A Case Report of Sensory Guillain-Barré Syndrome with Prominent Autonomic Dysfunction in a Systemic Lupus Erythematosus Patient / 대한신경근육질환학회지
Korean Journal of Neuromuscular Disorders
; (2): 38-41, 2022.
Article
em Ko
| WPRIM
| ID: wpr-968174
Biblioteca responsável:
WPRO
ABSTRACT
Sensory Guillain-Barré syndrome (GBS) is a rare heterogeneous subgroup of GBS characterized by the primary involvement of sensory neurons resulting in a distinctive clinical presentation. Sensory GBS usually occurs with acute and monophasic sensory symptoms, and no or minimal muscle weakness. Sensory GBS patient show hypo- or areflexia, distal paresthesia, and normal cerebrospinal fluid finding or albumino-cytologic dissociation which are suggesting that these conditions are a GBS variant. Autonomic dysfunctions have rarely been reported in sensory GBS patient presenting with postural hypotension, abnormal heart rate response to respiration. In this case, we demonstrate a patient with autonomic symptoms dominant sensory GBS in systemic lupus erythematosus.
Texto completo:
1
Base de dados:
WPRIM
Idioma:
Ko
Revista:
Korean Journal of Neuromuscular Disorders
Ano de publicação:
2022
Tipo de documento:
Article