Pitfalls in the diagnosis of a tumefactive demyelinating lesion: A case report

<p>Abstract</p> <p>Introduction</p> <p>In rare instances, demyelinating disorders manifest as tumefactive lesions that simulate brain tumors. We report a patient with a space-occupying lesion in the parietal lobe, which presented a serious diagnostic dilemma, between a...

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Main Authors: Sakas Damianos, C Stavrinou Lampis, Boviatsis Efstathios, Gavra Maria
Format: Article
Language:English
Published: BMC 2011-06-01
Series:Journal of Medical Case Reports
Online Access:http://www.jmedicalcasereports.com/content/5/1/217
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spelling doaj-84fd06070ad74b6ebc92f42423f327c12020-11-24T22:10:05ZengBMCJournal of Medical Case Reports1752-19472011-06-015121710.1186/1752-1947-5-217Pitfalls in the diagnosis of a tumefactive demyelinating lesion: A case reportSakas DamianosC Stavrinou LampisBoviatsis EfstathiosGavra Maria<p>Abstract</p> <p>Introduction</p> <p>In rare instances, demyelinating disorders manifest as tumefactive lesions that simulate brain tumors. We report a patient with a space-occupying lesion in the parietal lobe, which presented a serious diagnostic dilemma, between a rare tumefactive demyelinating disease, such as Balo concentric sclerosis and a glioma. This case report highlights important diagnostic clues in the differential diagnosis of Balo concentric sclerosis.</p> <p>Case presentation</p> <p>A 20-year-old Caucasian woman with acute onset of left-sided weakness and numbness was admitted to hospital with neurologic signs of left-sided hemiparesis and hypoesthesia. Brain magnetic resonance imaging showed a mass lesion of abnormal signal intensity with concentric enhancing rings in the right parietal lobe, without perifocal edema. The characteristic concentric pattern detected on the magnetic resonance images was highly suggestive of Balo disease, and corticosteroids were administered. Evoked potentials, cerebrospinal fluid analysis, and magnetic spectroscopy findings were not specific, and glioma was also included in the differential diagnosis. A stereotactic biopsy was not diagnostic.</p> <p>After one month the patient showed moderate clinical improvement, and during 12 months follow-up, no further relapses occurred. In the follow-up magnetic resonance imaging, the concentric pattern had completely disappeared, and only a low-signal, gliotic lesion remained.</p> <p>Conclusion</p> <p>We hope this case presentation will advance our understanding of clinical and radiologic appearance of Balo concentric sclerosis, which is a rare demyelinating disease. Although this is a specific entity, it has a broader clinical impact across medicine, because it must be differentiated from other space-occupying lesions in the central nervous system.</p> http://www.jmedicalcasereports.com/content/5/1/217
collection DOAJ
language English
format Article
sources DOAJ
author Sakas Damianos
C Stavrinou Lampis
Boviatsis Efstathios
Gavra Maria
spellingShingle Sakas Damianos
C Stavrinou Lampis
Boviatsis Efstathios
Gavra Maria
Pitfalls in the diagnosis of a tumefactive demyelinating lesion: A case report
Journal of Medical Case Reports
author_facet Sakas Damianos
C Stavrinou Lampis
Boviatsis Efstathios
Gavra Maria
author_sort Sakas Damianos
title Pitfalls in the diagnosis of a tumefactive demyelinating lesion: A case report
title_short Pitfalls in the diagnosis of a tumefactive demyelinating lesion: A case report
title_full Pitfalls in the diagnosis of a tumefactive demyelinating lesion: A case report
title_fullStr Pitfalls in the diagnosis of a tumefactive demyelinating lesion: A case report
title_full_unstemmed Pitfalls in the diagnosis of a tumefactive demyelinating lesion: A case report
title_sort pitfalls in the diagnosis of a tumefactive demyelinating lesion: a case report
publisher BMC
series Journal of Medical Case Reports
issn 1752-1947
publishDate 2011-06-01
description <p>Abstract</p> <p>Introduction</p> <p>In rare instances, demyelinating disorders manifest as tumefactive lesions that simulate brain tumors. We report a patient with a space-occupying lesion in the parietal lobe, which presented a serious diagnostic dilemma, between a rare tumefactive demyelinating disease, such as Balo concentric sclerosis and a glioma. This case report highlights important diagnostic clues in the differential diagnosis of Balo concentric sclerosis.</p> <p>Case presentation</p> <p>A 20-year-old Caucasian woman with acute onset of left-sided weakness and numbness was admitted to hospital with neurologic signs of left-sided hemiparesis and hypoesthesia. Brain magnetic resonance imaging showed a mass lesion of abnormal signal intensity with concentric enhancing rings in the right parietal lobe, without perifocal edema. The characteristic concentric pattern detected on the magnetic resonance images was highly suggestive of Balo disease, and corticosteroids were administered. Evoked potentials, cerebrospinal fluid analysis, and magnetic spectroscopy findings were not specific, and glioma was also included in the differential diagnosis. A stereotactic biopsy was not diagnostic.</p> <p>After one month the patient showed moderate clinical improvement, and during 12 months follow-up, no further relapses occurred. In the follow-up magnetic resonance imaging, the concentric pattern had completely disappeared, and only a low-signal, gliotic lesion remained.</p> <p>Conclusion</p> <p>We hope this case presentation will advance our understanding of clinical and radiologic appearance of Balo concentric sclerosis, which is a rare demyelinating disease. Although this is a specific entity, it has a broader clinical impact across medicine, because it must be differentiated from other space-occupying lesions in the central nervous system.</p>
url http://www.jmedicalcasereports.com/content/5/1/217
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