acinar predominant NR4A3 expression. MAML2 fluorescence in situ hybridization was positive in all cases, in both acinar and mucoepidermoid components. Two cases tested by next generation sequencing showed standard CRTC1-MAML2 fusions. MSANTD3 and NR4A3 fluorescence in situ hybridization on the other hand were negative. Evidence thus suggests that mucoacinar carcinoma represents an acinar variant morphology in MEC, rather than a true MEC-acinic cell carcinoma hybrid, or collision tumor. The acinar differentiation, SOX-10, DOG-1, and even focal NR4A3 reactivity may thus be diagnostic pitfalls.

摘要

黏液表皮样癌(MEC)通常以黏液、表皮样和中间型细胞混合为特征。通过基质和/或细胞质染色特征描述并定义了许多变异形态。我们现报告11例具有浆液性腺泡分化的MEC病例,反映出远端闰管/腺泡表型,我们将其命名为黏液腺泡癌。7例患者为女性,4例为男性,平均年龄55岁(范围:21至72岁)。10例来自腮腺,1例来自下颌下腺。肿瘤平均大小为1.8 cm(范围:0.7至4.5 cm)。3例为低级别,7例为中级别,1例为高级别。低级别至中级别病例表现为显著的透明至空泡状细胞,并伴有局灶性浆液性腺泡分化。高级别病例显示腺泡细胞散在分布于表皮样细胞之间。淀粉酶消化后的过碘酸希夫染色(9/9)、SOX-10(9/9)和DOG-1(9/10)突出了腺泡成分。7例中的6例显示局灶性腺泡为主的NR4A3表达。所有病例的MAML2荧光原位杂交均为阳性,腺泡和黏液表皮样成分均如此。2例经下一代测序检测显示标准的CRTC1-MAML2融合。另一方面,MSANTD3和NR4A3荧光原位杂交为阴性。因此,有证据表明黏液腺泡癌代表MEC中的一种腺泡变异形态,而非真正的MEC-腺泡细胞癌混合型或碰撞瘤。因此,腺泡分化、SOX-10、DOG-1甚至局灶性NR4A3反应性可能是诊断陷阱。

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