胫骨偏瘫上肢畸形的发生:与琼斯分类的相关性。

IF 1.1 4区 医学 Q3 ORTHOPEDICS
Indian Journal of Orthopaedics Pub Date : 2025-03-21 eCollection Date: 2025-05-01 DOI:10.1007/s43465-025-01359-9
Lisa-Marie Seeor, Albert Fujak, Chakravarthy U Dussa
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引用次数: 0

摘要

背景:胫骨偏瘫是一种罕见的畸形,临床表现广泛。这种情况的严重程度可以使用不同的分类系统进行分类。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有关。因此,我们研究的目的是:a.报告上肢畸形的发生率与Jones分类法分类的胫骨偏瘫严重程度的关系;b.胫骨偏瘫作为综合征的一部分的发生率;c.报告相关上肢和内脏畸形的总体发生率。方法:利用x线片和临床记录进行回顾性研究。胫骨畸形的严重程度采用琼斯分级法进行评估。我们回顾了临床记录,报告了上肢和内脏器官的其他发现。结果:本研究纳入69例胫骨偏瘫患者,年龄10个月~ 34岁。其中20例(28.9%)双侧受累。56例(81%)患者出现了累及上肢、下肢和内脏器官的畸形。在11例(16%)患者中,胫骨偏瘫作为综合征的一部分发生,最常见的是Gollop-Wolfgang复合体。上肢畸形15例(21.7%),其中双侧上肢畸形4例(26.6%)。上肢最常见的畸形是手裂,其次是拇指和手指发育不全或发育不全。结论:琼斯型胫骨偏瘫常伴有内脏和上肢畸形。内脏异常与胫骨偏瘫综合征有关。几种不同严重程度的上肢畸形与这种疾病有关。因此,应该在出生后不久就开始对患者进行全面的治疗,包括儿科、手部和内脏外科医生,以提供最好的护理。证据水平:IV级研究,回顾性分析69例胫骨偏瘫患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Occurrence of Malformations of the Upper Extremity in Tibial Hemimelia: Correlation with the Jones Classification.

Background: 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.

Methods: 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.

Results: 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.

Conclusion: 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 of evidence: Level IV study, retrospective review of 69 patients with tibial hemimelia.

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来源期刊
CiteScore
1.80
自引率
0.00%
发文量
185
审稿时长
9 months
期刊介绍: IJO welcomes articles that contribute to Orthopaedic knowledge from India and overseas. We publish articles dealing with clinical orthopaedics and basic research in orthopaedic surgery. Articles are accepted only for exclusive publication in the Indian Journal of Orthopaedics. Previously published articles, articles which are in peer-reviewed electronic publications in other journals, are not accepted by the Journal. Published articles and illustrations become the property of the Journal. The copyright remains with the journal. Studies must be carried out in accordance with World Medical Association Declaration of Helsinki.
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