Afolabi Oluwatosin Gabriel, Adeyemi Ademola Samuel, Aitalokhai Imiekame Mimi
Department of Orthopaedic Surgery, Federal Teaching Hospital Ido-Ekiti Ekiti State,Nigeria.
Department of Nursing, Federal Teaching Hospital Ido-Ekiti Ekiti State, Nigeria.
J Orthop Case Rep. 2025 Apr;15(4):171-175. doi: 10.13107/jocr.2025.v15.i04.5488.
Radial aplasia is a rare congenital anomaly of the upper limbs, more common in females, affecting between one in 30,000 and one in 100,000 live births, and primarily impacting structures on the radial side of the forearm. While there have been numerous articles on bilateral radial aplasia and its management, this case is particularly significant as it represents the index case for our hospital. It is the first report to highlight how limited resources can lead to unfavorable outcomes in the management of this condition. In addition, it aims to stimulate the interest of the global orthopedics community to develop interventions or modify current treatment options that can be successfully implemented in low-resource settings to improve outcomes, especially the functionality of the limbs. By documenting this case, we aim to shed light on the challenges faced in resource-limited settings and advocate for increased investment in training pediatric orthopedic specialist to enhance the quality of life for affected children.
A 1-year-old boy of African descent presented with bilateral radial club hand. The patient exhibited characteristics of classical radial club hand, with complete absence of the radius and thumbs bilaterally, resulting in the nonexistence of the radio-carpal and radio-ulna joints. The forearm and ulna were shorter, with the ulna's diaphysis curved toward the radius. No hematological abnormalities were noted, and the case was non-syndromic with no identifiable risk factors. The patient underwent serial manipulation and casting for 17 months to achieve sufficient soft tissue stretching and passive correction of the deformity before the centralization procedure.
This case underscores the urgent need for improved access to specialized pediatric orthopedic care, advanced intraoperative imaging tools, and comprehensive, continuous parent education on realistic treatment expectations for patients with bilateral radial club hand. Addressing these limitations can enhance long-term outcomes and quality of life for children with this condition. This case report is of particular interest to both current and intending pediatric orthopedic specialists and highlights the broader clinical impact of resource limitations on treatment outcomes. In addition, it significantly advances our knowledge of the challenges faced in managing severe congenital anomalies in resource-limited settings.
桡骨发育不全是一种罕见的上肢先天性畸形,在女性中更为常见,在每30000至100000例活产中约有1例受影响,主要影响前臂桡侧的结构。虽然已有许多关于双侧桡骨发育不全及其治疗的文章,但本病例尤为重要,因为它是我院的首例病例。这是第一份强调资源有限如何导致这种疾病治疗结果不佳的报告。此外,它旨在激发全球骨科界的兴趣,以开发可在资源有限环境中成功实施的干预措施或改进现有治疗方案,以改善治疗结果,特别是肢体功能。通过记录本病例,我们旨在阐明资源有限环境中面临的挑战,并倡导增加对儿科骨科专家培训的投入,以提高受影响儿童的生活质量。
一名1岁非洲裔男孩患有双侧桡侧多指畸形。该患者表现出典型桡侧多指畸形的特征,双侧桡骨和拇指完全缺失,导致桡腕关节和桡尺关节不存在。前臂和尺骨较短,尺骨干向桡骨弯曲。未发现血液学异常,该病例为非综合征性,无明确危险因素。在进行中心化手术前,患者接受了17个月的连续手法复位和石膏固定,以实现足够的软组织拉伸和畸形的被动矫正。
本病例强调了迫切需要改善获得专业儿科骨科护理、先进的术中成像工具以及对双侧桡侧多指畸形患者的家长进行全面、持续的关于现实治疗期望的教育。解决这些限制可以提高这种疾病患儿的长期治疗效果和生活质量。本病例报告对于现任和未来的儿科骨科专家都特别有意义,并突出了资源限制对治疗结果的更广泛临床影响。此外,它显著推进了我们对资源有限环境中管理严重先天性畸形所面临挑战的认识。