Abstract | BACKGROUND: Schnitzler's syndrome is a rare etiology of chronic urticaria. The disease is characterized by the association of chronic urticaria, intermittent chronic fever, bone pain, osteosclerotic bone lesions and IgM monoclonal gammapathy. More than fifty patients with this syndrome have been reported since Schnitzler reported the first case in 1974, but neuropathies are seen only in a few cases. CASE REPORT: Our patient developed, eight years after the diagnosis of Schnitzler'syndrome, a peripheral sensitive neuropathy. Anti- myelin-associated glycoprotein antibodies were not significant. A nerve biopsy specimen has revealed aspecific demyelinization. Direct and indirect immunofluorescence were negative. We conclused is that our patient presented chronic inflammatory demyelinating polyneuropathy. DISCUSSION:
|
Authors | S Blaise, J-M Vallat, F Tabaraud, J-M Bonnetblanc |
Journal | Annales de dermatologie et de venereologie
(Ann Dermatol Venereol)
Vol. 130
Issue 3
Pg. 348-51
(Mar 2003)
ISSN: 0151-9638 [Print] France |
Vernacular Title | Syndrome de Schnitzler associé à une forme sensitive pure de polyradiculonévrite inflammatoire démyélinisante chronique. |
PMID | 12746673
(Publication Type: Case Reports, English Abstract, Journal Article)
|
Chemical References |
|
Topics |
- Aged
- Humans
- Immunoglobulin M
(analysis)
- Male
- Polyradiculoneuropathy, Chronic Inflammatory Demyelinating
(etiology, pathology)
- Schnitzler Syndrome
(complications)
|