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布氏杆菌性脑膜炎的流行病学、临床和实验室特征。

Epidemiological, clinical, and laboratory features of brucellar meningitis.

机构信息

Department of Public Health, School of Health, Shahid Beheshti University of Medical Sciences, Daneshjoo Blvd., Tabnak St., Evin, Tehran, Iran.

出版信息

Arch Iran Med. 2010 Nov;13(6):486-91.

Abstract

BACKGROUND

One of the rare complications of brucellosis is mononuclear meningitis, which usually imitates systemic disease.

METHODS

Documents of patients with confirmed brucellar meningitis hospitalized in Sina Hospital (Western Iran) between 1988-2005 were collected.

RESULTS

The average age was 26.9. 64% were female and 36% were male. There were 25% confirmed cases in the spring, 21% in summer, 33% in autumn and 21% in winter.Patient complaints in order of frequency were: headache (95%), vomiting (77%), fatigue (39%), myalgia (15%), movement disorders (15%), arthralgia (13%), sleepiness (13%), and aphasia (3%). The main clinical findings were: nuchal rigidity (74%), splenomegaly (49%), fever (41%), Kernig's (41%), and Brudzinski's signs (39%). Leukopenia (WBC<4.5×109/L; 18%), leukocytosis (WBC>9.5×109/L; 20%), and anemia (hemoglobin level<13 g/dL in men and 12 g/dL in women) were detected in 16% of patients. The Wright agglutination test, with a titer of 1:80 to 1:1280 was present in the serum of all patients, CSF Wright test or Coombs test was positive in half of the patients. Blood, bone marrow and CSF cultures were positive in 6 out of 10 patients.

DISCUSSION

The epidemiological aspects of brucellar meningitis are similar to systemic brucellosis and, in most studies; there is no significant difference between them. The sex distribution of patients was different from most studies. Seasonal distribution of the disease did not follow seasonal distribution of systemic brucellosis, however, clinical findings or laboratory changes were similar to Turkey and other studies in Iran. A definite response, without complications and next recurrence, in this study, was achieved with co-trimoxasole plus rifampin for 45 days of therapy.

摘要

背景

布鲁氏菌病的罕见并发症之一是单核细胞性脑膜炎,通常类似于全身疾病。

方法

收集了 1988 年至 2005 年期间在锡纳医院(伊朗西部)住院的确诊布鲁氏菌性脑膜炎患者的文献。

结果

平均年龄为 26.9 岁。64%为女性,36%为男性。春季确诊病例占 25%,夏季占 21%,秋季占 33%,冬季占 21%。患者的主诉按频率排列如下:头痛(95%)、呕吐(77%)、疲劳(39%)、肌痛(15%)、运动障碍(15%)、关节炎(13%)、嗜睡(13%)和失语(3%)。主要的临床发现是:颈项强直(74%)、脾肿大(49%)、发热(41%)、克尼格征(41%)和布鲁津斯基征(39%)。白细胞减少症(白细胞<4.5×109/L;18%)、白细胞增多症(白细胞>9.5×109/L;20%)和贫血(男性血红蛋白水平<13 g/dL,女性血红蛋白水平<12 g/dL)在 16%的患者中检测到。所有患者的血清中均存在 1:80 至 1:1280 的 Wright 凝集试验,半数患者的 CSF Wright 试验或 Coombs 试验阳性。10 例患者中有 6 例血液、骨髓和 CSF 培养阳性。

讨论

布鲁氏菌性脑膜炎的流行病学与全身布鲁氏菌病相似,在大多数研究中,两者之间无显著差异。患者的性别分布与大多数研究不同。疾病的季节性分布与全身布鲁氏菌病的季节性分布不同,但临床发现或实验室变化与土耳其和伊朗的其他研究相似。在本研究中,采用复方新诺明联合利福平治疗 45 天,达到了无并发症和无复发的明确疗效。

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