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青少年患者的休曼氏胸椎后凸畸形

Scheuermann's thoracic kyphosis in the adolescent patient.

作者信息

Hart Erin S, Merlin Gabriel, Harisiades Jamie, Grottkau Brian E

机构信息

Department of Orthopaedic Surgery, Yawkey Center for Outpatient Care, Massachusetts General Hospital for Children, Boston, MA, USA.

出版信息

Orthop Nurs. 2010 Nov-Dec;29(6):365-71; quiz 372-3. doi: 10.1097/NOR.0b013e3181f83761.

Abstract

Scheuermann's thoracic kyphosis is a condition characterized by increased posterior rounding of the thoracic spine in association with structural deformity of the vertebral elements. It is a structural deformity of the spine that is classically characterized by anterior wedging of 5° or more of 3 adjacent thoracic vertebral bodies with kyphosis measuring greater than 45° between T5 and T12. The cause of the deformity remains unknown but it is believed to be multifactorial, and it likely has a genetic component as well. Most adolescent patients seek orthopaedic evaluation for increased rounding and deformity of the thoracic spine that is occasionally associated with back pain. Parental concerns are also often related to the cosmetic deformity and the progressive nature of the condition. Bracing has been demonstrated to be an effective nonsurgical treatment modality for the skeletally immature child and/or adolescent with a progressive deformity. Operative management has been advocated for adolescents with progressive kyphosis measuring over 70°, for those who have had progression despite bracing, for patients with intractable back pain, and also for patients with unacceptable cosmetic deformity. Surgical options include posterior spinal arthrodesis with or without anterior spinal release via thoractomy or video-assisted thoracoscopic surgery (VATS). This article will review the diagnosis, pathophysiology, physical examination findings, and the nonoperative and surgical treatment options for adolescent patients with Scheuermann's kyphosis of the thoracic spine.

摘要

休曼氏胸椎后凸是一种以胸椎后凸增加并伴有椎体结构畸形为特征的病症。它是一种脊柱结构畸形,典型特征为3个相邻胸椎椎体前缘楔形变5°或更多,且T5至T12之间的后凸角度大于45°。该畸形的病因尚不清楚,但被认为是多因素的,可能也有遗传因素。大多数青少年患者因胸椎后凸增加和畸形前来接受骨科评估,这种情况偶尔会伴有背痛。家长的担忧通常也与外观畸形和病情的进展性有关。对于骨骼未成熟且有进展性畸形的儿童和/或青少年,支具已被证明是一种有效的非手术治疗方式。对于后凸超过70°的进展性青少年、支具治疗后仍有进展的患者、有顽固性背痛的患者以及外观畸形无法接受的患者,主张进行手术治疗。手术选择包括后路脊柱融合术,可联合或不联合通过开胸手术或电视辅助胸腔镜手术(VATS)进行的前路脊柱松解术。本文将综述青少年休曼氏胸椎后凸患者的诊断、病理生理学、体格检查结果以及非手术和手术治疗选择。

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