TY - JOUR
T1 - Bickerstaff's brainstem encephalitis with overlapping Guillain-Barré syndrome
T2 - Usefulness of sequential nerve conduction studies
AU - Fong, Choong Yi
AU - Aung, Hnin Wint Wint
AU - Khairani, Arie
AU - Gan, Chin Seng
AU - Shahrizaila, Nortina
AU - Goh, Khean Jin
N1 - Publisher Copyright:
© 2018 The Japanese Society of Child Neurology
PY - 2018/6
Y1 - 2018/6
N2 - Bickerstaff's brainstem encephalitis (BBE) is a rare immune-mediated disorder characterized by ophthalmoplegia, ataxia and disturbance of consciousness, which may overlap with Guillain-Barré syndrome (GBS) if there is additional limb weakness. We report a 7-month-old boy presented with ophthalmoplegia followed by a rapidly ascending paralysis of all four limbs and disturbance of consciousness. The initial impression was BBE with overlapping GBS. This was supported by sequential nerve conduction study (NCS) findings compatible with an acute inflammatory demyelinating polyneuropathy (AIDP). He received intravenous pulse methylprednisolone, intravenous immunoglobulin and plasmapharesis with complete clinical recovery after 6 weeks of illness and improved NCS findings from week 16. This is the first case of paediatric BBE with overlapping GBS with an AIDP subtype of GBS. It expands the clinical spectrum of this condition in children. Our case highlights the importance of sequential NCS in paediatric BBE with overlapping GBS for accurate electrophysiological diagnosis and prognosis particularly if the first NCS findings are not informative.
AB - Bickerstaff's brainstem encephalitis (BBE) is a rare immune-mediated disorder characterized by ophthalmoplegia, ataxia and disturbance of consciousness, which may overlap with Guillain-Barré syndrome (GBS) if there is additional limb weakness. We report a 7-month-old boy presented with ophthalmoplegia followed by a rapidly ascending paralysis of all four limbs and disturbance of consciousness. The initial impression was BBE with overlapping GBS. This was supported by sequential nerve conduction study (NCS) findings compatible with an acute inflammatory demyelinating polyneuropathy (AIDP). He received intravenous pulse methylprednisolone, intravenous immunoglobulin and plasmapharesis with complete clinical recovery after 6 weeks of illness and improved NCS findings from week 16. This is the first case of paediatric BBE with overlapping GBS with an AIDP subtype of GBS. It expands the clinical spectrum of this condition in children. Our case highlights the importance of sequential NCS in paediatric BBE with overlapping GBS for accurate electrophysiological diagnosis and prognosis particularly if the first NCS findings are not informative.
KW - Acute inflammatory demyelinating polyneuropathy
KW - Bickerstaff's brainstem encephalitis
KW - Gullain-Barré syndrome
KW - Nerve conduction study
UR - http://www.scopus.com/inward/record.url?scp=85042117503&partnerID=8YFLogxK
U2 - 10.1016/j.braindev.2018.02.001
DO - 10.1016/j.braindev.2018.02.001
M3 - Article
C2 - 29459060
AN - SCOPUS:85042117503
SN - 0387-7604
VL - 40
SP - 507
EP - 511
JO - Brain and Development
JF - Brain and Development
IS - 6
ER -