2013
DOI: 10.1590/s0034-70942013000100010
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Uso de sugamadex em doença de Strumpell-Lorrain: relato de dois casos

Abstract: Content: Strumpell-Lorrain disease -or familial spastic paraplegia (FSP) -is a rare hereditary neurological disorder, mainly characterized by variable degrees of stiffness and weakening of the muscles, with cognitive impairment, deafness, and ataxia in the more severe cases. We describe two female siblings with FSP programmed for cholecystectomy and subtotal colectomy, respectively, and also how we dealt with the anesthetic management in both cases and review the literature on this disease in relation to anest… Show more

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“…A paraparesia espástica é o sinal clínico mais grave e incapacitante da PEH (ROE, 1963;FINK, 2006;VIEIRA;AILY, 2007). Por alguns autores é denominada como doença de Strümpell-Lorrain (MC DERMOTT et al, 2000;FRANCO-HERNÁNDEZ et al,2013).…”
Section: Paraparesia Espástica Hereditáriaunclassified
“…A paraparesia espástica é o sinal clínico mais grave e incapacitante da PEH (ROE, 1963;FINK, 2006;VIEIRA;AILY, 2007). Por alguns autores é denominada como doença de Strümpell-Lorrain (MC DERMOTT et al, 2000;FRANCO-HERNÁNDEZ et al,2013).…”
Section: Paraparesia Espástica Hereditáriaunclassified