Płomiński Janusz, Olesińska Jolanta, Kamelska-Sadowska Anna Malwina, Nowakowski Jacek Józef, Zaborowska-Sapeta Katarzyna
Prof. Adam Gruca Independent Public Clinical Hospital CMKP, 05-400 Otwock, Poland.
Centre of Postgraduate Medical Education, 01-813 Warsaw, Poland.
Healthcare (Basel). 2023 Dec 20;12(1):13. doi: 10.3390/healthcare12010013.
Congenital muscular torticollis (CMT) is an asymmetrical head position resulting from structural changes in the sternocleidomastoid (SCM) muscle that occurs early during a child's development or due to perinatal trauma. Children with CMT exhibit a marked imbalance in tension between the SCMs. In a typical clinical picture, an ultrasound scan is performed to reveal characteristic lesions, such as tissue fibrosis or post-traumatic changes. An early diagnosis of CMT in newborns and the implementation of treatment offer the chance of a complete resolution. Torticollis treatment aims to restore the SCM's normal function. Surgical treatment is performed when conservative methods fail to improve the patient's condition. The indications that surgery is needed include a marked shortening of the SCM, persistent fibrosis in the muscle, constant head and facial asymmetry, and rotation or lateral flexion in the cervical spine restricted by >15°. Of all the newborn and infant anomalies, congenital torticollis is the third most common after hip dysplasia and equinovarus deformities. Some authors demonstrate that torticollis coexists with hip dysplasia.
The aim of this study was to collect data on infants referred to paediatric rehabilitation and to identify the risk factors associated with CMT in this group of patients, as well as to assess demographic and clinical characteristics concerning risk factors.
The target population for this retrospective study consisted of 111 infants aged 0 to 5 months born in Poland and diagnosed with and undergoing treatment due to CMT. The following were determined: the relationship between the side of the CMT location and the type of delivery (caesarean section vs. vaginal), the relationship between the body weight at birth and the side of the CMT location, the relationship between the extent of SCM thickening and the type of delivery, and the incidence of CMT depending on the order of delivery.
The data revealed that CMT is less common in female infants ( = 51, 46%) compared to male ( = 61, 54%) infants, in whom a greater birth weight was reported ( < 005). Seventy-six percent (76%) of the paediatric patients with CMT were the offspring of primipara mothers. More often, children born via vaginal delivery had left-sided torticollis with a more significant broadening of the SCM, as shown on ultrasound scans, than right-sided torticollis. Theories of torticollis development pathophysiology should be deepened and systematised, and further research is needed.
先天性肌性斜颈(CMT)是一种不对称的头部姿势,由胸锁乳突肌(SCM)结构变化引起,这种变化发生在儿童发育早期或由于围产期创伤。患有CMT的儿童在双侧胸锁乳突肌之间表现出明显的张力失衡。在典型的临床症状中,会进行超声扫描以发现特征性病变,如组织纤维化或创伤后改变。新生儿期对CMT进行早期诊断并实施治疗,有机会实现完全康复。斜颈治疗旨在恢复胸锁乳突肌的正常功能。当保守方法无法改善患者病情时,则进行手术治疗。需要手术的指征包括胸锁乳突肌明显缩短、肌肉持续纤维化、头部和面部持续不对称以及颈椎旋转或侧屈受限超过15°。在所有新生儿和婴儿畸形中,先天性斜颈是继髋关节发育不良和马蹄内翻足畸形之后第三常见的疾病。一些作者表明斜颈与髋关节发育不良共存。
本研究的目的是收集转诊至儿科康复的婴儿的数据,确定该组患者中与先天性肌性斜颈相关的危险因素,并评估与危险因素相关的人口统计学和临床特征。
这项回顾性研究的目标人群为111名0至5个月大的波兰婴儿,他们被诊断患有先天性肌性斜颈并正在接受治疗。确定了以下内容:先天性肌性斜颈位置侧与分娩方式(剖宫产与阴道分娩)之间的关系、出生体重与先天性肌性斜颈位置侧之间的关系、胸锁乳突肌增厚程度与分娩方式之间的关系以及根据分娩顺序的先天性肌性斜颈发病率。
数据显示先天性肌性斜颈在女婴(n = 51,46%)中比男婴(n = 61,54%)中更少见,男婴出生体重更高(P < 0.05)。7六岁的先天性肌性斜颈儿科患者是初产妇母亲的后代。经阴道分娩的儿童中,左侧斜颈且超声扫描显示胸锁乳突肌增宽更明显的情况比右侧斜颈更常见。斜颈发育病理生理学理论应进一步深化和系统化,还需要进一步研究。