Pagine elettroniche
La sindrome di Guillain-Barré con parestesie e diplegia facciale. Descrizione di un caso clinico
Guillain-Barré syndromewith paresthesias and facial diplegia. A case report
C. Domenicali, C. Farneti, A. Magistà, F. Pugliese, S. Pusceddu, L. Casadio, A. Pini, F. Marchetti
Dicembre 2015 - pagg. 663 -664
Abstract
Acute bilateral facial nerve palsy is a relatively rare
condition and often indicates a serious underlying medical condition.
The paper reports a case of a 14-year-old girl who developed
paresthesias in the distal limbs and subsequently bifacial
weakness, dysphonia and dysphagia. She had had a preceding
episode of upper tract respiratory infection. Neurological examination
showed severe facial diplegia. Limb muscle power was
preserved. Cerebrospinal fluid showed albumin cytological dissociation.
Magnetic Resonance Imaging scan of the head was
normal. Intravenous immunoglobulin (2 g/kg for a 5-day period)
was started. The abnormal sensation in her lower limb almost
disappeared, dysphonia and dysphagia rapidly improved after
the second infusion. Oral steroid therapy was also added. The
residual bilateral facial palsy recovered completely after 6
weeks. Bifacial weakness with paresthesias (BFP) is a subtype of
Guillain-Barré syndrome and it is defined by rapidly progressive
bilateral facial weakness in the absence of other cranial nerve
involvement. Since this condition shows a rapid responsivity to
immunogloubulins treatment, a prompt diagnosis is important.
Classificazione MeSH
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Corrispondenza: federico.marchetti@ausl.ra.it
