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波兰综合征胸廓畸形的外科治疗。

Surgical treatment of thoracic deformity in Poland's syndrome.

作者信息

Shamberger R C, Welch K J, Upton J

机构信息

Department of Surgery, Children's Hospital, Harvard Medical School, Boston, MA.

出版信息

J Pediatr Surg. 1989 Aug;24(8):760-5; discussion 766. doi: 10.1016/s0022-3468(89)80532-9.

Abstract

In 1841, Poland described congenital deficiency of the pectoralis major and minor muscles associated with syndactyly. This syndrome is a spectrum, often involving chest wall and breast deformity as well. Identification of the various musculoskeletal components involved permits optimal thoracic reconstruction in the small proportion of patients who will require it. From 1955 to 1988, 75 patients (40 males and 35 females) with Poland's syndrome were treated or evaluated. Patients with isolated deficiencies of the pectoral muscles, breast, or hand deformity were excluded. The complex was right-sided in 44 patients, left-sided in 30, and bilateral in one. The pectoralis minor and the costal portion of the pectoralis major muscle were absent in all patients. Hand anomalies were present in 50 patients. Athelia and/or amastia were noted in 37 patients. In ten patients, the rib cage deformity required reconstruction, and in three cases, rib or cartilage grafts were needed for complete repair. Often unappreciated in these cases is the significant rotation of the sternum toward the involved side and contralateral carinate deformity. Correction is achieved by bilateral subperichondrial costal cartilage resection and sternal osteotomy (seven of ten patients), thus allowing anterior displacement and orthorotation of the sternum. Chest wall reconstruction must be tailored to the requirements of each patient. No intraoperative or postoperative complications occurred in these ten patients. In males without rib cage deformity, generally no treatment is required to replace the absent pectoral muscles, although in two cases rotation of the latissimus dorsi muscle was performed. In all females, reconstruction of the ipsilateral breast is required at full development.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

1841年,波兰描述了伴有并指畸形的胸大肌和胸小肌先天性缺损。该综合征表现多样,常累及胸壁和乳房畸形。明确所涉及的各种肌肉骨骼成分,有助于为少数有需求的患者进行最佳的胸廓重建。1955年至1988年,对75例波兰综合征患者(40例男性和35例女性)进行了治疗或评估。排除了单纯胸肌、乳房缺损或手部畸形的患者。该综合征复合体右侧44例,左侧3例,双侧1例。所有患者均无胸小肌及胸大肌的肋骨部分。50例患者存在手部异常。37例患者有乳头缺如和/或乳房缺如。10例患者的胸廓畸形需要重建,3例患者需要肋骨或软骨移植来完成修复。这些病例中常被忽视的是胸骨向患侧的明显旋转及对侧嵴突畸形。通过双侧软骨膜下肋软骨切除和胸骨截骨术(10例患者中的7例)进行矫正,从而使胸骨向前移位并矫正旋转。胸廓重建必须根据每位患者的需求进行定制。这10例患者术中及术后均未发生并发症。对于无胸廓畸形的男性,一般无需治疗来替代缺失的胸肌,不过有2例患者进行了背阔肌转位术。所有女性患者在乳房完全发育时均需要进行同侧乳房重建。(摘要截选至250词)

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