Das B K, Matin A, Hassan G Z, Hossain M Z, Zaman M A
Department of Pediatric Surgery, ZH Sikder Women's Medical College, Dhaka, Bangladesh.
Mymensingh Med J. 2010 Oct;19(4):555-60.
Congenital Muscular Torticollis (CMT) is a postural deformity of head and neck detected at birth or shortly after birth, primarily resulting from unilateral shortening of Sternocleidomastoid Muscle (SCM). In neonates and infants, patient may cure conservatively by physiotherapy but surgery is the treatment of choice for children and adolescents. There are various techniques of surgery. Here we show our experience regarding management of congenital muscular torticollis. In the present retrospective case series, fourteen patients of congenital muscular torticollis were treated. The cases were enrolled between Nov' 2005 to Oct' 2007 in Bangabandhu Sheikh Mujib Medical University, Gonosasthaya Somaj Vittik Medical College Hospital, Dhaka and different private clinics of Dhaka city of Bangladesh. Neonates and infants were treated conservatively with physiotherapy and others treated surgically by transection of both sternal and clavicular head of SCM under general anesthesia. Operated patients were released on following post operative day with advised to do physiotherapy. Patients age range from 7 days to 15 years of which ten were female and four male. SCM was shortened in all cases (8 on right side and 6 on left side). Eleven were female and three male. Of 14 patients, 2 neonates, 7 infants and 5 were more than 1 year age. There was no associated anomaly. Out of 9 neonates and infants 8 cured conservatively with physiotherapy and another one significantly improved. Six were treated surgically including one failed physiotherapy. Post operative period was uneventful and there was no complication. Results were evaluated clinically and comments of peers. Most of the patient of congenital muscular torticollis can be treated conservatively during infancy. Division of both sternal and clavicular head of SCM is easy and safe surgical technique for the treatment of CMT of older children and adolescents.
先天性肌性斜颈(CMT)是一种在出生时或出生后不久被发现的头颈部姿势畸形,主要由胸锁乳突肌(SCM)单侧缩短引起。在新生儿和婴儿中,患者可通过物理治疗保守治愈,但手术是儿童和青少年的首选治疗方法。手术有多种技术。在此我们展示我们关于先天性肌性斜颈治疗的经验。在本回顾性病例系列中,对14例先天性肌性斜颈患者进行了治疗。这些病例于2005年11月至2007年10月在孟加拉国达卡的班加班杜·谢赫·穆吉布医科大学、戈诺萨斯塔亚·索马吉·维蒂克医学院医院以及达卡市的不同私人诊所登记入组。新生儿和婴儿采用物理治疗进行保守治疗,其他患者在全身麻醉下通过横断胸锁乳突肌的胸骨和锁骨头部进行手术治疗。手术患者在术后次日出院,并建议进行物理治疗。患者年龄范围从7天至15岁,其中10例为女性,4例为男性。所有病例中胸锁乳突肌均缩短(右侧8例,左侧6例)。11例为女性,3例为男性。14例患者中,2例为新生儿,7例为婴儿,5例年龄超过1岁。无相关异常。9例新生儿和婴儿中,8例通过物理治疗保守治愈,另一例明显改善。6例接受手术治疗,其中1例物理治疗失败。术后过程顺利,无并发症。通过临床评估结果并征求同行意见。大多数先天性肌性斜颈患者在婴儿期可保守治疗。横断胸锁乳突肌的胸骨和锁骨头部是治疗大龄儿童和青少年先天性肌性斜颈的一种简单且安全的手术技术。