Familial Mediterranean fever presenting with protracted febrile myalgia: a case report.

C. Ozturk, S. Sutçuoglu, E. Ozer, S. Akman
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Abstract

The clinical spectrum of familial Mediterranean fever (FMF) expanded especially in the last fifteen years, so “protracted febrile myalgia” is now considered as one of the clinical manifestations of the FMF. We present a 12-year-old girl who was admitted to the Pediatrics Clinic with fever and severe myalgia in her upper and lower extremities lasting for 10 days before the diagnosis of FMF. Her genetic diagnosis was homozygosity for M694V mutation. We emphasize that protracted febrile myalgia in some cases of FMF could be the first symptom during childhood. The case was presented with the review of the literature.
家族性地中海热表现为持续性发热性肌痛:1例报告。
家族性地中海热(FMF)的临床谱在过去15年中扩大,因此“持续性发热性肌痛”现在被认为是FMF的临床表现之一。我们报告一名12岁的女孩,在诊断为FMF之前,因发烧和下肢严重肌痛持续10天而被儿科诊所收治。基因诊断为M694V突变纯合子。我们强调,长期发热性肌痛在某些情况下,FMF可能是儿童时期的第一个症状。该病例与文献综述一起提出。
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