三鞍碰撞性病变:垂体腺瘤、Rathke裂性囊肿及黄色肉芽肿个案报告及文献系统复习。

IF 2.7 3区 医学 Q2 CLINICAL NEUROLOGY
Miguel A Del Toro-Colín, Martha Tena-Suck, Alberto Santiago-Balmaseda, Citlalteptl Salinas-Lara, Germán Velázquez-Garcia, Maria de Lourdes Aguilar-Gómez, Elsa Yazmín León-Marroquín, Carlos Sánchez-Garibay, Alma Ortíz-Plata, Roger Carrillo-Meza, Noemi Gelista-Herrera, Lesly Hernández-Roque, Luis O Soto-Rojas
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引用次数: 0

摘要

鞍区同时出现三种病灶是极为罕见的。只有两个病例有三个组织病理学上不同的病变被报道。然而,在这里,我们提出一个独特的病例,54岁的女性垂体腺瘤(PA),黄色肉芽肿性垂体炎(XGH)和Rathke裂性囊肿(RCC)。临床表现为中强度头痛、进行性视力下降等团块受压症状。相关内分泌检查显示游离甲状腺素水平升高,无临床表现。MRI显示鞍上肿块与大腺瘤相吻合。患者接受了经蝶窦内镜切除,由于RCC破裂导致无功能大腺瘤伴XGH。此外,在本文中,我们分析了这些病变发病机制的可能机制,强调了它们所属的频谱类型和目前的表现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Triple sellar collision lesion: a unique case of pituitary adenoma, Rathke cleft cyst, and xanthogranuloma-case report and systematic review of the literature.

The coexistence of three lesions in the sellar region is exceedingly rare. Only two cases with three histopathologically distinct lesions have been reported. However, here, we present a unique case of a 54-year-old female with pituitary adenoma (PA), xanthogranulomatous hypophysitis (XGH), and a Rathke cleft cyst (RCC). Clinically, the patient manifested symptoms of mass compression, such as moderate-intensity headaches and progressive visual acuity decrease. Relevant endocrinological evaluation revealed elevated free thyroxine levels without clinical manifestations. MRI revealed a suprasellar mass compatible with a macroadenoma. The patient underwent transsphenoidal endoscopic resection, resulting in a non-functional macroadenoma with associated XGH due to the rupture of RCC. Furthermore, in this article, we analyze the possible mechanisms involved in the pathogenesis of these lesions, emphasizing the type of spectrum to which they belong and the manifestations present.

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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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