A rare presentation of atypical demyelination: tumefactive multiple sclerosis causing Gerstmann’s syndrome

BMC Neurology - Tập 14 - Trang 1-5 - 2014
Sharmilee Gnanapavan1,2, Zane Jaunmuktane3, Kelly Pegoretti Baruteau4, Sakthivel Gnanasambandam4, Klaus Schmierer1,2
1Blizard Institute, Barts and The London School of Medicine & Dentistry, Queen Mary, University of London, London, UK
2Department of Neurology, Barts Health NHS Trust, The Royal London Hospital, London, UK
3Division of Neuropathology, UCLH Foundation Trust, The National Hospital for Neurology & Neurosurgery, London, UK
4Department of Neuroradiology, Barts Health NHS Trust, The Royal London Hospital, London, UK

Tóm tắt

Tumefactive demyelinating lesions are a rare manifestation of multiple sclerosis (MS). Differential diagnosis of such space occupying lesions may not be straightforward and sometimes necessitate brain biopsy. Impaired cognition is the second most common clinical manifestation of tumefactive MS; however complex cognitive syndromes are unusual. We report the case of a 30 year old woman who presented with Gerstmann’s syndrome. MRI revealed a large heterogeneous contrast enhancing lesion in the left cerebral hemisphere. Intravenous corticosteroids did not stop disease progression. A tumour or cerebral lymphoma was suspected, however brain biopsy confirmed inflammatory demyelination. Following diagnosis of tumefactive MS treatment with natalizumab effectively suppressed disease activity. The case highlights the need for clinicians, radiologists and surgeons to appreciate the heterogeneous presentation of tumefactive MS. Early brain biopsy facilitates rapid diagnosis and management. Treatment with natalizumab may be useful in cases of tumefactive demyelination where additional evidence supports a diagnosis of relapsing MS.

Tài liệu tham khảo

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