史无前例的自体炎性肌炎和慢性血栓形成与杂合子 M694V 突变共存:家族性地中海热的非典型表现。

IF 0.9 Q4 RHEUMATOLOGY
Furkan Bahar, Serdal Ugurlu
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引用次数: 0

摘要

家族性地中海热(FMF)是一种遗传性自身炎症性疾病,主要特征是周期性发热、腹痛和关节表现。该病可表现出多种非典型症状,患者遍布全球。然而,FMF 同时伴有慢性血栓形成和肌炎的病例此前尚未见报道。一名 41 岁的男性患者出现双侧交替性剧烈腿痛、僵硬和局部肿胀,但无发热或腹部症状。他的病史包括反复发作的关节炎性疼痛,曾用泼尼松龙治疗。体格检查发现腿部疼痛,踝关节活动受限,大腿、前臂和足部有触痛性肿胀。此外,还观察到腹侧静脉。患者对泼尼松龙和秋水仙碱无反应,接受了核磁共振检查,发现双腿和大腿肌肉发炎,肾下下腔静脉有慢性血栓形成。基因检测证实了杂合子 M694V 突变,诊断为非典型 FMF。经过 Anakinra 治疗后,患者的临床和实验室指标均有明显改善。尽管 FMF 的诊断通常依赖于特征性临床特征和基因分析,但非典型表现对既定标准提出了挑战。本病例独特地展示了 FMF 中并存的肌炎和慢性血栓形成。肌痛在 FMF 中很常见,M694V 突变与严重的肌肉症状有关。我们的病例没有发热,也没有肌炎,这使其有别于长期发热性肌痛综合征。众所周知,FMF 的慢性炎症状态会影响血栓形成的风险,而我们的研究结果也与这一关联相吻合。慢性血栓栓塞症和肌炎共同构成了 FMF 不寻常的临床表现。该病例突出表明,FMF 可能会出现超出常规症状的复杂表现。结合患者病史、临床特征和实验室结果,肌炎和血管受累应考虑诊断为 FMF。这些罕见的关联强调了进一步研究的必要性,以加深对 FMF 多样化临床表现的了解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Unprecedented coexistence of autoinflammatory myositis and chronic thrombosis with heterozygotic M694V mutation: An atypical presentation of familial Mediterranean fever.

Familial Mediterranean Fever (FMF) is a hereditary autoinflammatory disorder predominantly characterised by periodic fever, abdominal pain, and joint manifestations. It can exhibit various atypical presentations. However, cases of FMF concurrently presenting with chronic thrombosis and myositis have not been previously reported. A 41-year-old male presented with alternating severe bilateral leg pain, stiffness, and localised swellings without fever or abdominal symptoms. His history included inflammatory joint pain treated with prednisolone. Physical examination revealed leg pain, limited ankle joint movement, and tender swellings in thighs, forearms, and feet. Collateral abdominal veins were also observed. Unresponsive to prednisolone and colchicine, the patient underwent MRI, revealing muscle inflammation in both legs and thighs and chronic thrombosis in the infrarenal inferior vena cava. Genetic testing confirmed the heterozygotic M694V mutation, diagnosing an atypical FMF. This case uniquely showcases coexisting myositis and chronic thrombosis in FMF. Myalgia is common in FMF, with M694V mutation associated with severe muscular symptoms. The lack of fever and myositis findings differentiate our case from protracted febrile myalgia syndrome. FMF's chronic inflammatory state is known to influence thrombosis risk, and our findings align with this association. Chronic thromboembolism and myositis together signify an unusual clinical presentation of FMF. This case highlights the potential for FMF to present with complex manifestations beyond the conventional symptoms. Myositis and vascular involvement should prompt consideration of FMF diagnosis when combined with patient history, clinical features, and laboratory results. These rare associations underscore the need for further research to enhance understanding of FMF's diverse clinical spectrum.

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