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靠近骨的先天性伪:一个病例报告

Jiewei Weng¹, Jiaqi Wang¹, Tianyou Li¹

¹Department of Pediatric Orthopedics, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, Shandong, China.

Frontiers in pediatrics

|February 16, 2026

概括

这项研究详细介绍了一例罕见的近端部伪,该病例发生在患有神经纤维素型1的儿童身上. 治疗涉及手术和骨移植,导致成功结合和形纠正.

科学领域:

儿科整形外科儿科整形外科
遗传学是一个遗传学.
骨发育不良症骨发育不良症

背景情况:

骨先天性伪 (CPT) 是一种罕见的儿科骨科疾病.
靠近部的CPT异常罕见,现有的文献有限.
1型神经纤维素瘤病与各种骨科并发症有关.

研究的目的:

报告一名儿科患者近端骨CPT与发育不良的独特病例.
描述这种罕见的表现的手术管理和结果.
提出一个关于近端骨CPT病因的假设,并支持标准化护理.

主要方法:

术术切除伪关节炎.
骨移植和内部固定 (拉什棒和板).
用于纠正骨质发生的Hemiepiphysiodesis.

主要成果:

伪关节的成功初始结合.
纠正与之相关的关节形变形.
对近端骨CPT的可行治疗方法的演示.

结论:

靠近部的CPT,虽然很少见,但可以有效地使用已确立的CPT原则来管理.
这个案例提供了对近道骨CPT的潜在形成机制的见解.
标准化诊断和管理策略对于CPT至关重要,包括罕见的近位变异.

关键词:

孩子们的孩子们的孩子们的孩子们骨的先天性伪硬性.在近距离的CPT.靠近的小腿椎形症.手术手术手术手术手术手术手术

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