Coagulation and vascular abnormalities were studied in 4 patients with Crow-Fukase syndrome (CFS or POEMS) to understand the pathophysiology. Fibrinogen, fibrinopeptide A, and thrombin-antithrombin complexes (TAT) increased in sera during active phase of CFS. In nerves of 2 untreated cases, the endo
Cytokines and myelin antibodies in Crow-Fukase syndrome
β Scribed by Kyoko Saida; Mitsuhiro Ohta; Hideshi Kawakami; Takahiko Saida
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 254 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0148-639X
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β¦ Synopsis
syndrome (CFS) ,z~11~'z~18 or PO-EMS syndrome,' consists of polyneuropathy, organomegaly, endocrinopathy, plasma cell dyscrasia, skin changes, edema, and bone lesions. The increase of interleukin (IL)-lp,326 IL-63,5,6,10 and tumor necrosis factor (TNF)-a4 were reported in the sera of some patients with this syndrome, and the levels of these cytokines correlated to the clinical course of CFS. IL-6 contributes to the final maturation and differentiation of B lymphocytes into plasma cells.' However, it is not known whether these cytokines play important roles in inducing core symptoms such as polyneuropathy and edema in CFS. Most studies are based on a few cases or do not have well-matched disease controls.
In the present study, we measured the levels of these cytokines in sera from patients with CFS as well as rheumatoid arthritis (RA) and progressive systemic sclerosis (PSS) .
Further, to elucidate myelin and axon damages in CFS, we also assayed myelin or axon-related antibodies, including anti-GalCer and GM1, that are present in Guillain-BarrC syndrome," multifocal motor n e ~r o p a t h y , ' ~ and paraproteinemic polyneuropathy.g
Methods
Five patients with the diagnosis of CFS1' and who had proven nerve biopsies were taken into this study.
π SIMILAR VOLUMES
An earlier investigation from our laboratory (Ilyas AA, Willison HJ, Quarles RH, et al. Serum antibodies to gangliosides in Guillain-Barre syndrome. Ann Neurol 1988;23:440-447) demonstrating the presence of high levels of antiganglioside antibodies in the sera of 5 of 26 patients with Guillain-Barre
Crow-Fukase or POEMS syndrome of polyneuropathy, organomegaly, endocrinopathy, M-protein, and skin changes is a rare multisystem disorder of obscure pathogenesis that is associated with microangiopathy, neovascularization, and accelerated vasopermeability. We examined the levels of the vascular endo