纹状导管腺瘤:病例报告与范围综述

IF 3.2 Q2 PATHOLOGY
Roberta Rayra Martins-Chaves, Maria Clara Martins Avelar, Artur Luiz Dias Ferreira, Angellica Pereira de Almeida, Gabriel Vasconcellos Sabido Gomes, Pedro Lobo Alcântra Neves, Felipe Paiva Fonseca, Ricardo Santiago Gomez
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引用次数: 0

摘要

简介条状导管腺瘤(SDA)是一种罕见的良性唾液腺肿瘤,具有最近描述的遗传特征。影响 IDH2 基因的复发性致癌突变将 SDA 从其主要的鉴别诊断管状腺瘤中区分出来。在此,我们报告了一例影响腮腺的 SDA,其 IDH1/2 基因突变特异性免疫组化阳性。此外,我们还根据科克伦方法学(Cochrane Methodology)进行了范围界定综述,并按照乔安娜-布里格斯研究所(Joana Briggs Institute,JBI)的检查表进行了报告,以综合所有以前发表的 SDA 病例。综述协议已在开放科学框架(OSF)平台上注册 ( https://osf.io/7mztg )。检索使用 Medline、Embase、Web of Science 和 LILACS,没有日期或语言限制。对研究进行了资格评估、提取,并以叙述形式进行了汇编。对包括我们在内的七项研究进行了分析,共涉及 20 名 SDA 患者。这些肿瘤主要累及腮腺(13/20),患者平均年龄为 62 岁,没有性别倾向。肿胀是主要的临床症状。平均随访时间为 26 个月,切除后无复发或转移:对临床病理特征的认识和 IDH1/2 突变特异性免疫组化的使用是一致识别 SDA 的关键,而评估其真正的生物学潜力则需要更多的随访和检查。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Striated Duct Adenoma: A Case Report and a Scoping Review.

Introduction: Striated duct adenoma (SDA) is a rare benign salivary gland tumor with a recently described genetic signature. Recurrent oncogenic mutations affecting the IDH2 gene differentiate SDA from its primary differential diagnosis of canalicular adenoma. Here, we report a case of SDA affecting the parotid gland with IDH1/2 mutation-specific immunohistochemical positivity. Additionally, we provide a scoping review developed according to the Cochrane Methodology and reported following the Joana Briggs Institute (JBI) checklist to synthesize all previously published cases of SDA. The review protocol was registered on the Open Science Framework (OSF) platform ( https://osf.io/7mztg ). The searches were performed using Medline, Embase, Web of Science, and LILACS, with no date or language limit. Studies were evaluated for eligibility, extracted, and compiled in a narrative form. Seven studies with 20 patients with SDA, including ours, were analyzed. The tumors mainly affected the parotid gland (13/20) in patients with a mean age of 62 years and did not display sex predilection. Swelling was the leading clinical symptom. The mean follow-up duration was 26 months with no recurrence or metastasis after resection.

Conclusion: Awareness of the clinicopathological features and the use of IDH1/2 mutation-specific immunohistochemistry are pivotal for the consistent identification of SDA, and assessment for true biological potential will require increased follow-up and scrutiny.

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来源期刊
CiteScore
5.70
自引率
9.50%
发文量
99
期刊介绍: Head & Neck Pathology presents scholarly papers, reviews and symposia that cover the spectrum of human surgical pathology within the anatomic zones of the oral cavity, sinonasal tract, larynx, hypopharynx, salivary gland, ear and temporal bone, and neck. The journal publishes rapid developments in new diagnostic criteria, intraoperative consultation, immunohistochemical studies, molecular techniques, genetic analyses, diagnostic aids, experimental pathology, cytology, radiographic imaging, and application of uniform terminology to allow practitioners to continue to maintain and expand their knowledge in the subspecialty of head and neck pathology. Coverage of practical application to daily clinical practice is supported with proceedings and symposia from international societies and academies devoted to this field. Single-blind peer review The journal follows a single-blind review procedure, where the reviewers are aware of the names and affiliations of the authors, but the reviewer reports provided to authors are anonymous. Single-blind peer review is the traditional model of peer review that many reviewers are comfortable with, and it facilitates a dispassionate critique of a manuscript.
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