Abstract：
:A clinical of 37 patients suffering form Guillain-Baré syndrome has been carried out. Because of their unusual onset and clinical course, two of the cases are reported in full. The first case presented atypical onset modalities characterised by dysarthria, dysphonia and dysphagia with subsequent diplegia of the facial nerve and motor involvement of all four extremities; the second was difficult to diagnose and over time it turned out to be disimmune chronic-recurrent polyneuropathy. The clinic instrumental diagnostic and therapeutic course of this case, which was characterised by the poor response to corticosteroid therapy as a result of which use of immunosuppressor (azatioprine) and plasma-feresis were employed with a reaosable improvement, is described in detail. The differential diagnosis and nosologica classification are discussed.
journal_name
Minerva Medjournal_title
Minerva medicaauthors
Appiotti A,Trebini F,Scarzella Gsubject
Has Abstractpub_date
1990-10-01 00:00:00pages
727-9issue
10eissn
0026-4806issn
1827-1669journal_volume
81pub_type
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