Background and Purpose Guillain-Barre syndrome (GBS) is a common cause of inflammation-related acute flaccid paralysis, and is characterized by acute onset, rapid progression, and symmetrical weakness. GBS is an emergency with high morbidity and long-term disability rates. It is important to determine the prognostic factors for GBS in order to improve the disease outcomes. This study aimed to identify the correlation between the neutrophil-to-lymphocyte ratio (NLR) on day 1 of hospitalization (D1) and motor deterioration in GBS patients. Methods This observational analytical study applied a cross-sectional analysis to the medical records of GBS patients who were hospitalized at Dr. Soetomo General Hospital Surabaya from January 2018 to March 2020. The analysis used the chi-square bivariate test, multivariate analysis with logistic regression, and correlation analysis with the Spearman test. Results The study included 61 subjects. Statistical tests showed that there was no correlation between NLR and changes in the Medical Research Council sum scores (ΔMRC sum scores) during D1–D3, D1–D7, D1–D14, and D1 to the day of discharge ( p >0.05). There was a significant correlation between NLR and the Erasmus GBS outcome score (EGOS) ( p =0.006). NLR values differed significantly within each treatment group ( p =0.001). Therefore, a subanalysis within each treatment group was conducted, which revealed a significant negative correlation ( p <0.05) between NLR and the ΔMRC sum score during D1–D14 in the group treated without immunotherapy. Conclusions There was no correlation between NLR and motor deterioration in patients with GBS during hospitalization. However, NLR was significantly correlated with EGOS, and there was a negative correlation between NLR and motor deterioration during D1–D14 in GBS patients treated without immunotherapy.
Background: Guillain-Barré syndrome (GBS) is a peripheral nervous system inflammatory disease that is the most prevalent cause of acute flaccid paralysis, with an annual global incidence of 1-2 per 100,000 person-years. GBS typically appears with acute ascending flaccid paralysis and sensory abnormalities in anesthetic glove stockings; paralysis may extend to cranial muscles. Although the disease’s clinical presentation is diverse and there are multiple discrete clinical forms, myelopathy as a sign of GBS is a relatively unusual condition. Case presentation: GBS is diagnosed in a 29-year-old woman with myelopathy symptoms such as tetraparesis, hypoesthesia below the level of second thoracal myelum, aberrant proprioceptive in lower extremities, retention of urine and anhidrosis. We perform a lumbar puncture, and a cerebrospinal fluid (CSF) examination reveals albumin-cytological dissociation. Cervico-thoracic magnetic resonance imaging (MRI) revealed no abnormalities. Demyelinating polyradiculopathy was discovered using electromyography (EMG) and nerve conduction studies (NCS). Discussion: The classical presentation of GBS is progressive (ascending) limb weakness with decreased or absent physiological reflexes. Pharyngeal–cervical–brachial variation and face diplegia with paraesthesia are rare variations of GBS. Our patient presented with ascending limb weakness accompanied by a disturbance in the central nervous system but had similiar serological biomarker, which may be another rare variant of GBS. Conclusion: Diagnosis of GBS is quite challenging. GBS has a wide range of clinical symptoms. EMG-NCV and lumbar puncture are still required in myelopathic individuals with normal MRI, and unusual GBS symptoms should be explored. As a result, the choice of therapy and management becomes more appropriate.
Introduction: Lipomyelomeningocele is one of closed spinal dysraphism, inherently associated with tethered cord. Its prevalence ranges between 0.3 and 0.6 per 10.000 live births. Deterioration of bladder and bowel function often manifests before the motor and sensory function. Intraoperative neurophysiological monitoring (IONM) is often used in lipomyelomeningocele surgery to facilitate safe resection of lipomatous components and detethering of the spinal cord due to the absence of a clear boundary between the lipoma and neural placode.This case highlights the critical role of adequate IONM to reduce the complications of lipomyelomeningocele resection surgery. Case Presentation: Here we present a 10-year-old boy with a lump over the back since birth, progressively increased in size, and with a history of urinary and faecal incontinence since one year before admission. There was also hypoesthesia on lumbar 2 spinal cord level. Physical examination of the lumbosacral region revealed a single lump measured about 4.5 x 1.9 x 3.2 cm in size, soft consistency, and immobile. Magnetic resonance imaging of the lumbosacral region revealed a lipomyelomeningocele with tethered cord protruded into the anatomical defect from sacral vertebrae S1-S4. Surgery was indicated because of the neurological symptoms and it was safely performed with the assistance of IONM. There were no postoperative complications after surgery and there was an improvement in the patients' neurological symptoms. Conclusion: IONM in spinal surgery has been proven useful to reduce the postoperative neurological complication by providing identification of neural structures topographically and functionally, therefore, giving a warning alarm during surgery, which can be immediately responded by the surgeons.
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