Nazari Ryan, Hall Jonathan C
College of Osteopathic Medicine, Kansas City University, Kansas City, USA.
Department of Internal Medicine, Overland Park Regional Medical Center, Overland Park, USA.
Cureus. 2025 Jun 17;17(6):e86213. doi: 10.7759/cureus.86213. eCollection 2025 Jun.
Guillan-Barré syndrome (GBS) is an autoimmune-mediated process that typically causes a progressive ascending paralysis that can lead to persistence of symptoms, permanent paralysis, and even death. While most cases follow a classical course with gradual progression of symptoms until eventual plateau, atypical and rapid onset clinical presentations can complicate differential diagnosis and diagnostic certainty, leading to late diagnosis by clinicians. A 35-year-old male with a history of intravenous (IV) methamphetamine use presented with a sudden onset and complete motor and sensory triplegia of the bilateral legs and left arm upon waking, which resolved shortly after hospital admission. After transfer for neurological referral, his only complaint of distal extremity paresthesia improved daily until hospital day 3, in which he experienced acute quadriplegia with complete sensory and motor loss, prompting stroke protocol activation. Neuroimaging was unremarkable, but cerebrospinal fluid (CSF) analysis revealed elevated protein (87.3 mg/dL) with albuminocytologic dissociation (ACD). The patient was subsequently initiated on intravenous immunoglobulin (IVIg); however, his symptoms had almost completely resolved prior to the initiation of this treatment. He ultimately experienced full recovery without residual deficits. This case highlights a rare and diagnostically challenging presentation of suspected GBS, marked by transient and recurrent neurologic deficits rather than the classic monophasic presentation. Such presentations may be mistaken for functional disorders or overlooked entirely, delaying appropriate neurological evaluation. Despite rapid resolution of symptoms and other possible underlying etiologies in this case, hallmark CSF findings of elevated protein and ACD supported the diagnosis. This underscores the importance of maintaining a high index of suspicion for GBS in patients with unexplained neurological deficits, especially in the context of a recent illness. Early recognition remains critical to guide management and prevent severe complications.
吉兰-巴雷综合征(GBS)是一种自身免疫介导的疾病,通常会导致进行性上升性麻痹,可导致症状持续、永久性麻痹甚至死亡。虽然大多数病例遵循典型病程,症状逐渐进展直至最终稳定,但非典型和快速起病的临床表现会使鉴别诊断和诊断确定性复杂化,导致临床医生诊断延迟。一名有静脉注射甲基苯丙胺病史的35岁男性醒来后突然出现双侧下肢和左臂完全性运动和感觉性三肢瘫,入院后不久症状缓解。转诊至神经科后,他唯一的远端肢体感觉异常主诉每天都在改善,直到住院第3天,他出现急性四肢瘫,伴有完全性感觉和运动丧失,促使启动卒中诊疗方案。神经影像学检查无异常,但脑脊液(CSF)分析显示蛋白升高(87.3mg/dL)伴蛋白细胞分离(ACD)。随后该患者开始接受静脉注射免疫球蛋白(IVIg)治疗;然而,在开始这种治疗之前,他的症状几乎已完全缓解。他最终完全康复,没有遗留缺陷。该病例突出了疑似GBS的一种罕见且具有诊断挑战性的表现,其特征为短暂性和复发性神经功能缺损,而非典型的单相表现。此类表现可能被误诊为功能性障碍或完全被忽视,从而延误适当 的神经学评估。尽管该病例症状迅速缓解且可能存在其他潜在病因,但脑脊液中蛋白升高和蛋白细胞分离的典型表现支持了诊断。这强调了对不明原因神经功能缺损患者,尤其是近期患病背景下的患者,保持高度怀疑GBS的重要性。早期识别对于指导治疗和预防严重并发症仍然至关重要。