ETV6::NTRK3相关乳头状腺癌:让我们听天由命。

IF 3.4 3区 医学 Q1 PATHOLOGY
Virchows Archiv Pub Date : 2024-12-01 Epub Date: 2024-01-11 DOI:10.1007/s00428-024-03735-6
Diana Bell, Ellie Maghami, Rania Bakkar, Michelle Afkhami
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引用次数: 0

摘要

耵聍腺是位于外耳道(EAC)的改良性外分泌腺,与皮脂腺一起产生耵聍。这些结构的肿瘤性转变极为罕见。我们发现两例 EAC 腺癌与 ETV6::NTRK3 融合。尽管存在基因重叠,但其形态学和免疫表型将其与分泌性癌明确区分开来。这些病例显示了具有乳头状形态的新型原发性EAC腺癌,从而扩大了ETV6::NTRK3阳性恶性肿瘤的范围,我们将其称为ETV6::NTRK3易位相关乳头状腺癌。我们还提倡在类型或分化不确定的罕见肿瘤中使用分子技术,以增加对这些罕见肿瘤的了解和可重复分类的可能性。病理学家和肿瘤学家应该认识到这一实体,从而直接检测 NTRK 融合,以便进行适当的治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

ETV6::NTRK3-associated papillary adenocarcinoma: let us play it by ear.

ETV6::NTRK3-associated papillary adenocarcinoma: let us play it by ear.

Ceruminous glands are modified apocrine glands, situated in the external auditory canal (EAC) that, together with sebaceous glands, produce cerumen. The neoplastic transformation of these structures is exceedingly rare. We encounter two cases of EAC adenocarcinoma with ETV6::NTRK3 fusion. Despite this genetic overlap, the morphology and immunophenotype delineate its clear separation from secretory carcinoma. These cases demonstrate novel primary EAC adenocarcinoma with papillary morphology, which expands the ever-increasing list of ETV6::NTRK3-positive malignancies and which we would like to term ETV6::NTRK3-translocation associated papillary adenocarcinoma. We also advocate the use of molecular techniques in rare tumors of uncertain type or differentiation, to increase understanding and possibilities of reproducible classification of these rare neoplasms. Pathologists and oncologists should recognize this entity, which leads to a direct approach for detecting NTRK fusion for appropriate treatment.

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来源期刊
Virchows Archiv
Virchows Archiv 医学-病理学
CiteScore
7.40
自引率
2.90%
发文量
204
审稿时长
4-8 weeks
期刊介绍: Manuscripts of original studies reinforcing the evidence base of modern diagnostic pathology, using immunocytochemical, molecular and ultrastructural techniques, will be welcomed. In addition, papers on critical evaluation of diagnostic criteria but also broadsheets and guidelines with a solid evidence base will be considered. Consideration will also be given to reports of work in other fields relevant to the understanding of human pathology as well as manuscripts on the application of new methods and techniques in pathology. Submission of purely experimental articles is discouraged but manuscripts on experimental work applicable to diagnostic pathology are welcomed. Biomarker studies are welcomed but need to abide by strict rules (e.g. REMARK) of adequate sample size and relevant marker choice. Single marker studies on limited patient series without validated application will as a rule not be considered. Case reports will only be considered when they provide substantial new information with an impact on understanding disease or diagnostic practice.
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