Symptomatic, radiological and pathological involvement of the hypothalamus in neuromyelitis optica

S Viegas(John Radcliffe Hospital), Andrew Weir(John Radcliffe Hospital), M M Esiri(John Radcliffe Hospital), Wilhelm Küker(John Radcliffe Hospital), Patrick Waters(John Radcliffe Hospital), Maria Isabel Leite(John Radcliffe Hospital), Angela Vincent(John Radcliffe Hospital), Jacqueline Palace(John Radcliffe Hospital)
Journal of Neurology Neurosurgery & Psychiatry
May 15, 2009
Cited by 58Open Access
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Abstract

This study describes a young girl who presented with involuntary weight loss, spontaneous vomiting and behavioural change. Imaging confirmed hypothalamic and brainstem involvement. Routine investigations (including cerebrospinal fluid analysis and neuromyelitis optica IgG) were unhelpful. Biopsy of the hypothalamic lesion implicated an aggressive inflammatory aetiology. There was a response to conventional immunosuppression, while a further relapse responded to plasma exchange. She died 21 months after presentation. Postmortem examination was highly suggestive of neuromyelitis optica, which was subsequently confirmed following the identification of aquaporin 4 antibodies.


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