Alanazi Ali, Al Najjar Sara, Madkhali Jnadi, Al Malik Yaser, Al-Khalaf Athal, Alharbi Ahmad
Division of Neurology, King Abdulaziz Medical City, Ministry of the National Guard-Health Affairs, Riyadh 11426, Saudi Arabia.
College of Medicine, King Saud bin Abdulaziz University for Health Sciences, Riyadh 14611, Saudi Arabia.
Infect Dis Rep. 2021 Jan 1;13(1):1-10. doi: 10.3390/idr13010001.
Brucellosis is a zoonotic disease that can affect the central and peripheral nervous system and it has variable neurological manifestation. However, brucellosis infection that presents with acute peripheral neuropathy mimicking Guillain-Barre syndrome (GBS) is rarely reported in the literature.
We report a 56-year-old man who was initially diagnosed with GBS, and then he was confirmed to have acute infection. We also did a systematic literature review to study the natural history and management of previously reported cases of brucellosis that presented with manifestations consistent with GBS.
We found 19 (including our patient) cases of brucellosis that presented with GBS-like manifestations. The age range was 9-62 years. Eight (42.1%) patients had a history of fever. Seven (36.8%) patients had no constitutional symptoms. Five (26.3%) patients had splenomegaly. serological tests were positive in all patients, while blood culture was positive in three (37.5%) out of eight patients. Albuminocytological dissociation was present in nine (64.3%) out of 14 patients. Nerve conduction studies and electromyography were consistent with demyelination polyneuropathy in eight (42.1%) patients, with axonal polyneuropathy in six (31.6) patients, and with mixed axonal and demyelinating polyneuropathy in one (5.3%) patient. Spine MRI showed root enhancement in three (42.9%) patients.
In regions endemic with brucellosis, acute peripheral neuropathy presentation may warrant investigations for infection.
布鲁氏菌病是一种人畜共患疾病,可影响中枢和周围神经系统,且有多种神经学表现。然而,文献中很少报道布鲁氏菌病感染表现为类似吉兰 - 巴雷综合征(GBS)的急性周围神经病变。
我们报告一名56岁男性,最初被诊断为GBS,随后确诊为急性布鲁氏菌病感染。我们还进行了系统的文献综述,以研究先前报道的表现与GBS一致的布鲁氏菌病病例的自然病史和治疗方法。
我们发现19例(包括我们的患者)布鲁氏菌病表现为类似GBS的症状。年龄范围为9至62岁。8例(42.1%)患者有发热史。7例(36.8%)患者无全身症状。5例(26.3%)患者有脾肿大。所有患者血清学检查均呈阳性,而8例患者中有3例(37.5%)血培养呈阳性。14例患者中有9例(64.3%)出现蛋白细胞分离现象。神经传导研究和肌电图显示,8例(42.1%)患者符合脱髓鞘性多发性神经病,6例(31.6%)患者符合轴索性多发性神经病,1例(5.3%)患者符合轴索与脱髓鞘混合性多发性神经病。脊柱磁共振成像显示3例(42.9%)患者神经根强化。
在布鲁氏菌病流行地区,急性周围神经病变表现可能需要对布鲁氏菌病感染进行调查。