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本文引用的文献

1
Progressive overgrowth of the cerebriform connective tissue nevus in patients with Proteus syndrome.脑叶型脑连接组织痣在Proteus 综合征患者中的进行性过度生长。
J Am Acad Dermatol. 2010 Nov;63(5):799-804. doi: 10.1016/j.jaad.2009.12.012. Epub 2010 Aug 14.
2
Proteus syndrome: a case report.变形综合征:一例报告
Am Surg. 2009 Sep;75(9):853-6.
3
Pain in adults with cerebral palsy: impact and solutions.成人脑瘫患者的疼痛:影响与解决方案。
Dev Med Child Neurol. 2009 Oct;51 Suppl 4:113-21. doi: 10.1111/j.1469-8749.2009.03423.x.
4
Proteus syndrome complicated by multiple spinal meningiomas.变形综合征合并多发脊髓脑膜瘤。
Clin Exp Dermatol. 2008 Nov;33(6):729-32. doi: 10.1111/j.1365-2230.2008.02846.x. Epub 2008 Aug 2.
5
Newly delineated syndrome of congenital lipomatous overgrowth, vascular malformations, and epidermal nevi (CLOVE syndrome) in seven patients.7例患者中发现的先天性脂肪瘤过度生长、血管畸形和表皮痣(CLOVE综合征)新界定综合征。
Am J Med Genet A. 2007 Dec 15;143A(24):2944-58. doi: 10.1002/ajmg.a.32023.
6
Parenting children with Proteus syndrome: experiences with, and adaptation to, courtesy stigma.养育患有变形综合征的孩子:应对并适应附带污名的经历。
Am J Med Genet A. 2007 Sep 15;143A(18):2089-97. doi: 10.1002/ajmg.a.31904.
7
Type 2 segmental Cowden disease vs. Proteus syndrome.
Br J Dermatol. 2007 May;156(5):1089-90. doi: 10.1111/j.1365-2133.2007.07818.x. Epub 2007 Mar 28.
8
The challenges of Proteus syndrome: diagnosis and management.变形综合征的挑战:诊断与管理
Eur J Hum Genet. 2006 Nov;14(11):1151-7. doi: 10.1038/sj.ejhg.5201638. Epub 2006 Aug 2.
9
Bisphosphonate treatment of bone fibrous dysplasia in McCune-Albright syndrome.
J Pediatr Endocrinol Metab. 2006 May;19 Suppl 2:583-93. doi: 10.1515/jpem.2006.19.s2.583.
10
Sudden death caused by pulmonary thromboembolism in Proteus syndrome.变形综合征中由肺血栓栓塞引起的猝死。
Clin Genet. 2000 Nov;58(5):386-9. doi: 10.1034/j.1399-0004.2000.580509.x.

变形综合征的骨科及其他并发症的评估与管理

Assessment and management of the orthopedic and other complications of Proteus syndrome.

作者信息

Tosi Laura L, Sapp Julie C, Allen Elizabeth S, O'Keefe Regis J, Biesecker Leslie G

机构信息

Division of Orthopaedic Surgery and Sports Medicine, Children's National Medical Center, 111 Michigan Avenue, NW, Washington, DC 20010 USA ; Genetic Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD USA.

出版信息

J Child Orthop. 2011 Oct;5(5):319-27. doi: 10.1007/s11832-011-0350-6. Epub 2011 May 28.

DOI:10.1007/s11832-011-0350-6
PMID:23024722
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3179535/
Abstract

PURPOSE

A multidisciplinary workshop was convened at the National Institutes of Health (NIH) to discuss the management of the orthopedic and other complications of Proteus syndrome (PS), a progressive, disproportionate overgrowth disorder. While PS poses many complex challenges, the focus of the workshop was the management of the asymmetric and disorganized skeletal overgrowth that characterizes this multisystem disorder.

METHODS

Workshop participants developed recommendations for clinical research and patient management and surveillance to maximize the benefits and reduce the risks of surgical and other interventions.

RESULTS

Recommendations for clinical care and management included assessments of skeletal overgrowth and its progression with modalities such as X-ray, magnetic resonance imaging (MRI), dual-energy X-ray absorptiometry, and computerized tomography (CT) imaging. The recommendations also cover the assessment of non-orthopedic complications of PS that significantly impact surgical risk, such as pulmonary embolism and lung bullae. Surgical considerations in PS include assessment of the contribution of contractures to deformities and prophylactic soft-tissue release, aggressive and early use of epiphysiodesis and epiphysiostasis, amputation, and spinal bracing.

CONCLUSION

Decisions on the timing of orthopedic procedures in children with PS are challenging because they entail balancing the risks of intervention in this high-risk and complex population against the increasing morbidity that patients experience with progressive bony overgrowth. If surgery is delayed too long, the condition may become inoperable. We hope that these recommendations will help clinicians gather appropriate data and assist their patients in making timely treatment decisions.

摘要

目的

美国国立卫生研究院(NIH)召开了一次多学科研讨会,以讨论变形综合征(PS)的骨科及其他并发症的管理,PS是一种进行性、不成比例的过度生长疾病。虽然PS带来了许多复杂挑战,但研讨会的重点是管理这种多系统疾病所特有的不对称且紊乱的骨骼过度生长。

方法

研讨会参与者制定了临床研究、患者管理及监测的建议,以最大限度地提高手术及其他干预措施的益处并降低风险。

结果

临床护理和管理建议包括通过X射线、磁共振成像(MRI)、双能X射线吸收法和计算机断层扫描(CT)成像等方式评估骨骼过度生长及其进展情况。这些建议还涵盖了对显著影响手术风险的PS非骨科并发症的评估,如肺栓塞和肺大疱。PS的手术考量包括评估挛缩对畸形的影响以及预防性软组织松解、积极早期使用骨骺阻滞术和骨骺固定术、截肢以及脊柱支具治疗。

结论

对于患有PS的儿童,骨科手术时机的决策具有挑战性,因为这需要在这个高风险且复杂的人群中权衡干预风险与患者因进行性骨过度生长而增加的发病率。如果手术延迟过长,病情可能会变得无法手术治疗。我们希望这些建议将有助于临床医生收集适当的数据,并协助他们的患者做出及时的治疗决策。