El-Naggar Ahmed, Hegazy Mohamad, Hanna Atef, Tarraf Yehia, Temtamy Samia
Department of Orthopaedics, Faculty of Medecine, Cairo University, 10, Murad St, Giza, 12511, Egypt,
J Child Orthop. 2007 Nov;1(5):313-22. doi: 10.1007/s11832-007-0057-x. Epub 2007 Oct 17.
Congenital clasped thumb is a deformity that is associated with heterogeneous congenital anomalies and it has been addressed in many congenital syndromes. The aim of this study was to diagnose and evaluate cases of clasped thumb as regards the associated congenital anomalies and syndromes, and evaluation of the results of treatment of such cases.
A prospective study on 40 patients with 73 clasped thumbs was done. All the patients' data regarding their personal, family, pregnancy and developmental histories were recorded. All the patients were exposed to thorough clinical and radiological examination and genetic assessment. The cases were classified using the Tsuyuguchi et al. (J Hand Surg [Am] 10:613-618, 1985) classification into three types. Conservative treatment was adopted in ten hands, and surgical treatment was performed for 28 hands in 17 patients, with an average follow-up of 26 months.
Positive consanguinity was recorded in 57.5% of cases. Associated anomalies were recorded in 77.5% of cases. Type I was the most common one, followed by type III and then type II. Conservative treatment is effective in type I cases when presented early, and all patients were satisfied with the results of surgical treatment.
We reported associated anomalies which are to our knowledge have not mentioned before in the literature which include; congenital blindness, radial deviation of the index finger and ventricular septal defect. We found that 68% of the patients had associated syndromes, and this has not been mentioned before. In this study, we found that there were no difference between type II and type III clasped thumb as regards the pathological findings, severity, the operative procedures, the treatment protocol and the operative results. Properly planned treatment gives satisfactory results.
先天性拇指内收畸形是一种与多种先天性异常相关的畸形,在许多先天性综合征中都有涉及。本研究的目的是诊断和评估拇指内收畸形病例的相关先天性异常和综合征,并评估此类病例的治疗结果。
对40例患者的73个拇指内收畸形进行了前瞻性研究。记录了所有患者的个人、家族、妊娠和发育史数据。所有患者均接受了全面的临床、放射学检查和基因评估。根据津口等人(《美国手外科杂志》10:613 - 618,1985年)的分类方法将病例分为三种类型。10只手采用保守治疗,17例患者的28只手进行了手术治疗,平均随访26个月。
57.5%的病例记录有近亲结婚。77.5%的病例记录有相关异常。I型最为常见,其次是III型,然后是II型。I型病例早期采用保守治疗有效,所有患者对手术治疗结果均满意。
我们报告了据我们所知在文献中未曾提及的相关异常,包括先天性失明、食指桡侧偏斜和室间隔缺损。我们发现68%的患者有相关综合征,这在之前也未曾被提及。在本研究中,我们发现II型和III型拇指内收畸形在病理表现、严重程度、手术操作、治疗方案和手术结果方面没有差异。合理规划的治疗可取得满意结果。