Ghosh Ritwik, Mandal Arpan, León-Ruiz Moisés, Roy Dipayan, Das Shambaditya, Dubey Souvik, Benito-León Julián
Department of General Medicine, Burdwan Medical College and Hospital, Burdwan, West Bengal, India.
Section of Clinical Neurophysiology, Department of Neurology, University Hospital "La Paz", Madrid, Spain.
Neurologia (Engl Ed). 2024 Nov-Dec;39(9):766-780. doi: 10.1016/j.nrleng.2022.07.001. Epub 2022 Jul 28.
Scrub typhus is a potentially life-threatening but curable disease that can produce multi-organ failure. Neurological manifestations in scrub typhus have gained attention recently, where the entire neural axis except the myoneural junction can be involved. Although the pathogenesis of neurological involvement has not been established, immune-mediated mechanisms are suspected. This article reports the clinicopathological features of scrub typhus cases presenting several rare neurological and neuropsychiatric manifestations.
Three hundred fifty-four serologically confirmed scrub typhus cases were admitted to the Department of General Medicine of Burdwan Medical College and Hospital (West Bengal, India) between May 2018 and May 2022. There were 50 patients who had predominantly neurological manifestations. Of these 50 cases, ten patients presented with extremely rare neurological manifestations.
We report 10 cases of scrub typhus (four men and six women) who presented with complex neurological pictures (posterior reversible encephalopathy syndrome, Opalski syndrome, parkinsonism, cerebellitis, isolated opsoclonus, acute transverse myelitis, myositis, polyradiculoneuropathy with cranial neuropathy, acute transient behavioral changes, and fibromyalgia). Immune-mediated mechanisms might have mediated the pathogenesis of most cases following scrub typhus infection.
From a clinicopathological point of view, each case was unique in its presentation and treatment response. In any acute onset neurological disorders associated with febrile illness in the tropics or subtropics, scrub typhus infection should be included in the differential diagnosis, despite the absence of eschar and unremarkable neuroimaging findings. This otherwise curable disease may result in multi-organ dysfunction syndrome and death if the diagnosis is delayed.
恙虫病是一种可能危及生命但可治愈的疾病,可导致多器官功能衰竭。恙虫病的神经表现最近受到关注,除了肌神经接头外,整个神经轴均可受累。尽管神经受累的发病机制尚未明确,但怀疑是免疫介导的机制。本文报告了出现几种罕见神经和神经精神表现的恙虫病病例的临床病理特征。
2018年5月至2022年5月期间,354例血清学确诊的恙虫病病例被收治到布尔万医学院和医院(印度西孟加拉邦)普通内科。有50例患者主要表现为神经症状。在这50例病例中,有10例出现极其罕见的神经表现。
我们报告了10例恙虫病病例(4名男性和6名女性)表现出复杂的神经症状(后部可逆性脑病综合征、奥帕尔斯基综合征、帕金森症、小脑炎、孤立性眼阵挛、急性横贯性脊髓炎、肌炎、伴有颅神经病变的多神经根神经病、急性短暂行为改变和纤维肌痛)。免疫介导的机制可能介导了大多数恙虫病感染后病例的发病过程。
从临床病理角度来看,每个病例在表现和治疗反应方面都是独特的。在热带或亚热带地区,任何与发热性疾病相关的急性起病的神经疾病,尽管没有焦痂且神经影像学检查结果不明显,也应将恙虫病感染纳入鉴别诊断。这种原本可治愈的疾病如果诊断延迟,可能会导致多器官功能障碍综合征和死亡。