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脊髓梅毒瘤:一种古老疾病的罕见表现。

Spinal Syphilitic Gumma: A Rare Presentation of an Old Disease.

作者信息

Worku Dominic, Houston Angela, Cosgrove Catherine, Byrne Laura

机构信息

Clinical Infection Unit, St. George's Hospital, BlackshawRoad, Tooting, London SW17 0QT, UK.

出版信息

Case Rep Infect Dis. 2021 Jun 2;2021:5533686. doi: 10.1155/2021/5533686. eCollection 2021.

Abstract

Syphilis is an ancient condition which still is of global concern today. Despite better awareness amongst clinicians and improving diagnostics, it remains likely underdiagnosed in part because of its namesake the 'great imitator.' While many patients suffer primary or secondary disease, tertiary syphilis characterised by gumma is rare, especially in the context of neurosyphilis. Here, we report a rare case of a well-controlled human immunodeficiency virus- (HIV-) positive gentleman with a history of previous syphilis and epilepsy who presented with progressive left leg weakness leading to immobility and altered bowels and, on neurological examination, Brown-Sequard syndrome. Magnetic resonance imaging (MRI) of the spine revealed two peripherally enhancing cavitating lesions at T4-T5 with associated meningeal thickening and cord oedema. Cerebrospinal fluid (CSF) analysis revealed high protein (3.07 g/dL) and white cell count (7 × 10/L) with negative cryptococcal antigen, tuberculosis molecular testing (GeneXpert), microscopy and culture, and viral polymerase chain reaction (PCR). CSF serology was positive for particle agglutination (TPPA) 10240 and RPR 1 in 2 suggesting active disease. While TB treatment had been started prior to these investigations on day 11, 14-day high-dose benzylpenicillin therapy commenced. Repeat MRI of the spine at days 12 and 22 showed incremental improvements in all parameters which correlated with improving functionality and neurology. According to our literature search, this represents the 13 case recorded for spinal syphilitic gumma and the only case recorded in a HIV-positive individual and adds to the evidence that, in the absence of rapidly changing neurology, medical management can lead to good clinical outcomes.

摘要

梅毒是一种古老的疾病,如今仍受到全球关注。尽管临床医生的认识有所提高,诊断方法也在不断改进,但它可能仍存在诊断不足的情况,部分原因在于其绰号“伟大的模仿者”。虽然许多患者患有一期或二期梅毒,但以梅毒瘤为特征的三期梅毒很少见,尤其是在神经梅毒的情况下。在此,我们报告一例罕见病例,一名人类免疫缺陷病毒(HIV)阳性且病情得到良好控制的男性,有梅毒和癫痫病史,出现进行性左腿无力,导致无法行走,并伴有肠道功能改变,经神经检查诊断为布朗 - 塞卡尔综合征。脊柱磁共振成像(MRI)显示T4 - T5水平有两个周边强化的空洞性病变,伴有脑膜增厚和脊髓水肿。脑脊液(CSF)分析显示蛋白含量高(3.07 g/dL),白细胞计数高(7×10/L),隐球菌抗原、结核分子检测(GeneXpert)、显微镜检查和培养以及病毒聚合酶链反应(PCR)均为阴性。脑脊液血清学检测颗粒凝集试验(TPPA)为10240阳性,快速血浆反应素环状卡片试验(RPR)为1:2阳性,提示疾病处于活动期。在这些检查之前的第11天已开始进行结核病治疗,同时开始了为期14天的大剂量苄星青霉素治疗。在第12天和第22天重复进行的脊柱MRI显示所有参数都有逐步改善,这与功能和神经学状况的改善相关。根据我们的文献检索,这是记录在案的第13例脊髓梅毒瘤病例,也是唯一一例记录在HIV阳性个体中的病例,进一步证明了在没有快速变化的神经学症状的情况下,药物治疗可带来良好的临床结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41ec/8192201/ee678a467d66/CRIID2021-5533686.001.jpg

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