Severe Locked-In-Like Guillain-Barré's Syndrome: Dilemmas in Diagnosis and Treatment.
Rudolf KorinthenbergMatthias EckenweilerHans FuchsPublished in: Neuropediatrics (2020)
Guillain-Barré's syndrome in childhood can follow an atypical course, increasing the challenges in diagnosis and decisions regarding immunomodulatory treatment. Here, we report the case of on a 13-year-old boy with acute onset Guillain-Barré's syndrome progressing over 40 days to a very severe, locked-in-like syndrome despite intensive immunomodulatory treatment. After a plateau phase lasting 3 months and characterized by fluctuating signs of ongoing inflammatory disease activity, we were prompted to perform repeated and maintenance immunomodulatory treatment, which resulted in a continuous and nearly complete recovery of function. Atypical features at disease onset, the severe "total" loss of all peripheral and cranial nerve function, and an apparent late response to treatment give rise to reviewing the dilemmas of diagnosis and treatment in such severe and protracted courses of Guillain-Barré syndrome.
Keyphrases
- disease activity
- case report
- rheumatoid arthritis
- systemic lupus erythematosus
- early onset
- combination therapy
- drug induced
- computed tomography
- hepatitis b virus
- magnetic resonance
- replacement therapy
- extracorporeal membrane oxygenation
- juvenile idiopathic arthritis
- rheumatoid arthritis patients
- liver failure
- aortic dissection