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巨大垂体大腺瘤伴卒中表现为孤立性双侧舌下神经麻痹:病例说明

Giant pituitary macroadenoma with apoplexy presenting with isolated bilateral hypoglossal nerve palsy: illustrative case.

作者信息

Zaher Mazen, Kolmetzky Devin W, Al-Atrache Zein, Vimawala Swar, Kolia Nadeem R, Godil Saniya S

机构信息

Departments of Neurosurgery, Cooper University, Camden, New Jersey.

Departments of Otolaryngology-Head and Neck Surgery, Cooper University, Camden, New Jersey.

出版信息

J Neurosurg Case Lessons. 2024 Sep 30;8(14). doi: 10.3171/CASE24326.

DOI:10.3171/CASE24326
PMID:39348723
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11445864/
Abstract

BACKGROUND

Giant pituitary prolactinomas are rare entities that can present with pituitary apoplexy and acute neurological decline. Isolated acute hypoglossal nerve palsy is an extremely rare presentation that is not well described in the literature. The authors describe the case of a giant prolactin-secreting adenoma with apoplexy that presented with isolated bilateral hypoglossal palsy, followed by a brief review of the literature and management strategies.

OBSERVATIONS

A 62-year-old female with a history of neck pain presented after a syncopal episode with dysarthria and dysphagia attributed to bilateral hypoglossal nerve palsies. Magnetic resonance imaging revealed a giant apoplectic pituitary tumor with extensive suprasellar and clival extension, including clear invasion of bilateral occipital condyles on computed tomography. The patient underwent urgent endoscopic transsphenoidal decompression and debulking of her tumor and was started on medical therapy with immediate, significant improvement in the bilateral hypoglossal nerve palsies.

LESSONS

Prolactinomas presenting with acute neurological decline, including bilateral hypoglossal nerve palsy, can benefit from urgent endoscopic transsphenoidal surgical decompression and safe debulking. Bilateral condylar tumor invasion may not always require craniocervical surgical fixation in the acute setting. Patients should be followed up and monitored clinically and radiographically for any signs of craniocervical instability after the initiation of medical therapy. https://thejns.org/doi/10.3171/CASE24326.

摘要

背景

巨大垂体泌乳素瘤是一种罕见的疾病,可表现为垂体卒中及急性神经功能障碍。孤立性急性舌下神经麻痹是一种极其罕见的表现,文献中对此描述不多。作者报告了一例巨大分泌泌乳素腺瘤伴卒中,表现为孤立性双侧舌下神经麻痹的病例,并对相关文献及治疗策略进行了简要回顾。

观察结果

一名62岁有颈部疼痛病史的女性,在晕厥发作后出现构音障碍和吞咽困难,原因是双侧舌下神经麻痹。磁共振成像显示一个巨大的卒中垂体瘤,向鞍上及斜坡广泛延伸,计算机断层扫描显示双侧枕髁有明确侵犯。患者接受了紧急内镜经蝶窦减压及肿瘤切除术,并开始接受药物治疗,双侧舌下神经麻痹立即有显著改善。

经验教训

表现为急性神经功能障碍,包括双侧舌下神经麻痹的泌乳素瘤,可从紧急内镜经蝶窦手术减压及安全的肿瘤切除术中获益。在急性情况下,双侧髁突肿瘤侵犯不一定总是需要颅颈手术固定。开始药物治疗后,应对患者进行临床及影像学随访,监测是否有颅颈不稳定的任何迹象。https://thejns.org/doi/10.3171/CASE24326

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Management of giant prolactinoma causing craniocervical instability: illustrative case.导致颅颈不稳定的巨大泌乳素瘤的治疗:病例说明
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