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[梅毒性葡萄膜炎的临床及临床旁特征]

[Clinical and paraclinical features of syphilitic uveitis].

作者信息

Marty A-S, Cornut P-L, Janin-Manificat H, Perard L, Debats F, Burillon C

机构信息

Service d'ophtalmologie, hôpital Édouard-Herriot, 5, place d'Arsonval, 69003, Lyon, France.

Centre ophtalmologique pôle vision, clinique du Val-d'ouest, 39, chemin de la Vernique, 69130, Écully, France.

出版信息

J Fr Ophtalmol. 2015 Mar;38(3):220-8. doi: 10.1016/j.jfo.2014.09.011. Epub 2015 Jan 28.

Abstract

INTRODUCTION

Syphilis, caused by Treponema pallidum agent, results in polymorphic and non-specific ocular manifestations. Early diagnosis and institution of individualized treatment play a large role in the prognosis. The increase in syphilis over the past several years requires the ophthalmologist to consider this diagnosis in the setting of any intraocular inflammatory involvement.

PURPOSE

To describe epidemiological, clinical and paraclinical features and natural history of syphilitic uveitis.

MATERIALS AND METHODS

Retrospective, descriptive and non-comparative study of a series of patients hospitalized between 2007 and 2013 in our department of ophthalmology for management of ocular inflammation associated with a positive syphilitic serology.

RESULTS

Thirteen patients of mean age 52.5 years ± 12.9 (33-82 years) were included. All were male and were followed for six months. Co-infection with human immunodeficiency virus (HIV) was present in four of them. Other risk factors discovered on history were unprotected sexual relations, multiple partners, homosexual relations, co-infection with another sexually transmitted disease (STD) or an occupational risk. Decreased visual acuity (VA) was present in all patients, with an average initial VA of 0.71 ± 0.81 LogMAR, i.e. 2/10. Involvement was bilateral in 38% (n=5) of cases. Papilledema was present in 10 patients. Seven patients exhibited vasculitis, 6 patients a necrotizing retinitis, 2 patients with placoid lesions, 7 patients with panuveitis and 2 patients with macular edema. We did not find any patients with isolated anterior uveitis. Three patients exhibited concomitant extraocular involvement with cutaneous palmoplantar lesions. Spectral domain optical coherence tomography (SD-OCT) found a fragmentation of the external limiting membrane and a disorganization of the ellipsoid line in two patients. Cerebrospinal fluid was studied for all patients. Eight of them exhibited lymphocytic meningitis, and we found the presence of anti-Treponema pallidum hemagglutination assay antibody (TPHA) in 9 patients and anti-veneral disease research laboratory antibody (VDRL) in 1 patient. Syphilis polymerase chain reaction (PCR) in the aqueous humor was positive in 50% (n=6) of studied cases and the PCR for Epstein Barr virus came back positive in four specimens out of eight. False positive reactions were observed for Lyme disease in eight patients. The four HIV-positive patients showed bilateral lesions more frequently, but less severe and with a favorable outcome. Antibiotic treatment with ceftriaxone (2 grams per day intramuscularly for 15 to 21 days) and local treatment (corticoids and mydriatics) in the case of inflammation of the anterior segment, allowed a regression of the inflammation in all of our patients as well as an improvement in VA (average final VA 0.09 ± 0.17 LogMAR, i.e. approximately 8/10). One Jarisch Herxheimer reaction occurred and was resolved with systemic corticosteroid therapy. A change in the retinal pigment epithelium was the main sequela in 44% of cases (n=8 eyes).

CONCLUSION

Every structure of the eye may be involved with syphilis; therefore, syphilis must be systematically sought during the etiologic assessment of ocular inflammation even in the absence of historical risk factors. HIV-positive patients must be handled in the same way as immunocompetent patients. Collaboration with the internist is essential for the diagnosis, monitoring, and staging, especially in search of neurosyphilis. The clinical course is favorable with early treatment.

摘要

引言

梅毒由苍白密螺旋体引起,可导致多种形态且非特异性的眼部表现。早期诊断和个体化治疗对预后起着重要作用。过去几年梅毒发病率的上升要求眼科医生在任何眼内炎症受累的情况下都要考虑这一诊断。

目的

描述梅毒性葡萄膜炎的流行病学、临床和辅助检查特征以及自然病程。

材料与方法

对2007年至2013年在我们眼科住院治疗与梅毒血清学阳性相关的眼部炎症的一系列患者进行回顾性、描述性和非对照研究。

结果

纳入13例平均年龄为52.5岁±12.9岁(33 - 82岁)的患者。所有患者均为男性,随访6个月。其中4例合并人类免疫缺陷病毒(HIV)感染。病史中发现的其他危险因素包括无保护性行为、多个性伴侣、同性恋关系、合并另一种性传播疾病(STD)或职业风险。所有患者均有视力下降,初始平均视力为0.71±0.81 LogMAR,即2/10。38%(n = 5)的病例为双侧受累。10例患者出现视乳头水肿。7例患者表现为血管炎,6例患者为坏死性视网膜炎,2例患者有地图状病灶,7例患者为全葡萄膜炎,2例患者有黄斑水肿。未发现单纯前葡萄膜炎患者。3例患者伴有眼外皮肤掌跖病变。光谱域光学相干断层扫描(SD - OCT)在2例患者中发现外限制膜破碎和椭圆体线紊乱。对所有患者进行了脑脊液检查。其中8例表现为淋巴细胞性脑膜炎,9例患者检测到抗梅毒螺旋体血凝试验抗体(TPHA)阳性,1例患者检测到抗性病研究实验室抗体(VDRL)阳性。房水梅毒聚合酶链反应(PCR)在50%(n = 6)的研究病例中呈阳性,8份标本中有4份爱泼斯坦 - 巴尔病毒PCR呈阳性。8例患者莱姆病检测出现假阳性反应。4例HIV阳性患者双侧病变更常见,但病情较轻且预后良好。对于前段炎症患者,采用头孢曲松(每天2克肌肉注射,共15至21天)进行抗生素治疗以及局部治疗(使用皮质类固醇和散瞳剂),使所有患者炎症消退且视力提高(最终平均视力0.09±0.17 LogMAR,即约8/10)。发生1例赫氏反应,经全身皮质类固醇治疗后缓解。44%(n = 8只眼)的病例主要后遗症为视网膜色素上皮改变。

结论

眼的每个结构都可能受累于梅毒;因此即使没有病史危险因素,在眼部炎症的病因评估中也必须系统地排查梅毒。HIV阳性患者的处理方式应与免疫功能正常患者相同。与内科医生合作对于诊断、监测和分期至关重要,尤其是在排查神经梅毒时。早期治疗临床病程良好。

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