Fülling Tim, Baade Carsten, Dragu Adrian, Nicklas Antek
Abteilung für Plastische und Handchirurgie UniversitätsCentrum für Orthopädie, Unfall- & Plastische Chirurgie, Universitätsklinikum Carl Gustav Carus an der Technischen Universität Dresden, Dresden, Germany.
Helios Weißeritztal-Kliniken GmbH, Freital, Germany.
Arch Orthop Trauma Surg. 2025 Jan 3;145(1):107. doi: 10.1007/s00402-024-05724-5.
Kirner deformity is a rare anomaly of the little finger in adolescents, characterized by a deformity of the distal phalanx and a radiologically L-shaped epiphysis, along with palmar and radial angulation of the distal phalanx. Due to the rarity of these pathological findings, there are no systematic literature reviews available. This work serves as an overview of the clinical presentation, frequency and age distributions, as well as possible conservative and surgical treatment options.
We present five cases of patients with Kirner's deformity of the little finger who underwent surgical treatment. A partial tenotomy of the flexor digitorum profundus tendon from the metaphyseal/diaphyseal distal phalanx was performed. In one case, a dorsal epiphysiodesis was also carried out. Additionally, a systematic review of the literature on Kirner's deformity was conducted, summarizing the prevalence, previously used surgical treatment options, and epidemiological data.
In the presented cases, the detachment of the FDP tendon and dorsal epiphysiodesis resulted in a good functional and aesthetic outcome. Regarding the epidemiological distribution of Kirner deformity, it is noted that significantly more females are affected than males (63% vs. 36%). The average age at presentation in the respective clinic was 9.36 years (± 2.5). In more than half of all reported cases, the deformity was bilateral. Surgical intervention was performed in only 7.4% of cases, which included FDP detachment or corrective osteotomies. More than 90% of patients were treated conservatively.
Kirner's deformity is a rare condition affecting adolescents. In cases where functional limitations or pain symptoms are present, we recommend surgical intervention via detachment of the FDP tendon. If the deformity is an incidental finding without functional or aesthetic limitations, conservative therapy with a corrective splint can be initiated. From our perspective, early surgical treatment before the age of 12 improves both the long-term functional and aesthetic outcomes.
基尔纳畸形是青少年小指的一种罕见异常,其特征为远节指骨畸形、放射学上呈L形骨骺,以及远节指骨掌侧和桡侧成角。由于这些病理表现罕见,目前尚无系统性的文献综述。本研究旨在概述其临床表现、发病率及年龄分布,以及可能的保守和手术治疗方案。
我们报告了5例接受手术治疗的小指基尔纳畸形患者。对远节指骨干骺端/骨干处的指深屈肌腱进行部分切断术。其中1例还进行了背侧骨骺阻滞术。此外,对基尔纳畸形的文献进行了系统综述,总结了患病率、既往使用的手术治疗方案及流行病学数据。
在本研究病例中,指深屈肌腱切断术和背侧骨骺阻滞术取得了良好的功能和美学效果。关于基尔纳畸形的流行病学分布,发现女性受累明显多于男性(63%对36%)。各诊所患者的平均就诊年龄为9.36岁(±2.5)。在所有报告病例中,超过一半的畸形为双侧性。仅7.4%的病例进行了手术干预,包括指深屈肌腱切断术或矫正截骨术。超过90%的患者接受了保守治疗。
基尔纳畸形是一种影响青少年的罕见疾病。对于存在功能受限或疼痛症状的病例,我们建议通过指深屈肌腱切断术进行手术干预。如果畸形是偶然发现且无功能或美学限制,可开始使用矫正夹板进行保守治疗。我们认为,12岁前进行早期手术治疗可改善长期功能和美学效果。