Marburg’s variant multiple sclerosis (MS) is an acute and aggressive atypical form of MS, leading frequently to death in few months. A 32-year-old man with motor and sensory symptoms suggestive of acute myelopathy, rapidly followed by cerebellar dysfunction and consciousness impairment. Clinical, laboratory and radiological evaluations suggested a central nervous system demyelinating disease. The diagnosis was Marburg’s variant MS, usually leading to death in short time. He underwent different treatments, including steroids, cyclophosphamide, plasma exchange and lastly interferon-beta. The patient reached clinical stability with severe residual disability, persistent after 3 years from onset. This observation suggests that subjects with Marburg’s MS might reach long clinical stability.

Long survival and clinical stability in Marburg's variant multiple sclerosis.

TURATTI, Marco;GAJOFATTO, Alberto;Benedetti M. D.
2010-01-01

Abstract

Marburg’s variant multiple sclerosis (MS) is an acute and aggressive atypical form of MS, leading frequently to death in few months. A 32-year-old man with motor and sensory symptoms suggestive of acute myelopathy, rapidly followed by cerebellar dysfunction and consciousness impairment. Clinical, laboratory and radiological evaluations suggested a central nervous system demyelinating disease. The diagnosis was Marburg’s variant MS, usually leading to death in short time. He underwent different treatments, including steroids, cyclophosphamide, plasma exchange and lastly interferon-beta. The patient reached clinical stability with severe residual disability, persistent after 3 years from onset. This observation suggests that subjects with Marburg’s MS might reach long clinical stability.
2010
no
Inglese
STAMPA
Esperti anonimi
31
6
807
811
5
multiple sclerosis; Marburg's variant; long survival
https://doi.org/10.1007/s10072-010-0287-4
none
info:eu-repo/semantics/article
Turatti, Marco; Gajofatto, Alberto; Rossi, F.; Vedovello, M.; Benedetti, M. D.
5
01 Contributo in rivista::01.01 Articolo in Rivista
262
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11562/345370
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