Pandey Abhishek, Kayastha Sabik R, Pande Prasamsa, Silwal Prabhat, Upadhyaya Prashant, Pandey Archana, Keshari Suraj, Dhungana Sanjay, Singh Yadvinder
Dhulikhel Hospital, Kavre, Bagmati, Nepal.
Department of Orthopedics & Traumatology, Kathmandu University School of Medical Sciences, Kavre, Bagmati, Nepal.
Ann Med Surg (Lond). 2025 Jan 9;87(1):43-48. doi: 10.1097/MS9.0000000000002763. eCollection 2025 Jan.
Sprengel deformity (SD) is a rare congenital deformity consisting of elevation of the scapula, leading to limited range of motion and a visible lump in severe cases. Klippel-Feil syndrome is a rare congenital abnormality characterized by the triad of cervical synostosis, low posterior hairline, and short neck. It is often associated with SD.
We present two cases of SD of a 7-year-old boy and a 10-year-old boy. They were both born with the abnormality and complained of limited range of motion in the affected shoulder.
Patients with less severe forms of SD can lead a normal life with supportive treatment, and it is not connected with cognitive impairment; however, there may be a limited range of motion and cosmetic concerns. In severe cases, treatment entails operative therapy with corrective placement of the scapula and resection of the omovertebral band.
Patients with SD require supportive physiotherapy from a young age. Severe cases need operative treatment at a young age. The modified Woodward approach may be an excellent surgical option to correct the deformity.
先天性高肩胛症(SD)是一种罕见的先天性畸形,表现为肩胛骨抬高,严重时会导致活动范围受限并出现明显肿块。克利珀尔-费尔综合征是一种罕见的先天性异常,其特征为颈椎融合、后发际线低和颈部短三联征。它常与先天性高肩胛症相关。
我们报告了一名7岁男孩和一名10岁男孩患先天性高肩胛症的两个病例。他们均出生时即患有该异常,且均主诉患侧肩部活动范围受限。
症状较轻的先天性高肩胛症患者通过支持性治疗可正常生活,且与认知障碍无关;然而,可能存在活动范围受限和外观问题。在严重病例中,治疗需要进行手术治疗,包括肩胛骨的矫正复位和肩胛背神经切断术。
先天性高肩胛症患者自幼即需要支持性物理治疗。严重病例需要在幼年时进行手术治疗。改良的伍德沃德手术方法可能是矫正该畸形的一种极佳手术选择。