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涎腺导管内乳头状黏液性肿瘤和涎腺乳头状囊腺瘤的组织病理学评估:关注基因改变。

Histopathological evaluation of minor salivary gland papillary-cystic tumours: focus on genetic alterations in sialadenoma papilliferum and intraductal papillary mucinous neoplasm.

机构信息

Department of Pathology and Laboratory Medicine, Nagoya University Hospital, Nagoya, Japan.

Department of Diagnostic Pathology, School of Medicine, Fujita Health University, Toyoake, Japan.

出版信息

Histopathology. 2020 Feb;76(3):411-422. doi: 10.1111/his.13990. Epub 2019 Dec 1.

Abstract

AIMS

Minor salivary gland tumours showing a predominant papillary-cystic structure are rare, and constitute a mixture of various types of neoplasm; thus, the histopathological assessment of these tumours poses a significant diagnostic challenge. We aimed to delineate the histological characteristics of these tumours and further mutational aspects with a particular focus on sialadenoma papilliferum (SP) and intraductal papillary mucinous neoplasm (IPMN).

METHODS AND RESULTS

We retrieved 28 papillary-cystic tumours of the minor salivary glands, and performed histological re-evaluation and mutation analyses of several key oncogenes. The histological classifications were as follows: SP (n = 10), SP-like intraductal papillary tumour (SP-IPT) (n = 2), IPMN (n = 9), intraductal papilloma, cystadenoma, and cystadenocarcinoma (two, three and two respectively). Whereas SP typically consisted of a combination of exophytic squamous epithelium and endophytic intraductal papillary infoldings, SP-IPT lacked the exophytic component. SP and SP-IPT frequently harboured BRAF V600E mutations (75.0%), which were identified in both squamous and ductal components. IPMN was characterised by a well-demarcated cystic lesion filled exclusively with a papillary proliferation of mucinous cells and a high rate of AKT1 E17K mutations (88.9%). Intraductal papillomas were unilocular cystic lesions with intraluminal papillary growth of bland columnar cells. In contrast, both cystadenomas and cystadenocarcinomas showed a multicystic appearance with a papillary configuration. Cystadenocarcinomas invaded the surrounding tissue and were composed of markedly atypical tumour cells.

CONCLUSION

The appropriate interpretation of histological findings and specific genetic alterations (e.g. BRAF V600E and AKT1 E17K in SP and IPMN) would be useful for the correct diagnosis of minor salivary gland papillary-cystic tumours.

摘要

目的

以乳头状-囊性结构为主的小唾液腺肿瘤较为罕见,由多种肿瘤类型混合而成;因此,这些肿瘤的组织病理学评估具有很大的诊断挑战性。我们旨在描述这些肿瘤的组织学特征,并进一步探讨突变方面的问题,特别是针对涎腺乳头状瘤(SP)和导管内乳头状黏液性肿瘤(IPMN)。

方法和结果

我们检索了 28 例小唾液腺的乳头状-囊性肿瘤,并对几个关键的癌基因进行了组织学再评估和突变分析。组织学分类如下:SP(n=10)、SP 样管内乳头状肿瘤(SP-IPT)(n=2)、IPMN(n=9)、管内乳头状瘤、囊腺瘤和囊腺癌(分别为 2、3 和 2 例)。SP 通常由外生性鳞状上皮和内生性管内乳头状内陷组成,而 SP-IPT 缺乏外生性成分。SP 和 SP-IPT 常携带 BRAF V600E 突变(75.0%),在鳞状和导管成分中均可检测到。IPMN 的特征是界限清楚的囊性病变,仅充满黏液细胞的乳头状增生,且 AKT1 E17K 突变率较高(88.9%)。管内乳头状瘤是具有腔内乳头状生长的良性柱状细胞的单房性囊性病变。相比之下,囊腺瘤和囊腺癌均表现为多房性囊性外观,伴有乳头状结构。囊腺癌侵犯周围组织,由明显异型的肿瘤细胞组成。

结论

正确解释组织学发现和特定的遗传改变(如 SP 和 IPMN 中的 BRAF V600E 和 AKT1 E17K)对于正确诊断小唾液腺乳头状-囊性肿瘤非常有用。

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