Overproduction of vascular endothelial growth factor/vascular permeability factor is causative in crow-fukase (POEMS) syndrome
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...
Saved in:
Published in | Muscle & nerve Vol. 21; no. 11; pp. 1390 - 1397 |
---|---|
Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
New York
John Wiley & Sons, Inc
01.11.1998
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | 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 endothelial growth factor/vascular permeability factor (VEGF) in the serum and cerebrospinal fluid (CSF) from 10 patients with this syndrome. Serum VEGF levels were about 15–30 times those in control subjects or patients with Guillain–Barré syndrome (GBS), chronic inflammatory demyelinating polyneuropathy (CIDP), and other neurological disorders. The CSF VEGF levels, however, were similar to those found in GBS and CIDP. Elevated VEGF levels in the serum decreased in 7 patients with Crow–Fukase syndrome after conventional therapy. The principal isoform of VEGF in Crow–Fukase syndrome was VEGF165. Elevated VEGF was independent of M‐protein. Our results suggest that the overproduction of VEGF is important in the pathogenesis of this disorder. © 1998 John Wiley & Sons, Inc. Muscle Nerve 21: 1390–1397, 1998 |
---|---|
Bibliography: | ArticleID:MUS5 Japanese Ministry of Health and Welfare istex:1EF9829151BF46D3BD263763E6A063620C5F848D ark:/67375/WNG-N6SZG40F-S ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0148-639X 1097-4598 |
DOI: | 10.1002/(SICI)1097-4598(199811)21:11<1390::AID-MUS5>3.0.CO;2-4 |