Your browser doesn't support javascript.
loading
Rare occurrence of eight-and-a-half syndrome as a clinically isolated syndrome.
Jacob, Sneha; Murray, Ann.
Affiliation
  • Jacob S; Department of Neurology, West Virginia University Health Sciences Center, Morgantown, West Virginia, USA.
  • Murray A; Department of Neurology, West Virginia University Health Sciences Center, Morgantown, West Virginia, USA.
BMJ Case Rep ; 20182018 Jan 26.
Article in En | MEDLINE | ID: mdl-29374635
ABSTRACT
Eight-and-a-half syndrome is a rare condition that is described as a combination of one-and-a-half syndrome and an ipsilateral facial nucleus lesion. We present a clinical case of occurrence of eight-and-a-half syndrome that was caused by a demyelinating lesion in the dorsal pontine tegmentum. A 44-year-old man presented to the hospital with a subacute onset of horizontal diplopia and left-sided facial weakness. MRI revealed a T2 hyperintense lesion in his dorsal pons, which was consistent with a demyelinating pathology. Treatment with intravenous steroids showed significant improvement in his symptoms. In our case, it occurred due to a suspected demyelinating lesion that was this patient's first and only demyelinating event, leaving him with a diagnosis of clinically isolated syndrome. His responsiveness to steroids represents the first case report of an adult patient presenting with an eight-and-a-half syndrome secondary to a suspected demyelinating pathology.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Ophthalmoplegia / Demyelinating Diseases / Stroke, Lacunar / Pontine Tegmentum Type of study: Etiology_studies Limits: Adult / Humans / Male Language: En Journal: BMJ Case Rep Year: 2018 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Ophthalmoplegia / Demyelinating Diseases / Stroke, Lacunar / Pontine Tegmentum Type of study: Etiology_studies Limits: Adult / Humans / Male Language: En Journal: BMJ Case Rep Year: 2018 Document type: Article Affiliation country: United States