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首页> 外文期刊>Journal of plastic, reconstructive & aesthetic surgery: JPRAS >Autogenous bone graft for expansion thoracoplasty in Adam Robert Wright syndrome: a case report and review.
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Autogenous bone graft for expansion thoracoplasty in Adam Robert Wright syndrome: a case report and review.

机译:自体骨移植物治疗亚当·罗伯特·赖特综合征的胸廓扩张术:病例报告和评论。

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摘要

We present a direct anterior sternal split expansion as a surgical option for a case of severe Thoracic Insufficiency Syndrome (TIS) in an arthrogryposis-like patient. This patient's clinical features were published as a newly described syndrome: Adam Robert Wright Syndrome. The patient born with this syndrome displays characteristic craniofacial abnormalities, severe thoracic insufficiency syndrome, cleft palate, limb contractures, arthrogryposis, pulmonary hypoplasia, cryptorchidism, ophthalmoplegia and retinopathy, with normal intelligence. His severe thoracic insufficiency necessitated an urgent life-saving surgical intervention for a progressively worsening sleep apnoea and respiratory distress. We present a review of published data of sternal expansion thoracoplasty from 1965 to 2007 found in the literature. We demonstrate that direct anterior sternal split thoracoplasty with autogenous rib grafts is an effective technique for the acute management of thoracic insufficiency syndrome in this specific case. This procedure provided our patient with symptomatic benefit. To our knowledge, this is the only reported surgical management of thoracic insufficiency syndrome demonstrating a statistical improvement in chest wall compliance and tidal volume. We show that direct anterior sternal split expansion is a surgical treatment option in some patients with thoracic insufficiency syndrome. Our surgical strategy for the management of severe thoracic insufficiency syndrome in Adam Robert Wright Syndrome provided symptomatic relief and favourable long-term results.
机译:我们提出了一种直接的胸骨前裂扩张术,作为关节置换术样患者中严重胸功能不全综合征(TIS)的手术选择。该患者的临床特征已被公布为一种新描述的综合征:亚当·罗伯特·赖特综合征。患有该综合征的患者表现出典型的颅面畸形,严重的胸功能不全综合征,left裂,肢体挛缩,关节置换,肺发育不全,隐睾,眼肌麻痹和视网膜病变,智力正常。他严重的胸椎功能不全,需要紧急进行挽救生命的外科手术,以使睡眠呼吸暂停和呼吸窘迫逐渐加重。我们对文献中发现的自1965年至2007年的胸骨扩张胸廓成形术的已发表数据进行综述。我们证明,自体肋骨移植术直接进行胸骨前胸裂成形术是在这种特殊情况下对胸功能不全综合征进行急性治疗的有效技术。该程序为我们的患者提供了对症治疗。据我们所知,这是唯一报告的胸功能不全综合征的外科手术治疗,显示出胸壁顺应性和潮气量的统计学改善。我们表明,在某些胸廓功能不全综合征患者中,胸骨前裂直接扩展是一种手术治疗选择。我们针对亚当·罗伯特·赖特综合征的严重胸功能不全综合征的治疗策略可缓解症状并取得长期良好效果。

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