Mazodier K, Bernit E, Faure V, Rovery C, Gayet S, Seux V, Donnet A, Brouqui P, Disdier P, Schleinitz N, Kaplanski G, Veit V, Harlé J-R
Service de médecine interne, CHU de la Conception, 147, boulevard Baille, 13385 cedex 05, Marseille, France.
Rev Med Interne. 2003 Feb;24(2):78-85. doi: 10.1016/s0248-8663(02)00715-4.
Tuberculosis involving the central nervous system (CNS) is rarely observed in non immuno-compromised hosts. We report herin the various clinical, biological and radiological manifestations observed in 7 patients with CNS tuberculosis.
Clinical and biological records of 7 patients with CNS tuberculosis were retrospectively studied. All patients had encephalic CT-scan and MRI in the course of the disease.
5 women and 2 men with a mean age of 38.4 years initially initially presented with headache (n = 6), fever (n = 5), meningeal irritation (n = 3), localizing neurological signs (n = 1). Lumbar punction revealed lymphocytic meningitis (n = 6/7). Mycobacterium tuberculosis or bovis was isolated in 3 patients only. Cerebral tomodensitography or magnetic resonance imaging were initially normal in most of cases (n = 4/7), but discovered in the course of disease basilar meningitis (n = 6), hydrocephalus (n = 6), abcess or tuberculoma (n = 4). In all the patients, initiation of the treatment was complicated by clinical and/or biological deterioration, called paradoxal reaction, leading in all cases to glucocorticoid adjunction, with various final results. Indeed, 4 patients developed neurological sequelae. No patient died.
CNS tuberculosis is a rare disease in non immunocompromised patients whose diagnostic may be difficult due to the absence of specific clinical symptoms, negative initial radiological examination, as well as delayed and often negative bacterial isolation. Paradoxal reaction appeared to be frequent despite specific antibiotherapy and underlines the beneficial effects of addictive corticosteroids.
中枢神经系统(CNS)结核在非免疫功能低下宿主中很少见。我们在此报告7例中枢神经系统结核患者观察到的各种临床、生物学和放射学表现。
对7例中枢神经系统结核患者的临床和生物学记录进行回顾性研究。所有患者在病程中均进行了脑部CT扫描和MRI检查。
5名女性和2名男性,平均年龄38.4岁,最初表现为头痛(n = 6)、发热(n = 5)、脑膜刺激征(n = 3)、定位性神经体征(n = 1)。腰椎穿刺显示淋巴细胞性脑膜炎(n = 6/7)。仅3例患者分离出结核分枝杆菌或牛分枝杆菌。大多数病例(n = 4/7)最初的脑密度测定或磁共振成像正常,但在病程中发现基底脑膜炎(n = 6)、脑积水(n = 6)、脓肿或结核瘤(n = 4)。所有患者在开始治疗时均出现临床和/或生物学恶化,称为矛盾反应,所有病例均导致加用糖皮质激素,最终结果各异。事实上,4例患者出现神经后遗症。无患者死亡。
中枢神经系统结核在非免疫功能低下患者中是一种罕见疾病,由于缺乏特异性临床症状、初始放射学检查阴性以及细菌分离延迟且常为阴性,其诊断可能困难。尽管进行了特异性抗微生物治疗,但矛盾反应似乎很常见,这突出了加用皮质类固醇的有益作用。