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初发时表现为伪装成托洛萨-亨特综合征的播散性肺结核:一例报告并文献复习

Disseminated tuberculosis masquerading as Tolosa-Hunt syndrome in initial presentation: A case report with literature review.

作者信息

Sasi Sreethish, Nair Arun Prabhakaran, Kolleri Jouhar, Alzibdeh Aseel, Maslamani Muna S Rahman Al

机构信息

Infectious Diseases Division, Department of Internal Medicine, Hamad Medical Corporation, Al Rayyan Rd., PO Box: 3050, Doha, Qatar.

Department of Clinical Imaging, Hamad Medical Corporation, Doha, Qatar.

出版信息

Radiol Case Rep. 2023 Jan 21;18(3):1353-1357. doi: 10.1016/j.radcr.2023.01.024. eCollection 2023 Mar.

Abstract

Tolosa-Hunt syndrome (THS) is a painful ophthalmoplegia due to non-specific granulomatous inflammation in the cavernous sinus region. It is diagnosed by the International Classification of Headache Disorders (ICHD)-3 criteria. We report the case of a young lady who presented with a right-sided headache for 2 weeks, followed by right-sided diplopia for 4 days. Clinical examination revealed right trochlear nerve palsy. Magnetic resonance imaging (MRI) of her brain showed abnormal thickening and postcontrast enhancement of the right orbital apex and superior orbital fissure, suggesting THS. Examination of cerebrospinal fluid (CSF) ruled out intracranial infection. The initial presentation satisfied the ICHD-3 criteria. Further imaging revealed cervical, axillary, and intra-abdominal lymphadenopathy with granulomatous lesions in the spleen and right kidney. Ultrasound (US)-guided axillary lymph node biopsy was positive for . QuantiFERON TB gold plus test from serum was positive. Based on radiological and histopathological findings, a diagnosis of disseminated tuberculosis involving lymph nodes, kidneys, spleen, and lungs was made. THS is a diagnosis of exclusion. This case signifies that patients diagnosed with THS based on ICHD-3 criteria should be extensively evaluated to rule out granulomatous infections such as tuberculosis. Typical THS symptoms with granulomatous inflammation can give false reassurance to clinicians and prevent investigation for more dangerous etiologies. As painful ophthalmoplegia can arise secondary to a myriad of pathologies, diagnostic workups for all possibilities should be exhausted before arriving at a diagnosis of THS. Regardless of MRI findings, workups for tuberculosis and fungal infections should be completed.

摘要

托洛萨-亨特综合征(THS)是一种由于海绵窦区域非特异性肉芽肿性炎症引起的疼痛性眼肌麻痹。它根据《国际头痛疾病分类》(ICHD)-3标准进行诊断。我们报告了一位年轻女性的病例,她右侧头痛2周,随后右侧复视4天。临床检查发现右侧滑车神经麻痹。她脑部的磁共振成像(MRI)显示右侧眶尖和眶上裂异常增厚且增强后强化,提示为THS。脑脊液(CSF)检查排除了颅内感染。初始表现符合ICHD-3标准。进一步的影像学检查显示颈部、腋窝和腹腔内淋巴结肿大,脾脏和右肾有肉芽肿性病变。超声(US)引导下的腋窝淋巴结活检呈阳性。血清结核感染T细胞检测(QuantiFERON TB gold plus test)呈阳性。根据影像学和组织病理学检查结果,诊断为播散性结核病,累及淋巴结、肾脏、脾脏和肺部。THS是一种排除性诊断。该病例表明,根据ICHD-3标准诊断为THS的患者应进行全面评估,以排除诸如结核病等肉芽肿性感染。伴有肉芽肿性炎症的典型THS症状可能会让临床医生放松警惕,并阻碍对更危险病因的调查。由于疼痛性眼肌麻痹可继发于多种病理情况,在诊断THS之前应穷尽所有可能病因的诊断检查。无论MRI检查结果如何,都应完成结核病和真菌感染的检查。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3206/9873575/425ebe33e042/gr1.jpg

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