鞍原发乳头状上皮肿瘤1例,极性相反,盒8成对表达。

IF 3 3区 医学 Q2 CLINICAL NEUROLOGY
MingXun Zhang, AnLi Zhang, Yuan Li, Wei Wang, HaiBo Wu
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引用次数: 0

摘要

原发性蝶鞍乳头状上皮瘤(PPETS)是一种罕见的蝶鞍肿瘤,其特征是独特的乳头状结构和甲状腺转录因子1 (TTF-1)的表达。DNA甲基化分析提示其属于垂体后叶肿瘤类别。在此,我们报告一例以闭经为表现的37岁女性PPETS,具有独特的形态学和免疫组织化学特征。肿瘤表现出非典型的逆转核极性,值得注意的是,显示出配对框8 (PAX-8)和突触素的阳性表达,这些结果在pet中未见报道。经过综合评估,包括DNA甲基化分析和排除转移性疾病,肿瘤被归类为垂体后叶肿瘤,证实了pet的诊断。本病例扩展了已知的pet形态学和免疫组织化学谱,强调了垂体腺瘤和转移性癌仔细鉴别诊断的重要性。进一步的研究是必要的,以充分表征形态变异和免疫表型多样性的这种罕见的肿瘤类型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A case of primary papillary epithelial tumor of the sella with reverse polarity and paired box 8 expression.

Primary papillary epithelial tumor of the sella (PPETS) is a rare sellar neoplasm characterized by distinctive papillary architecture and thyroid transcription factor 1 (TTF-1) expression. DNA methylation profiling suggests its classification within the posterior pituitary tumor category. Here, we report a case of PPETS in a 37 year-old female presenting with amenorrhea, featuring unique morphological and immunohistochemical characteristics. The tumor exhibited atypical reversed nuclear polarity and, notably, demonstrated positive expression of paired box 8 (PAX-8) and synaptophysin-findings not previously reported in PPETS. Following comprehensive evaluation, including DNA methylation analysis and exclusion of metastatic disease, the tumor was classified as a posterior pituitary tumor, confirming the diagnosis of PPETS. This case expands the known morphological and immunohistochemical spectrum of PPETS, highlighting the importance of careful differential diagnosis from pituitary adenomas and metastatic carcinomas. Further investigation is warranted to fully characterize the morphological variants and immunophenotypic diversity of this rare tumor type.

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来源期刊
Brain Tumor Pathology
Brain Tumor Pathology 医学-病理学
CiteScore
5.40
自引率
9.10%
发文量
30
审稿时长
>12 weeks
期刊介绍: Brain Tumor Pathology is the official journal of the Japan Society of Brain Tumor Pathology. This international journal documents the latest research and topical debate in all clinical and experimental fields relating to brain tumors, especially brain tumor pathology. The journal has been published since 1983 and has been recognized worldwide as a unique journal of high quality. The journal welcomes the submission of manuscripts from any country. Membership in the society is not a prerequisite for submission. The journal publishes original articles, case reports, rapid short communications, instructional lectures, review articles, letters to the editor, and topics.Review articles and Topics may be recommended at the annual meeting of the Japan Society of Brain Tumor Pathology. All contributions should be aimed at promoting international scientific collaboration.
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