Aphagia Strongly Suspected to Be Caused by an Allergic Reaction to a Gelatin-based Hemostatic Agent after Anterior Cervical Decompression and Fusion for Central Cervical Cord Injury.

NMC Case Report Journal Pub Date : 2022-06-21 eCollection Date: 2022-01-01 DOI:10.2176/jns-nmc.2022-0017
Satoshi Tanaka, Ryosuke Tomio, Norihiko Akao, Tsunemasa Shimizu, Toshio Ishikawa, Takeshi Fujimoto, Terumasa Nishimatsu
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Abstract

Gelatin-based hemostatic agents are widely used in neurosurgery. This is a case of postoperative aphagia strongly suspected to be caused by an allergic reaction to a gelatin-based hemostatic agent after anterior cervical decompression and fusion for central cervical cord injury. A 55-year-old man underwent cervical anterior decompression and fusion at the C3/4 and 4/5 levels for central cervical cord injury. Immediately after the surgery, he could not swallow saliva at all, but his voice was not hoarse. Postoperative cervical computed tomography and magnetic resonance imaging showed significant edema from the post-hypopharynx wall to the front of the vertebral body. The retropharyngeal space was remarkably enlarged to 15.8 mm with cervical spine X-rays. Without neurological symptom improvement, his condition was diagnosed as marked edema of the area where Surgiflo (porcine-derived gelatin-based hemostatic agent; Johnson & Johnson Wound Management, Somerville, NJ, USA) had been applied during the operation. It was strongly suspected to be caused by an allergic response to the porcine-derived gelatin. When methylprednisolone 1000 mg was administered for 3 days from the 5th postoperative day, swallowing became almost normal within a few hours after the initial administration, and his neurological symptoms improved. The patient left the hospital on the 12th day after the operation. Before using porcine-derived gelatin products during surgery, special consideration should be given to patients with an allergy history before surgery.

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失语症强烈怀疑是由于对明胶止血剂的过敏反应引起的颈椎前路减压融合治疗中心性脊髓损伤。
明胶类止血剂广泛应用于神经外科。这是一例术后失语症,强烈怀疑是由于前路颈椎减压融合治疗中心性颈髓损伤后对明胶止血剂的过敏反应引起的。55岁男性因中心性颈髓损伤行颈椎前路减压和C3/4和4/5节段融合术。手术后,他完全无法吞咽唾液,但声音并不沙哑。术后颈椎计算机断层扫描和磁共振成像显示从下咽后壁到椎体前部明显水肿。颈椎x线片显示咽后间隙明显增大至15.8 mm。神经系统症状没有改善,他的病情被诊断为Surgiflo(猪源明胶止血剂;强生伤口管理公司(美国新泽西州萨默维尔)在手术中应用。人们强烈怀疑这是由对猪源明胶的过敏反应引起的。术后第5天起给予甲强的松龙1000 mg,连续3天,术后数小时吞咽基本恢复正常,神经系统症状改善。患者于术后第12天出院。在手术中使用猪源明胶产品之前,应特别考虑术前有过敏史的患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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