Seeor Lisa-Marie, Fujak Albert, Dussa Chakravarthy U
Department of Trauma and Orthopaedic Surgery, Pediatric and Neuro Orthopaedics, University Hospital Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Krankenhausstr. 12, 91054 Erlangen, Bavaria Germany.
Paediatric and Neuro-Orthopaedics, Department of Orthopaedics and Traumatology, Ludwig-Maximillian-Universität, Klinikum Großhadern, Marchioninistrasse 15, 81377 Munich, Bavaria Germany.
Indian J Orthop. 2025 Mar 21;59(5):650-658. doi: 10.1007/s43465-025-01359-9. eCollection 2025 May.
Tibial hemimelia is a rare malformation with a wide clinical spectrum of presentation. The severity of this condition can be typed using different classification systems. It can exist as an independent entity or can be associated with upper limb or visceral malformations. The aims of our study are therefore, a. to report the incidence of upper limb deformities in relation to the severity of tibial hemimelia classified by the Jones classification, b. incidence of tibial hemimelia as a part of a syndrome c. to report the overall incidence of the associated upper limb and visceral deformities.
A retrospective study was done using radiographs and clinical notes. The severity of the tibia deformity was assessed using the Jones classification. The clinical notes were reviewed to report the additional findings in the upper limbs and the visceral organs.
The study included 69 patients with tibial hemimelia aged from 10 months to 34 years. Twenty of them (28.9%) had bilateral involvement. Additional malformations were observed in 56 patients (81%) involving the upper and lower limb and visceral organs. In 11 patients (16%), tibial hemimelia occurred as part of a syndrome, most often being Gollop-Wolfgang complex. The incidence of malformations of the upper extremities was 15 (21.7%), four of which (26.6%) involved bilateral upper extremity malformation. The cleft hand was the most frequent malformation of the upper extremities, followed by hypoplasia or aplasia of the thumb and fingers.
Jones type I tibial hemimelia is often associated with visceral and upper limb malformations. visceral anomalies are associated with syndromal forms of Tibiail hemimelia. Several forms of upper limb malformations with varying severity were associated with the disorder. Therefore, a holistic approach to the patient should be initiated soon after birth involving a paediatric, hand and visceral surgeon, to provide the best possible care.
Level IV study, retrospective review of 69 patients with tibial hemimelia.
胫骨半肢畸形是一种罕见的畸形,临床表现范围广泛。这种疾病的严重程度可以使用不同的分类系统进行分型。它可以作为一个独立的实体存在,也可以与上肢或内脏畸形相关联。因此,我们研究的目的是:a. 报告根据琼斯分类法分类的胫骨半肢畸形严重程度与上肢畸形的发生率;b. 胫骨半肢畸形作为综合征一部分的发生率;c. 报告相关上肢和内脏畸形的总体发生率。
使用X线片和临床记录进行回顾性研究。采用琼斯分类法评估胫骨畸形的严重程度。查阅临床记录以报告上肢和内脏器官的其他发现。
该研究纳入了69例年龄在10个月至34岁之间的胫骨半肢畸形患者。其中20例(28.9%)为双侧受累。56例(81%)患者观察到其他畸形,累及上肢、下肢和内脏器官。11例(16%)患者的胫骨半肢畸形是综合征的一部分,最常见的是戈洛普 - 沃尔夫冈复合体。上肢畸形的发生率为15例(21.7%),其中4例(26.6%)为双侧上肢畸形。裂手是上肢最常见的畸形,其次是拇指和手指发育不全或缺失。
琼斯I型胫骨半肢畸形常与内脏和上肢畸形相关。内脏异常与胫骨半肢畸形的综合征形式相关。几种不同严重程度的上肢畸形与该疾病相关。因此,出生后应尽快由儿科、手外科和内脏外科医生对患者采取整体治疗方法,以提供尽可能好的护理。
IV级研究,对69例胫骨半肢畸形患者的回顾性分析。