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本文引用的文献

1
Multidisciplinary team meetings for patients with complex extremity defects: a retrospective analysis of treatment recommendations and prognostic factors for non-implementation.多学科团队会议治疗复杂四肢缺损患者:未实施治疗建议的回顾性分析及预后因素。
BMC Surg. 2021 Mar 29;21(1):168. doi: 10.1186/s12893-021-01169-4.
2
Amniotic Constriction Bands: Secondary Deformities and Their Treatments.羊膜带综合征:继发畸形及其治疗
Hand (N Y). 2019 May;14(3):346-351. doi: 10.1177/1558944717750917. Epub 2018 Jan 10.
3
The prevalence of amnion rupture sequence, limb body wall defects and body wall defects in Alberta 1980-2012 with a review of risk factors and familial cases.1980 - 2012年阿尔伯塔省羊膜破裂序列征、肢体-体壁缺损和体壁缺损的患病率及危险因素和家族性病例回顾
Am J Med Genet A. 2017 Feb;173(2):299-308. doi: 10.1002/ajmg.a.38016. Epub 2016 Oct 14.
4
The importance of foetal movement for co-ordinated cartilage and bone development in utero : clinical consequences and potential for therapy.胎儿运动对宫内协调的软骨和骨骼发育的重要性:临床后果和治疗潜力。
Bone Joint Res. 2015 Jul;4(7):105-16. doi: 10.1302/2046-3758.47.2000387.
5
Congenital constriction band syndrome with limb defects.先天性束带综合征伴肢体缺陷。
J Pediatr Orthop. 2015 Jan;35(1):100-3. doi: 10.1097/BPO.0000000000000206.
6
Growth disturbance after distal femoral growth plate fractures in children: a meta-analysis.儿童股骨远端生长板骨折后生长障碍:一项荟萃分析。
J Orthop Trauma. 2009 Oct;23(9):663-7. doi: 10.1097/BOT.0b013e3181a4f25b.
7
Thigh-leg skin tube pedicle and amniotic band syndrome.大腿-小腿皮管蒂与羊膜带综合征
Fetal Pediatr Pathol. 2009;28(3):151-3. doi: 10.1080/15513810902772441.
8
Lumbopedal skin pedicle in an infant with the amniotic band syndrome: a Disorganization-like defect?一名患有羊膜带综合征婴儿的腰骶部皮肤蒂:类似结构紊乱的缺陷?
Clin Dysmorphol. 2003 Jan;12(1):51-4. doi: 10.1097/00019605-200301000-00009.
9
Amniotic band sequence: Streeter's hypothesis reexamined.
Am J Med Genet. 1992 Oct 1;44(3):280-7. doi: 10.1002/ajmg.1320440304.

展示并多学科管理一例独特的下肢肢体畸形病例,该病例由羊膜带综合征引起。

Presentation and multidisciplinary management of a unique case of lower limb dysmelia resulting from amniotic band syndrome.

机构信息

Burns and Plastic Surgery, Manchester University NHS Foundation Trust, Manchester, UK

Burns and Plastic Surgery, Manchester University NHS Foundation Trust, Manchester, UK.

出版信息

BMJ Case Rep. 2024 Mar 15;17(3):e258063. doi: 10.1136/bcr-2023-258063.

DOI:10.1136/bcr-2023-258063
PMID:38490707
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10946379/
Abstract

A neonate was born with a unique congenital lower limb dysmelia due to an abnormal presentation of amniotic band syndrome. An anomalous soft tissue tether from the plantar surface of the right foot to the right buttock caused extreme knee flexion, tibial rotation and malformation of the developing foot. This complex malformation required a multidisciplinary team (MDT) approach to decide between reconstruction and amputation. The band of tissue was released operatively at 73 days postdelivery, improving knee extension, and the tissue was banked on the thigh as a tube pedicle for future reconstruction. The patient underwent rehabilitation, which has been shown to be vital for synovial joint formation. At 18 months old, the decision was made to proceed with through-knee amputation and a prosthesis. The literature discussed shows the importance of an MDT approach in complex lower limb cases to give the best functional outcome for the patient.

摘要

一名新生儿因羊水带综合征的异常表现而出生时患有独特的先天性下肢畸形。从右脚足底到右臀部的异常软组织束带导致严重的膝关节屈曲、胫骨旋转和发育中足部畸形。这种复杂的畸形需要多学科团队 (MDT) 来决定是重建还是截肢。在出生后 73 天时,通过手术释放了束带组织,改善了膝关节伸展,将组织作为管状蒂存于大腿上,以备将来进行重建。患儿接受了康复治疗,这对滑膜关节形成至关重要。在 18 个月大时,决定进行膝关节下截肢和假肢安装。文献讨论表明,在复杂的下肢病例中,采用 MDT 方法对于为患者提供最佳的功能结果非常重要。