Department of Internal Medicine (Infectious Diseases), All India Institute of Medical Sciences, Jodhpur, 342005, India.
Department of Microbiology, Dr. S.N. Medical College, Jodhpur, India.
Orphanet J Rare Dis. 2023 Jun 2;18(1):133. doi: 10.1186/s13023-023-02744-z.
CNS actinomycosis is a rare chronic suppurative infection with non-specific clinical features. Diagnosis is difficult due to its similarity to malignancy, nocardiosis and other granulomatous diseases. This systematic review aimed to evaluate the epidemiology, clinical characteristics, diagnostic modalities and treatment outcomes in CNS actinomycosis.
The major electronic databases (PubMed, Google Scholar, and Scopus) were searched for the literature review by using distinct keywords: "CNS" or "intracranial" or "brain abscess" or "meningitis" OR "spinal" OR "epidural abscess" and "actinomycosis." All cases with CNS actinomycosis reported between January 1988 to March 2022 were included.
A total of 118 cases of CNS disease were included in the final analysis. The mean age of patients was 44 years, and a significant proportion was male (57%). Actinomycosis israelii was the most prevalent species (41.5%), followed by Actinomyces meyeri (22.6%). Disseminated disease was found in 19.5% of cases. Most commonly involved extra-CNS organs are lung (10.2%) and abdomen (5.1%). Brain abscess (55%) followed by leptomeningeal enhancement (22%) were the most common neuroimaging findings. Culture positivity was found in nearly half of the cases (53.4%). The overall case-fatality rate was 11%. Neurological sequelae were present in 22% of the patients. On multivariate analysis, patients who underwent surgery with antimicrobials had better survival (adjusted OR 0.14, 95% CI 0.04-0.28, p value 0.039) compared to those treated with antimicrobials alone.
CNS actinomycosis carries significant morbidity and mortality despite its indolent nature. Early aggressive surgery, along with prolonged antimicrobial treatment is vital to improve outcomes.
中枢神经系统放线菌病是一种罕见的慢性化脓性感染,具有非特异性的临床特征。由于其与恶性肿瘤、诺卡氏菌病和其他肉芽肿性疾病相似,因此诊断较为困难。本系统评价旨在评估中枢神经系统放线菌病的流行病学、临床特征、诊断方法和治疗结果。
使用不同的关键词,对主要电子数据库(PubMed、Google Scholar 和 Scopus)进行文献检索,检索词为:“CNS”或“颅内”或“脑脓肿”或“脑膜炎”或“脊髓”或“硬膜外脓肿”和“放线菌病”。纳入 1988 年 1 月至 2022 年 3 月期间报告的所有中枢神经系统放线菌病病例。
最终分析纳入了 118 例中枢神经系统疾病患者。患者的平均年龄为 44 岁,其中大部分为男性(57%)。最常见的病原体是以色列放线菌(41.5%),其次是迈耶放线菌(22.6%)。19.5%的病例存在播散性疾病。最常见的中枢神经系统外受累器官是肺(10.2%)和腹部(5.1%)。脑脓肿(55%)和软脑膜增强(22%)是最常见的神经影像学表现。近一半的病例(53.4%)培养阳性。总的病死率为 11%。22%的患者存在神经后遗症。多变量分析显示,与单独使用抗生素相比,接受手术联合抗生素治疗的患者生存状况更好(调整后的 OR 0.14,95%CI 0.04-0.28,p 值 0.039)。
尽管中枢神经系统放线菌病的性质较为惰性,但仍具有较高的发病率和死亡率。早期积极的手术联合延长的抗生素治疗对于改善预后至关重要。