Chen Dan, Zhong Wenyao, Sun Liying, Zhao Zongxuan, Tian Wen
Department of Hand Surgery, Beijing Jishuitan Hospital, Capital Medical University, 31 Xin Jie Kou Dong Jie, Xi Cheng District, Beijing, 100035, China.
BMC Musculoskelet Disord. 2025 May 13;26(1):469. doi: 10.1186/s12891-025-08719-4.
Ulnar polydactyly, a common congenital hand anomaly, exhibits significant phenotypic variability. Existing classification systems have limitations, particularly in categorizing rare variants. This study introduces a new classification system for ulnar polydactyly that addresses these limitations.
We retrospectively reviewed the medical records of 35 patients with ulnar polydactyly treated at our institution between 2010 and 2022. Data collected included patient demographics, clinical presentation, radiographic findings, family history, associated anomalies, and surgical procedures. Based on detailed morphological and radiographic assessments, we developed a novel classification system comprising five main types (0-4) and associated subtypes.
The 35 patients (23 males, 12 females) had a mean age of 3.2 years. Thirty patients had bilateral involvement, with 16 exhibiting symmetry. In total, 65 hands were affected, and one hand was excluded because the patient underwent surgery in another hospital. Type 0 was the most common (38 cases), followed by Type 4 (19 cases), Type 3 (4 cases), and Type 1 (3 cases). Our classification system effectively categorized all cases, including rare variants such as Type 1b (duplicated distal phalanx) and Type 4d (duplication originating from the deformed fourth metacarpal), which are not adequately addressed by previous classifications.
Existing classification systems for ulnar polydactyly omit two key variants: Type 1b (duplicated distal phalanx) and Type 4d (duplication from the deformed fourth metacarpal). Our system specifically incorporates these types, providing a more comprehensive framework to guide diagnosis and improve surgical planning for these rare conditions.
Retrospectively registered.
尺侧多指畸形是一种常见的先天性手部畸形,表现出显著的表型变异性。现有的分类系统存在局限性,尤其是在对罕见变异进行分类时。本研究引入了一种新的尺侧多指畸形分类系统,以解决这些局限性。
我们回顾性分析了2010年至2022年在我院接受治疗的35例尺侧多指畸形患者的病历。收集的数据包括患者人口统计学信息、临床表现、影像学检查结果、家族史、相关畸形以及手术过程。基于详细的形态学和影像学评估,我们开发了一种新的分类系统,包括五种主要类型(0 - 4型)及相关亚型。
35例患者(23例男性,12例女性)的平均年龄为3.2岁。30例患者为双侧受累,其中16例表现为对称性。总共65只手受累,1只手因患者在其他医院接受手术而被排除。0型最为常见(38例),其次是4型(19例)、3型(4例)和1型(3例)。我们的分类系统有效地对所有病例进行了分类,包括罕见变异,如1b型(远节指骨重复)和4d型(起源于畸形第四掌骨的重复),而先前的分类未能充分涵盖这些类型。
现有的尺侧多指畸形分类系统遗漏了两个关键变异:1b型(远节指骨重复)和4d型(来自畸形第四掌骨的重复)。我们的系统特别纳入了这些类型,提供了一个更全面的框架来指导诊断并改善对这些罕见病症的手术规划。
回顾性注册。