A rare case of postoperative pain in congenital analgesia: case report

André Lavor Alves, Flávio Lobo Maia, Washington Aspilicueta Pinto Filho Pinto Filho, João Manuel Figueira da Silva, Joaquim Trajano de Lima Filho
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引用次数: 0

Abstract

Objective: we describe a case of a patient with familial dysautonomia and postoperative pain. Methodology: clinical follow-up for 10 years in a tertiary pediatric hospital. Results: it is a 12 years old teenager, diagnosed with Riley-Day Syndrome, after undergoing various orthopedic surgical procedures, evolves with changes in pain perception, in systematic assessments. Conclusion: Family Disautonomy is one of the most common Hereditary Sensory and Autonomic Neuropathies (HSAN). Children gradually evolve with sensory changes, leading to a progressive decrease in pain perception. In addition, spinal deformities and recurrent orthopedic trauma can occur. The reported patient presents, contradictorily, an increase in the perception of pain and allodynia after undergoing repetitive orthopedic procedures.
先天性镇痛术后疼痛1例报告
目的:我们描述了一例家族性自主神经异常和术后疼痛的患者。方法:在某三级儿科医院进行10年临床随访。结果:该患者为12岁青少年,经各种骨科手术后诊断为Riley-Day综合征,在系统评估中随着疼痛感知的改变而发展。结论:家族自主性障碍是最常见的遗传性感觉和自主神经病变(HSAN)之一。儿童的感觉逐渐发生变化,导致疼痛感知能力逐渐下降。此外,脊柱畸形和复发性骨科创伤也可能发生。报告的患者,矛盾的是,在接受重复性矫形手术后,疼痛和异常性疼痛的感觉增加。
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16 weeks
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