晚期复发伴MN1改变的星形母细胞瘤的独特病理表现。

IF 2.7 3区 医学 Q2 CLINICAL NEUROLOGY
Brain Tumor Pathology Pub Date : 2021-07-01 Epub Date: 2021-04-28 DOI:10.1007/s10014-021-00401-6
Masaki Ujihara, Kazuhiko Mishima, Atsushi Sasaki, Jun-Ichi Adach, Mitsuaki Shirahata, Tomonari Suzuki, Sumihito Nobusawa, Ryo Nishikawa
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引用次数: 3

摘要

星形母细胞瘤是一种极其罕见的脑肿瘤,由于其与MN1基因改变有关,最近引起了人们的关注。然而,其长期临床病程尚不清楚。我们报告一例晚期复发的mn1改变的星形母细胞瘤,具有独特的病理表现。一名24岁女性因左额叶肿瘤而癫痫发作。经大体全切除(GTR),诊断为mn1改变的星形母细胞瘤,表现为细胞包裹,即肿瘤细胞相互包裹。局部放疗(50 Gy)。然而,12年后肿瘤复发,体积迅速增大。第二次手术达到了GTR,并证实了间变性增加。患者无肿瘤1年,无任何神经功能缺损。本病例提示长期随访mn1改变星形母细胞瘤的重要性。本例中细胞包裹的病理意义尚不清楚,但它可能与mn1改变的星形母细胞瘤有关,在未来的病例中应予以注意。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Unique pathological findings of astroblastoma with MN1 alteration in a patient with late recurrence.

Astroblastoma is an extremely rare brain tumor that has recently attracted attention owing to its association with MN1 gene alteration. However, its long-term clinical course remains unclear. We report a late recurrence of MN1-altered astroblastoma with unique pathological findings. A 24-year-old woman presented with seizures due to a left frontal lobe tumor. Gross total resection (GTR) was achieved, and the diagnosis was MN1-altered astroblastoma, which presented cell wrapping, i.e., presence of tumor cells enveloping one another. She received local radiotherapy (50 Gy). However, the tumor recurred after 12 years, and its size increased rapidly. The second surgery achieved GTR and confirmed increasing anaplasia. The patient was tumor-free for 1 year without any neurological deficits. This case implies the importance of long-term follow-up of MN1-altered astroblastoma. The pathological significance of cell wrapping in this case is unclear, but it may be associated with MN1-altered astroblastoma and should be noted in future cases.

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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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