Temporomandibular joint (TMJ) lesions with intracranial extension: illustrative cases from a systematic review of the literature and our institution.

Hayley McKee, Taryn Rohringer, Andrew Z Yang, Yash Patel, Laila Alshafai, Emma Blanchette, Christine M Glastonbury, Pascal J Mosimann, Jürgen Germann, Shivaprakash Hiremath, Alexandre Boutet
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引用次数: 0

Abstract

Background: Intracranially extending temporomandibular joint (TMJ) lesions may be radiologically misinterpreted as primary intracranial or skull base pathologies, leading to diagnostic delays or inappropriate management.

Purpose: This systematic review aimed to characterize the clinical and imaging features of such TMJ lesions and evaluate the impact of radiologic misclassification. We also aimed to develop a diagnostic framework for when to consider an intracranially extending TMJ lesion, based on clinical and radiologic features.

Data sources: A comprehensive search of MEDLINE, SCOPUS, and Embase, conducted in accordance with PRISMA guidelines, yielded 2,255 records.

Study selection: After screening with a pre-determined inclusion and exclusion criteria, 128 studies involving 152 patients were included in the final analysis.

Data analysis: Statistical analyses were performed using STATA software. We also identified 3 patient cases through our institutional neuroradiology practice who were clinically and radiologically assessed for intracranially extending TMJ lesions.

Data synthesis: Patients had symptoms for an average of 34 months prior to diagnosis (47% female, mean age 50 years). The most common pathologies were pigmented villonodular synovitis/tenosynovial giant cell tumor (43%) and synovial chondromatosis (24%). Neurological symptoms were reported in 48% of cases, most frequently hearing loss (70%). Nearly one-third (33%) of cases with an imaging differential did not list a TMJ pathology (18/55). In cases with accurate imaging diagnosis, 90% had both CT and MRI performed. Most lesions were non-enhancing (CT 83%, MRI 75%) and demonstrated no adjacent brain edema (96%). In two cases, a TMJ ganglion cyst and pseudogout were misdiagnosed as intracranial tumors, resulting in unnecessary intervention, including repeat craniotomy and radiotherapy.

Limitations: Inherent biases of case report literature, including variability in the reporting of the imaging and clinical features, management and follow-up.

Conclusions: TMJ lesions with intracranial extension often present with non-specific symptoms and can mimic extra-axial tumors, leading to misdiagnosis on imaging. Recognition of hallmark imaging features, including lack of parenchymal invasion and distinct imaging patterns, may help improve radiologic accuracy and prevent overtreatment. We propose a diagnostic framework outlining when to suspect intracranially extending TMJ lesions based on clinical and imaging features, and how to avoid common diagnostic pitfalls.

颞下颌关节(TMJ)病变伴颅内扩展:来自文献和我们机构的系统回顾的说明性病例。
背景:颅内延伸颞下颌关节(TMJ)病变可能在影像学上被误解为原发性颅内或颅底病变,导致诊断延误或处理不当。目的:本系统综述旨在描述此类TMJ病变的临床和影像学特征,并评估放射学错误分类的影响。我们还旨在根据临床和放射学特征,制定一个诊断框架,以确定何时考虑向颅内延伸的TMJ病变。数据来源:根据PRISMA指南对MEDLINE、SCOPUS和Embase进行综合检索,得到2255条记录。研究选择:根据预先确定的纳入和排除标准进行筛选后,最终分析纳入128项研究,涉及152例患者。数据分析:采用STATA软件进行统计分析。我们还通过我们的机构神经放射学实践确定了3例患者,他们被临床和放射学评估为颅内扩展的TMJ病变。数据综合:患者在诊断前平均34个月出现症状(47%为女性,平均年龄50岁)。最常见的病理是色素绒毛结节性滑膜炎/腱鞘巨细胞瘤(43%)和滑膜软骨瘤病(24%)。48%的病例报告有神经系统症状,最常见的是听力损失(70%)。近三分之一(33%)的影像学差异病例未列出TMJ病理(18/55)。在影像学诊断准确的病例中,90%同时进行了CT和MRI检查。大多数病变无增强(CT 83%, MRI 75%),无邻近脑水肿(96%)。2例颞下颌神经节囊肿和假眼被误诊为颅内肿瘤,导致不必要的干预,包括重复开颅和放疗。局限性:病例报告文献的固有偏差,包括影像学和临床特征、管理和随访报告的可变性。结论:颞下颌关节病变伴颅内延伸常表现为非特异性症状,可模拟轴外肿瘤,易导致影像学误诊。识别标志性的影像学特征,包括缺乏实质侵犯和独特的影像学模式,可能有助于提高放射学准确性和防止过度治疗。我们提出了一个诊断框架,概述了根据临床和影像学特征何时怀疑颞下颌关节病变向颅内延伸,以及如何避免常见的诊断陷阱。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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