Soultanis Konstantinos C, Payatakes Alexandros H, Chouliaras Vasilios T, Mandellos Georgios C, Pyrovolou Nikolaos E, Pliarchopoulou Fani M, Soucacos Panayotis N
1st Department of Orthopaedic Surgery, School of Medicine, University of Athens, "Attikon" Hospital, Rimini 1 Haidari 12462, Athens, Greece.
Scoliosis. 2007 Oct 23;2:15. doi: 10.1186/1748-7161-2-15.
Spine deformity can be idiopathic (more than 80% of cases), neuromuscular, congenital or neurofibromatosis-related. However, there are many disorders that may also be involved. We present our experience treating patients with scoliosis or other spine deformities related to rare clinical entities.
A retrospective study of the records of a school-screening study in North-West Greece was performed, covering a 10-year period (1992-2002). The records were searched for patients with deformities related to rare disorders. These patients were reviewed as regards to characteristics of underlying disorder and spine deformity, treatment and results, complications, intraoperative and anaesthesiologic difficulties particular to each case.
In 13 cases, the spine deformity presented in relation to rare disorders. The underlying disorder was rare neurological disease in 2 cases (Rett syndrome, progressive hemidystonia), muscular disorders (facioscapulohumeral muscular dystrophy, arthrogryposis) in 2 patients, osteogenesis imperfecta in 2 cases, Marfan syndrome, osteopetrosis tarda, spondyloepiphyseal dysplasia congenita, cleidocranial dysplasia and Noonan syndrome in 1 case each. In 2 cases scoliosis was related to other congenital anomalies (phocomelia, blindness). Nine of these patients were surgically treated. Surgery was avoided in 3 patients.
This study illustrates the fact that different disorders are related with curves with different characteristics, different accompanying problems and possible complications. Investigation and understanding of the underlying pathology is an essential part of the clinical evaluation and preoperative work-up, as clinical experience at any specific center is limited.
脊柱畸形可能是特发性的(超过80%的病例)、神经肌肉性的、先天性的或与神经纤维瘤病相关的。然而,也可能涉及许多其他疾病。我们介绍了我们治疗与罕见临床实体相关的脊柱侧弯或其他脊柱畸形患者的经验。
对希腊西北部一项为期10年(1992 - 2002年)的学校筛查研究记录进行回顾性研究。在记录中查找与罕见疾病相关的畸形患者。对这些患者的基础疾病特征、脊柱畸形情况、治疗及结果、并发症、每个病例特有的术中及麻醉困难进行了评估。
13例患者的脊柱畸形与罕见疾病相关。基础疾病为罕见神经疾病的有2例(雷特综合征、进行性偏侧肌张力障碍),肌肉疾病(面肩肱型肌营养不良、关节挛缩症)的有2例,成骨不全的有2例,马凡综合征、迟发性骨硬化、先天性脊椎骨骺发育不良、锁骨颅骨发育不全和努南综合征各1例。2例脊柱侧弯与其他先天性异常(短肢畸形、失明)有关。其中9例患者接受了手术治疗。3例患者未进行手术。
本研究表明,不同疾病与具有不同特征、不同伴随问题及可能并发症的脊柱侧弯相关。对基础病理的研究和理解是临床评估及术前检查的重要组成部分,因为任何特定中心的临床经验都是有限的。