All Restricted Spines are not Spondyloarthritis: Fibrodysplasia Ossificans Progressiva (FOP) in Monozygotic Twins presenting to Rheumatology Clinic.

Q4 Medicine
Mediterranean Journal of Rheumatology Pub Date : 2025-01-08 eCollection Date: 2025-03-01 DOI:10.31138/mjr.210524.mta
Avanish Jha, Noel Deep Luke, Aditya Nair, Ajith Sivadasan, Sumita Danda
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Abstract

Fibrodysplasia ossificans progressiva (FOP) is a rare and progressive debilitating disease that is often misdiagnosed. We present FOP in monozygotic twins in their teen years, presenting to an adult rheumatology outpatient clinic with restricted neck and spine and a referral to rule out ankylosing spondylitis. The classical feature of recurrent episodes of painful lumps on their body, along with classical deformity of their big toes and radiography, clinched the clinical diagnosis. This was further confirmed by a genetic analysis. We review here the pathogenesis and literature on newer treatment options for FOP. The first FDA-approved drug, palovarotene, was approved in 2023. It showed a reduction in heterotopic ossifications. This highlights the need for awareness of this condition among both adult and paediatric rheumatologists so that harmful biopsies and surgeries can be avoided, and patients can start on newer therapies early in the disease. It can be considered a rare mimic of ankylosing spondylitis; however, the characteristic features can very well identify the disorder clinically.

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并非所有限制性脊柱都是脊椎关节炎:向风湿病诊所报告的同卵双胞胎进行性骨化纤维发育不良(FOP)。
进行性骨化性纤维发育不良(FOP)是一种罕见的进行性衰弱疾病,经常被误诊。我们在青少年时期的同卵双胞胎中提出FOP,在成人风湿病门诊就诊,颈部和脊柱受限,并转诊排除强直性脊柱炎。他们身上疼痛的肿块反复发作的典型特征,以及大脚趾的典型畸形和x线摄影,确定了临床诊断。基因分析进一步证实了这一点。我们在此回顾该病的发病机制和最新治疗方案的文献。fda批准的第一种药物palovarotene于2023年获得批准。它显示异位骨化的减少。这突出了成人和儿科风湿病学家对这种情况的认识的必要性,以便避免有害的活组织检查和手术,并且患者可以在疾病早期开始新的治疗。它可以被认为是一种罕见的强直性脊柱炎的模拟物;然而,这些特征在临床上可以很好地识别疾病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.00
自引率
0.00%
发文量
42
审稿时长
8 weeks
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