Department of Neurosurgery, University of Arizona College of Medicine, Phoenix, AZ, USA.
Department of Neurosurgery, University of Arizona College of Medicine, Phoenix, AZ, USA.
J Clin Neurosci. 2024 Nov;129:110850. doi: 10.1016/j.jocn.2024.110850. Epub 2024 Sep 28.
Harlequin syndrome (HS) is an uncommon condition affecting the sympathetic nervous system, characterized by asymmetrical flushing and sweating impairment, which can affect the face or half of the body. When the dysfunction results from external factors like damage or compression, it's referred to as Harlequin Sign. Our objective was to document an exceedingly rare presentation of Harlequin Sign caused by a T3-T4 paravertebral mass and conduct the first systematic literature review on this subject.
We conducted a systematic review of English-language studies using PubMed, Scopus, and Embase databases. We excluded abstracts, posters, congenital and idiopathic Harlequin Syndrome cases, as well as iatrogenic and secondary Harlequin Sign cases related to pathologies other than upper thoracic lesions.
We employed the PRISMA protocol and reviewed 1,538 papers, identifying 8 single case reports describing the Harlequin sign resulting from upper thoracic paravertebral lesions. The mean age of the patients was 41.25 years, with 6 (75 %) being female. The average time from onset to presentation was 8 months, and all patients (100 %) exhibited hemifacial flushing, while 4 (50 %) also had hemifacial anhidrosis. Stress or exercise exacerbated these symptoms in 50 % of cases. Additionally, 3 patients (37.5 %) presented with associated Horner Syndrome. The most commonly used diagnostic tool was a CT scan (50 %), revealing an average tumor diameter of 3.95 cm, with 50 % of cases located at T2-T3. Diagnosis indicated 57 % of cases as schwannomas and 29 % as lung adenocarcinoma (Superior Sulcus). Unfortunately, surgical treatment resolved symptoms in only 25 % of patients.
Hemifacial or hemibody autonomic symptoms should raise concern for paraspinal lesions in the thoracic spine. In addition to the first comprehensive review on this topic, we present a rare case of a T3/4 paraspinal schwannoma causing Harlequin Syndrome successfully managed with neurosurgical intervention.
哈勒昆综合征(HS)是一种罕见的影响交感神经系统的疾病,其特征为不对称性潮红和出汗障碍,可影响面部或半身。当功能障碍由损伤或压迫等外部因素引起时,称为哈勒昆征。我们的目的是记录一例由 T3-T4 椎旁肿块引起的极为罕见的哈勒昆征,并对该主题进行首次系统文献综述。
我们使用 PubMed、Scopus 和 Embase 数据库对英文文献进行了系统综述。我们排除了摘要、海报、先天性和特发性哈勒昆综合征病例,以及与上胸段病变以外的其他病理学相关的医源性和继发性哈勒昆征病例。
我们采用 PRISMA 方案,共查阅了 1538 篇论文,其中 8 篇个案报告描述了由上胸段椎旁病变引起的哈勒昆征。患者的平均年龄为 41.25 岁,其中 6 例(75%)为女性。从发病到就诊的平均时间为 8 个月,所有患者(100%)均出现半侧面部潮红,而 4 例(50%)还出现半侧无汗。50%的病例在应激或运动时会加重这些症状。此外,有 3 例(37.5%)患者出现伴随的霍纳综合征。最常用的诊断工具是 CT 扫描(50%),发现肿瘤平均直径为 3.95cm,50%的病例位于 T2-T3。诊断结果显示 57%的病例为神经鞘瘤,29%的病例为肺腺癌(Superior Sulcus)。不幸的是,手术治疗仅使 25%的患者症状得到缓解。
半侧或半身自主症状应引起对胸段脊柱旁病变的关注。除了对该主题的首次全面综述外,我们还报告了一例罕见的 T3/4 椎旁神经鞘瘤引起的哈勒昆综合征病例,经神经外科干预成功治疗。