Chest wall deformities.

Acta chirurgica Hungarica Pub Date : 1999-01-01
Y Akçali, H Ceyran, L Hasdiraz
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Abstract

Background: Pectus deformities and atypical costal anomalies are congenital thoracic wall defects that can cause a marked cosmetic defect with attendant psychological trauma and limited physical performance.

Patients and methods: We reviewed 43 patients with chest wall deformities, 24 (55.8%) were pectus excavatum, 13 (30.2%) pectus carinatum and 6 (14%) atypical costal anomalies, in the last sixteen years. There were nine female and 34 (79.1%) male patients. The mean age of the patients was 14.4 years (range, 5 to 23). Scoliosis (13.5%), Poland's syndrome (5.4%), Marfan's syndrome (5.4%), neurofibromatosis (2.7%), atrial septal defect (2.7%) and mitral valve prolapse (13.5%) were associated with pectus deformities. The modified Ravitch's technique was used in pectus cases. Concomitant surgery was performed in two patients with pectus carinatum.

Results: The complications of pectus deformity repair were pneumothorax (24.3%), wound infection (8.1%), and local tissue necrosis (2.7%). There was no major recurrence, while minor recurrence rate was 10.8%. There was no mortality.

Conclusion: Timely surgical procedures for the treatment of pectus deformities result in an excellent cosmetic outcome and improve cardiorespiratory function, providing both physical and psychological benefits.

胸壁畸形。
背景:胸肌畸形和非典型肋异常是先天性胸壁缺陷,可引起明显的外观缺陷,并伴有心理创伤和身体活动受限。患者和方法:我们回顾了近16年来43例胸壁畸形患者,其中24例(55.8%)为漏斗胸,13例(30.2%)为凸胸,6例(14%)为非典型肋部异常。其中女性9例,男性34例(79.1%)。患者平均年龄为14.4岁(5 ~ 23岁)。脊柱侧凸(13.5%)、波兰综合征(5.4%)、马凡综合征(5.4%)、神经纤维瘤病(2.7%)、房间隔缺损(2.7%)和二尖瓣脱垂(13.5%)与胸肌畸形相关。改良的拉维奇技术用于胸肌病例。2例胸突患者行手术治疗。结果:胸肌畸形修复术后并发症为气胸(24.3%)、创面感染(8.1%)、局部组织坏死(2.7%)。无重大复发,轻微复发率为10.8%。没有死亡。结论:及时手术治疗胸肌畸形可获得良好的美容效果,改善心肺功能,身心均可获益。
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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