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小唾液腺涎腺乳头瘤的临床病理研究:8 例 BRAF V600E 突变特异性免疫组化分析的新病例系列。

Clinicopathologic Study of Sialadenoma Papilliferum of the Minor Salivary Glands: A Series of 8 New Cases With BRAF V600E Mutation-specific Immunohistochemical Analysis.

机构信息

Department of Diagnostic Sciences, College of Dentistry, The University of Tennessee Health Science Center, Memphis, TN, USA.

Department of Otolaryngology - Head & Neck Surgery, College of Medicine, The University of Tennessee Health Science Center, Memphis, TN, USA.

出版信息

Int J Surg Pathol. 2023 Oct;31(7):1265-1272. doi: 10.1177/10668969221147170. Epub 2023 Jan 11.

DOI:10.1177/10668969221147170
PMID:36632022
Abstract

Sialadenoma papilliferum (SP) is a rare benign neoplasm that usually arises in the minor salivary glands. Recently, it was demonstrated that SP shares similar molecular genetic alterations ( or mutations) with its morphologic analog, syringocystadenoma papilliferum. We sought to perform clinicopathologic and immunophenotypic (BRAF V600E and SOX10) analyses on 8 new cases of SP. The cases were from 4 males and 4 females, with ages ranging from 28 to 81 years (average: 64 years). The common locations were the hard palate (n = 3) and buccal mucosa (n = 3). Histopathologically, 7 cases were classic and 1 case was oncocytic. BRAF V600E immunohistochemistry (IHC) was positive in all classic SP, involving both the exophytic and endophytic components, but negative in the oncocytic SP. SOX10 was positive in the endophytic ductal cells of the evaluated classic SP but was negative in the oncocytic SP. We report 8 new cases of this rare salivary gland neoplasm, using BRAF V600E and SOX10 IHC to further support the following points: (1) the functional role of mutation, RAS/mitogen-activated protein kinase signaling pathway in the pathogenesis of classic SP of salivary glands by IHC; (2) the analogous relationship between SP, syringocystadenoma papilliferum, and papillary seromucinous adenocarcinoma with sinonasal papilloma-like surface component (PSASP-like surface); (3) endophytic ductal component in classic SP arises from the intercalated ducts and not the excretory ducts; and (4) oncocytic SP is distinct from classic SP.

摘要

涎腺乳头状腺瘤 (SP) 是一种罕见的良性肿瘤,通常发生在小涎腺。最近,研究表明 SP 与形态学类似物,即伴大汗腺化生的涎腺乳头状囊腺瘤,具有相似的分子遗传学改变(或突变)。我们旨在对 8 例新的 SP 病例进行临床病理和免疫表型(BRAF V600E 和 SOX10)分析。这些病例来自 4 名男性和 4 名女性,年龄从 28 岁到 81 岁不等(平均:64 岁)。常见部位为硬腭(n = 3)和颊黏膜(n = 3)。组织病理学上,7 例为经典型,1 例为嗜酸细胞型。BRAF V600E 免疫组化(IHC)在所有经典型 SP 的外生性和内生性成分中均为阳性,但在嗜酸细胞型 SP 中为阴性。SOX10 在评估的经典型 SP 的内生性导管细胞中为阳性,但在嗜酸细胞型 SP 中为阴性。我们报告了 8 例这种罕见的涎腺肿瘤新病例,使用 BRAF V600E 和 SOX10 IHC 进一步支持以下观点:(1)通过 IHC 显示突变、RAS/丝裂原活化蛋白激酶信号通路在经典型 SP 发病机制中的功能作用;(2)SP、伴大汗腺化生的涎腺乳头状囊腺瘤和具有鼻内型乳头状瘤样表面成分(PSASP 样表面)的乳头状浆液黏液性腺癌之间的类似关系;(3)经典型 SP 的内生性导管成分来源于闰管,而不是排泄管;(4)嗜酸细胞型 SP 与经典型 SP 不同。

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