Clinical and radiological characteristics of tumefactive demyelinating lesions: follow-up study

Author:

Altintas A1,Petek B2,Isik N3,Terzi M4,Bolukbasi F1,Tavsanli M1,Saip S1,Boz C5,Aydin T3,Arici-Duz O3,Ozer F2,Siva A1

Affiliation:

1. Department of Neurology, Istanbul University, Turkey

2. Department of Neurology, Haseki Training and Research Hospital, Istanbul, Turkey

3. Department of Neurology, Goztepe Training and Research Hospital, Istanbul, Turkey

4. Department of Neurology, Ondokuz Mayıs University, Samsun, Turkey

5. Department of Neurology, Karadeniz Technical University, Trabzon, Turkey

Abstract

Background: Demyelinating lesions over 20 mm in size, referred to as tumefactive demyelinating lesions, can be misdiagnosed as being either a tumor or an abscess. Although some radiological characteristics can help make a differential diagnosis easier, a cerebral biopsy may still be necessary. Objective: Our objective was to assess the clinical characteristics of tumefactive lesions, with or without a diagnosis of multiple sclerosis (MS), and present follow-up data for 54 patients with tumefactive lesions. Methods: Demographic, clinical, radiological and laboratory data were gathered and treatment responses were evaluated in a total of 54 patients from five medical centers. Result: Twenty-nine patients were diagnosed with tumefactive lesions at the onset, whereas 25 patients were diagnosed with tumefactive lesions after a diagnosis of MS. Median follow-up was 38.12 months. At final examination, 19 of the patients with a tumefactive lesion diagnosis at the onset eventually developed relapsing–remitting MS, while 10 remained with the condition as a clinically isolated syndrome. The tumefactive lesions studied were mostly focal, with closed-ring enhancement. We found that oligoclonal band positivity was less frequent in the patients with tumefactive onset. Conclusion: Although our demographic data were similar to formerly collected Turkish MS data, we found that the distribution of the patients’ clinical course differed if there was an absence of primary progressive MS and that there was a lower frequency of secondary progressive MS cases in our group of patients. We believe that less frequent oligoclonal band positivity and the difference we witnessed in the clinical course of disease in our study groups suggest that there is a need for further studies to compare all the biological and immunological differences between MS and tumefactive lesion cases, in order to reveal whether there are different pathogenetic mechanisms involved.

Publisher

SAGE Publications

Subject

Neurology (clinical),Neurology

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