POLYRADICULONEURITIS IN AN ADOLESCENT AFTER ACUTE PNEUMONIA

Teodora Jescu, I. Miron, V. Lupu, Ș. Moisă, Anca-Lavinia Postolache, O. Miron, Ancuța Lupu
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Abstract

Polyradiculoneuritis or Guillan Barré’s Syndrome is the most common cause of acute and subacute generalized paralysis, which is likely to occur at any age. We present the case of a 17-year-old adolescent who was admitted to our clinic for swallowing and phonation disorders, evolving into acute respiratory insufficiency (which required orotracheal intubation and ventilatory support), hypotonia in the upper and lower limbs, and globally-decreased osteotendinous reflexes, abolished in the upper limbs. The thoraco-abdominal X-ray and the chest CT revealed lower respiratory infection, and the neurological clinical examination and the lumbar puncture with albino-cytological dissociation raised the suspicion of polyradiculoneuritis. Therapy with intravenous immunoglobulin resulted in the improvement of the motor deficiency, but without the possibility to detubate the patient. Following 2 sessions of plasmapheresis with 20% human albumin, significant improvement of the neurological deficiency was seen and spontaneous breathing was resumed, the patient regaining full muscle strength.
青少年急性肺炎后的多根神经炎
多根神经炎或Guillan barr综合征是急性和亚急性全身性麻痹的最常见原因,这可能发生在任何年龄。我们报告一名17岁的青少年因吞咽和发声障碍而入院,后来发展为急性呼吸功能不全(需要经气管插管和通气支持),上肢和下肢张力低下,上肢骨腱反射全面下降,上肢完全消失。胸腹x线及胸部CT示下呼吸道感染,神经学临床检查及腰椎穿刺伴白化细胞学分离提示多根神经炎怀疑。静脉注射免疫球蛋白治疗导致运动缺陷的改善,但没有可能辩论病人。在用20%人白蛋白进行2次血浆置换治疗后,神经功能缺陷明显改善,恢复了自主呼吸,患者恢复了完全的肌肉力量。
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