Tolosa-Hunt syndrome as initial presentation of Systemic Lupus Erythematosus.

Q3 Medicine
Acta neurologica Taiwanica Pub Date : 2021-03-01
Kang-Po Lee, Pi-Shan Sung, Wan-Ju Annabelle Lee
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引用次数: 0

Abstract

Purpose: Case presentation of newly diagnosed systemic lupus erythematosus (SLE) presenting initially as Tolosa-Hunt syndrome (THS).

Study design: Retrospective clinical case.

Method: Case report.

Results: A healthy young man developed acute binocular diplopia within 2 days without other neurological deficits. Bilateral 6th cranial nerve palsy was observed with general reduction in the visual field test. Emergent brain magnetic resonance image (MRI) was performed, which revealed severe inflammation in the cavernous sinus, superior orbital fissure, and apex of the orbit. No cavernous thrombosis or intracranial lesion was shown in the MRI. THS was diagnosed and the patient's CN 6 palsy recovered quickly after corticosteroid treatment. However, severe anaemia was discovered during admission (Hb=6.0), so the patient was evaluated by profound laboratory tests, which revealed SLE.

Conclusion: With painful ophthalmoplegia, cavernous sinus syndrome is highly suspected. THS is one of the differential diagnoses for cavernous sinus syndrome. THS is a rare disease, recognized by the National Organization for Rare Disorders, and characterized by inflammatory changes in the cavernous sinus, superior orbital fissure and/or orbital apex under image study. The inflammatory changes are mostly idiopathic, but secondary causes such as sarcoidosis or other autoimmune diseases need to be ruled out. Physicians should be aware of possible underlying conditions, such as immunosuppressed status as in SLE, as the true cause of THS.

Tolosa-Hunt综合征是系统性红斑狼疮的初始表现。
目的:新诊断的系统性红斑狼疮(SLE)的病例介绍,最初表现为Tolosa-Hunt综合征(THS)。研究设计:回顾性临床病例。方法:病例报告。结果:1例健康青年在2天内出现急性双眼复视,无其他神经功能缺损。双侧第6脑神经麻痹患者视野检查普遍缩小。急诊脑磁共振成像(MRI)显示海绵窦、眶上裂和眶尖严重炎症。MRI未见海绵体血栓形成或颅内病变。经皮质类固醇治疗后,患者CN 6麻痹迅速恢复。然而,入院时发现严重贫血(Hb=6.0),因此对患者进行了深入的实验室检查,结果为SLE。结论:海绵状窦综合征与疼痛性眼麻痹密切相关。这是海绵窦综合征的鉴别诊断之一。这是一种罕见的疾病,被美国国家罕见疾病组织认可,以海绵窦、眶上裂和/或眶尖的炎症改变为特征。炎症变化大多是特发性的,但继发性原因如结节病或其他自身免疫性疾病需要排除。医生应该意识到可能的潜在疾病,如SLE的免疫抑制状态,是三手烟的真正原因。
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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来源期刊
Acta neurologica Taiwanica
Acta neurologica Taiwanica Medicine-Neurology (clinical)
CiteScore
1.30
自引率
0.00%
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0
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