Yiyit Nurettin, Işıtmangil Turgut, Öksüz Sinan
Department of Thoracic Surgery, GMMA Haydarpaşa, Training Hospital, Istanbul, Turkey.
Department of Thoracic Surgery, GMMA Haydarpaşa, Training Hospital, Istanbul, Turkey.
Ann Thorac Surg. 2015 Mar;99(3):999-1004. doi: 10.1016/j.athoracsur.2014.10.036. Epub 2015 Jan 27.
Poland syndrome is a rare congenital anomaly characterized by the partial or complete absence of pectoral muscles, varying thoracic deformities, and hand anomalies. To date, many variants of this syndrome and its accompanying anomalies have been reported.
In our clinic, 113 patients were diagnosed with Poland syndrome between 1990 and 2014. A latissimus dorsi muscle transfer was performed on 6 of these patients.
Out of 113 patients, 63 (55.7%) were diagnosed with the syndrome on the right side, 42 (37.1%) were diagnosed on the left side, and 8 (7%) had a bilateral diagnosis. The partial or complete absence of the pectoralis major muscle was detected in all patients. Although 81 (71.6%) patients had a complete absence of the pectoralis major muscle, 32 (28.3%) were lacking only the sternocostal head of the muscle. In the analyzed cases, Poland syndrome was also found to be accompanied by specific anomalies. The most common anomaly accompanying Poland syndrome in these patients was Sprengel deformity, seen in 18 patients. Symmetry and stabilization of the chest wall were performed in 6 patients through transfer of the latissimus dorsi muscle.
Poland syndrome is a rare congenital anomaly, which has several variants and accompanying anomalies. The absence of several muscles in addition to the pectoral muscle can be seen in patients with Poland syndrome. Sprengel deformity is the most common accompanying anomaly. Several surgical procedures have been reported for the syndrome; for example, transposing the latissimus dorsi muscle is an effective procedure in terms of stabilizing the chest wall and providing optimum symmetric body appearance.
波兰综合征是一种罕见的先天性异常,其特征为胸肌部分或完全缺失、不同程度的胸廓畸形以及手部异常。迄今为止,该综合征的许多变体及其伴随的异常情况均有报道。
在我们诊所,1990年至2014年间有113例患者被诊断为波兰综合征。其中6例患者接受了背阔肌转移术。
113例患者中,63例(55.7%)右侧被诊断为该综合征,42例(37.1%)左侧被诊断为此病,8例(7%)为双侧诊断。所有患者均检测到胸大肌部分或完全缺失。虽然81例(71.6%)患者胸大肌完全缺失,但32例(28.3%)仅缺少胸大肌的胸肋部。在分析的病例中,还发现波兰综合征伴有特定异常。这些患者中波兰综合征最常见的伴随异常是先天性高肩胛症,见于18例患者。6例患者通过背阔肌转移术实现了胸壁的对称与稳定。
波兰综合征是一种罕见的先天性异常,有多种变体及伴随异常。波兰综合征患者除胸肌外还可见其他几块肌肉缺失。先天性高肩胛症是最常见的伴随异常。针对该综合征已报道了多种外科手术方法;例如,转移背阔肌在稳定胸壁和提供最佳对称身体外观方面是一种有效的手术方法。