Rabdomiolise e mioglobinuria: relato de caso agudo com boa evolução


Autoria(s): Pinto, Osiris Esteves; Agapejev, Svetlana; Nóbrega, João Antonio Maciel
Contribuinte(s)

Universidade Estadual Paulista (UNESP)

Data(s)

20/05/2014

20/05/2014

01/09/1983

Resumo

Os autores registram um caso de mioglobinúria confirmada pela eletroforese de proteínas da urina. A eletromiografia revelou alterações de tipo polimiosítico. A biópsia muscular do deltóide esquerdo mostrou processo inflamatório muscular inespecífico. O tratamento instituído baseou-se em repouso, hiperhidratação e alcalinização da urina. Os autores enfatizam a importância do diagnóstico pela relativa benignidade do processo, que tende para a cura se forem superadas as sérias complicações da fase aguda, a iatrogenia medicamentosa e por procedimentos diagnósticos desnecessários no início da doença.

A case of paroxysmal myoglobinuric myopathy diagnosed by urinary protein electrophoresis is reported. Electromyograph (EMG) study done 20 days after onset of the symptoms demonstrated a polimyositic feature with normal motor and sensitive nervous conduction pattern. A biopsy of the left deltoid muscle performed 3 days after the EMG showed only an inespecific inflammation. The treatment included bed rest, parenteral fluids administration in excess (about 3,000 ml per day) and urinary alkalinization. Recovery started on the 2nd day of hospitalization when the patient showed progressive decrease in pain and weakness; furthermore the patient reacquired his mobility. The myoglobinuria start diminishing in intensity on the third day. The clinical picture of the patient continued to improve in the next 2 weeks, and slow recovery of the muscular strength occurred during the following two months of convalescence. In the present case we were not able to stablish the etiology of the illness. Nevertheless the clinical history suggests that infection, allergy and/or parenteral drug administration have had some role in precipitating the disease. This case report reinforces the concept that it is necessary an early and precise diagnosis of this syndrome followed by an adequate therapeutic approach avoiding the unnecessary use of drugs which per se could aggravate the disease.

Formato

280-286

Identificador

http://dx.doi.org/10.1590/S0004-282X1983000300009

Arquivos de Neuro-Psiquiatria. Academia Brasileira de Neurologia - ABNEURO, v. 41, n. 3, p. 280-286, 1983.

0004-282X

http://hdl.handle.net/11449/12404

10.1590/S0004-282X1983000300009

S0004-282X1983000300009

S0004-282X1983000300009.pdf

Idioma(s)

por

Publicador

Academia Brasileira de Neurologia (ABNEURO)

Relação

Arquivos de Neuro-Psiquiatria

Direitos

openAccess

Tipo

info:eu-repo/semantics/article