7个月大的脊柱侧凸可能是进行性假性类风湿发育不良的表现吗?一份病例报告。

IF 0.8 Q3 MEDICINE, GENERAL & INTERNAL
Omran Janoud, Shihab Chaer, Yaman Shikha, Basheer Khalil
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引用次数: 0

摘要

背景:进行性假性类风湿发育不良是一种罕见的遗传性骨骼疾病,通常影响3至8岁的儿童。进行性假性类风湿发育不良的病理进展包括关节软骨的非炎性变性,导致进行性关节僵硬和增大。以前发表的研究没有认为脊柱侧凸是进行性假性类风湿发育不良的早期表现。然而,这篇论文做到了这一点,并说明了为什么我们应该把进行性假性类风湿发育不良作为早期脊柱侧凸的鉴别诊断。病例介绍:在本文中,我们报告了一名11岁的叙利亚阿拉伯女孩进行性假性类风湿发育不良,其表现为多个关节被动和主动运动的进行性限制。患者报告出现早期症状,包括7个月大时观察到的腰椎侧凸。然而,当时医生们无法做出明确的诊断。在与不同的医生进行了数年的随访后,病人到大马士革的儿童医院寻求治疗,在那里终于得到了准确的诊断。拍摄了新的x射线图像,并与以前的图像进行了比较,并进行了适当的实验室测试。根据所有现有资料,由于国内没有遗传分析,在没有进行遗传分析的情况下诊断了进行性假性类风湿发育不良。结论:我们撰写了这一病例报告,以指导未来的研究,以确定生命第一年的脊柱侧凸与进行性假性类风湿发育不良之间是否存在可能的联系。因此,是否值得考虑将进行性假性类风湿发育不良作为早期脊柱侧凸的鉴别诊断?
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Could scoliosis at the age of 7 months be a manifestation of progressive pseudorheumatoid dysplasia? A case report.

Background: Progressive pseudorheumatoid dysplasia is a rare genetic skeletal disease that usually affects children between the ages of 3 and 8 years. The pathological progression of progressive pseudorheumatoid dysplasia involves noninflammatory degeneration of the articular cartilage, resulting in progressive joint stiffness and enlargement. Previously published studies have not considered scoliosis as an early manifestation of progressive pseudorheumatoid dysplasia. However, this paper did, and showed why we should take progressive pseudorheumatoid dysplasia as a differential diagnosis if there is a scoliosis in early years of life.

Case presentation: In this paper, we report on an 11-year-old Syrian Arab girl with progressive pseudorheumatoid dysplasia who presented with progressive limitations in passive and active movement of multiple joints. The patient reported experiencing early symptoms, including lumbar scoliosis observed at the age of 7 months. However, at that time, the doctors were unable to make a definitive diagnosis. After years of follow-up with various doctors, the patient sought treatment at the Children's Hospital in Damascus, where an accurate diagnosis was finally reached. New X-ray images were taken and compared with previous ones, and appropriate laboratory tests were also conducted. Based on all the available information, a diagnosis of progressive pseudorheumatoid dysplasia was made without performing genetic analysis owing to its unavailability in the country.

Conclusion: We have written this case report to guide future studies in determining whether there is a possible link between scoliosis in the first years of life and progressive pseudorheumatoid dysplasia. Consequently, is it worth considering progressive pseudorheumatoid dysplasia as a differential diagnosis for scoliosis in the early years?

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来源期刊
Journal of Medical Case Reports
Journal of Medical Case Reports Medicine-Medicine (all)
CiteScore
1.50
自引率
0.00%
发文量
436
期刊介绍: JMCR is an open access, peer-reviewed online journal that will consider any original case report that expands the field of general medical knowledge. Reports should show one of the following: 1. Unreported or unusual side effects or adverse interactions involving medications 2. Unexpected or unusual presentations of a disease 3. New associations or variations in disease processes 4. Presentations, diagnoses and/or management of new and emerging diseases 5. An unexpected association between diseases or symptoms 6. An unexpected event in the course of observing or treating a patient 7. Findings that shed new light on the possible pathogenesis of a disease or an adverse effect
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