Whipple's disease with muscle impairment
β Scribed by Marie Puget; Jean Iwaz; Anne Tristan; Nathalie Streichenberger
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 217 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0148-639X
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
A 67βyearβold man presented with myalgia, muscle atrophy, and a history of seronegative polyarthritis. Blood tests showed inflammation but no hematologic or immunologic abnormalities. Muscle biopsy revealed no vasculitis or myositis but Tropheryma whipplei was detected by polymerase chain reaction in muscle, blood, and duodenum specimens; this was confirmed by immunohistochemistry. Ceftriaxone led to clinical improvement. Although rare, Whipple's disease should be considered in the differential diagnosis of diffuse myopathy. Muscle Nerve, 2006
π SIMILAR VOLUMES
Impairment of muscle glycogenolysis in McArdle's disease (myophosphorylase deficiency) leads to exercise intolerance and exercise-induced myalgia. The pathophysiology of these symptoms is not entirely clear. We used phosphorus magnetic resonance spectroscopy to measure muscle phosphate metabolite co
Whipple's disease is an uncommon malabsorption disorder which is generally diagnosed by barium contrast studies, laboratory and histologic examin a t i o n ~. ~, ~. ~ Ultrasound has been recently recommended in the detection of gastrointestinal tumors, inflammatory and neoplastic infiltrations of th
We extend sincere congratulations to Dr Jacobs and colleagues for the successful conclusion of their study of recombinant interferon p l a (rIFN-pla) in patients with multiple sclerosis (MS). The impressive results showed that 6 million international units of rIFN-Pla applied once weekly via the int