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A case of periodic-fever-syndrome-like disorder with lipodystrophy, myositis, and autoimmune abnormalities.
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A 24-year-old Japanese woman had been suffering from a periodic fever since 10 months of age. She developed deformities in her fingers, with severe atrophy of subcutaneous adipose tissue, myositis, and frostbitten hands. She showed elevated C-reactive protein, creatine kinase, and gamma-globulin.
Myositis in a patient with familial Mediterranean fever and spondyloarthritis successfully treated with anakinra.
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Familial Mediterranean fever is an autosomal-recessive autoinflammatory disorder more commonly observed in Mediterranean populations and characterized by recurrent episodes of fever, serositis, myalgia and arthritis. There is rarely any association with spondyloarthritis. The most important
A novel missense mutation (C30S) in the gene encoding tumor necrosis factor receptor 1 linked to autosomal-dominant recurrent fever with localized myositis in a French family.
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OBJECTIVE
To characterize both phenotypic (clinical features and magnetic resonance imaging [MRI] findings) and genotypic aspects of autosomal-dominant recurrent fever, also known as tumor necrosis factor receptor (TNFR)-associated periodic syndrome (TRAPS), in a French family and to investigate the
Concurrent Guillain-Barré syndrome and myositis complicating dengue fever.
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Dengue is an arboviral infection that classically presents with fever, headache, joint pain, skin flush and morbilliform rashes. Neurological manifestations are well recognised but their exact incidence is unknown. Though myalgias are common in dengue virus infection, myositis and/or elevated serum
[Neonatal parechovirus infection, fever, irritability and myositis].
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Human parechovirus (HPeV) is associated with central nervous system infection and sepsis-like illness in newborn infants. The most frequent signs are fever, seizures, irritability, rash, and encephalitis. We report 4 cases of full-term infants with HPeV infection. They were admitted from home to the
Polyarteritis manifesting as calf myositis and fever.
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A patient presented with fever of undetermined cause for two months. On physical examination, bilateral calf tenderness was elicited, prompting a diagnostic muscle biopsy for polyarteritis. This limited form of polyarteritis is reviewed in the context of this case and previously reported cases.
Fever, Myositis, and Paralysis: Is This Inflammatory Myopathy or Neuroinvasive Disease?
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West Nile virus (WNV) is a mosquito-borne RNA Flavivirus which emerged in North America in 1999. Most patients present with a febrile illness but a few develop WNV neuroinvasive disease. Myopathy is an uncommon manifestation. We describe a case of a 42-year-old male from Los Angeles who presented
Focal Myositis of the Leg Presenting as Fever of Unknown Origin Detected by FDG PET/CT.
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Focal myositis is an uncommon inflammatory pseudotumor of the skeletal muscle that may mimic neoplastic and inflammatory diseases. We present one case of focal myositis involving the left proximal vastus lateralis and vastus intermedius, and left soleus showing intense FDG uptake on FDG PET/CT. This
[Myositis and rhabdomyolysis caused by Q fever].
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Tocilizumab is effective in a familial Mediterranean fever patient complicated with histologically proven recurrent fasciitis and myositis.
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[Myositis in mediterranean boutonneuse fever].
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Yellow Fever Vaccine as a Possible Trigger of Inflammatory Myopathy: A Case Report.
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Isolated myositis as a sole presentation of familial Mediterranean fever.
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[Fever and microhematuria. cANCA-glomerulonephritis with arthralgia, myositis and possible vasculitic involvement of the aortic valve].
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Histologic signs of inflammatory myopathy in familial Mediterranean fever.
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