Nasiri Jafar, Ghazavi Mohamadreza, Yaghini Omid, Chaldavi Mohamad
Department of Pediatric Neurology, Faculty of Medicine, Child Growth and Development Research Center, Isfahan University of Medical Sciences, Isfahan, Iran.
Iran J Child Neurol. 2018 Spring;12(2):49-57.
There are no reports about the clinical presentations and outcome of Guillain-Barré syndrome (GBS) in our region, therefore, we aimed to report some mentioned findings in children diagnosed with GBS in Isfahan, central Iran.
MATERIALS & METHODS: In this retrospective study, pediatric diagnosed with GBS referred to Imam Hossein Hospital, the Pediatric Referral Center of Isfahan Province, central Iran were enrolled from 2011-2014. The following data were extracted from the medical files of patients; age, gender, early signs and symptoms of GBS, neurological features, sensory and motor and autonomic involvements, sphincter dysfunction, bulbar muscle involvement, respiratory failure, cranial nerve paralysis, delay time from onset to definite diagnosis and management of GBS and the outcome.
Overall, 57 children with GBS aged 1-13 yr were evaluated. Frequency of GBS was significantly higher in boys than in girls (38.6% vs. 61.4%, =0.01, OR=0.39). The most common clinical presentations were distal lower limb weakness (92.11%), reduced deep tendon reflex (DTR) (82.46%) and neuropathic pain (75.44%). 92.9% of patients had complete recovery.
Distal lower limb weakness, reduced deep tendon reflex, and neuropathic pain are the main clinical presentation in children with GBS but in some patients, DTR may be normal or even exaggerated in early stage of disease. Revising the diagnostic criteria for GBS may be necessary. Most of our patients had complete recovery. The only death was due to autonomic involvement. Autonomic dysfunction could be associated with catastrophic outcome and patients with these clinical presentations need critical care.
我们所在地区尚无关于吉兰 - 巴雷综合征(GBS)临床表现及预后的报道,因此,我们旨在报告伊朗中部伊斯法罕被诊断为GBS的儿童的上述相关发现。
在这项回顾性研究中,纳入了2011年至2014年转诊至伊朗中部伊斯法罕省儿科转诊中心伊玛目侯赛因医院且被诊断为GBS的儿童。从患者的医疗档案中提取以下数据:年龄、性别、GBS的早期体征和症状、神经学特征、感觉、运动及自主神经受累情况、括约肌功能障碍、延髓肌受累情况、呼吸衰竭、脑神经麻痹、从发病到明确诊断及GBS治疗的延迟时间以及预后。
总体而言,评估了57例年龄在1至13岁的GBS儿童。GBS在男孩中的发病率显著高于女孩(38.6%对61.4%,P = 0.01,OR = 0.39)。最常见的临床表现为下肢远端无力(92.11%)、腱反射减弱(DTR)(82.46%)和神经性疼痛(75.44%)。92.9%的患者完全康复。
下肢远端无力、腱反射减弱和神经性疼痛是GBS患儿的主要临床表现,但在某些患者中,疾病早期DTR可能正常甚至亢进。可能有必要修订GBS的诊断标准。我们的大多数患者完全康复。唯一的死亡是由于自主神经受累。自主神经功能障碍可能与灾难性后果相关,有这些临床表现的患者需要重症监护。