Balo’s concentric sclerosis. A lecture describing six clinical cases

Balo’s concentric sclerosis (BCS) is a rare demyelinating disorder. The article analyzes six BCS cases diagnosed using magnetic resonance imaging, clinical data, and cerebrospinal fluid studies. The goal is to differentiate BCS from multiple sclerosis (MS), assess prognosis, and evaluate therapy. Patients exhibited concentric demyelination lesions. In two cases, oligoclonal antibodies were absent (type 1, typical for BCS), while others showed type 2 (more common in MS). Treatment included corticosteroids, plasmapheresis, and anti-B-cell therapy. Disease course varied: some patients had a monophasic course, while others experienced relapsing symptoms resembling pseudotumoral MS. Magnetic resonance imaging showed lesion reduction, but some patients retained neurological deficits.BCS may be a distinct nosological entity but requires careful differentiation from MS. Early imaging and cerebrospinal fluid analysis are crucial for diagnosis. MS-like therapy is effective, but further research is needed.

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Publication Details

Journal
Russian Journal of Child Neurology
Published
2025-08-04
DOI
https://doi.org/10.17650/2073-8803-2025-20-2-52-60
Primary Topic
Systemic Sclerosis and Related Diseases
Type
article
Field-Weighted Citation Impact
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article

Balo’s concentric sclerosis. A lecture describing six clinical cases

Anna A. Ershova, А. С. Котов, E. O. Ovchinnikova, A. N. Peshkin et al.
Russian Journal of Child Neurology
Systemic Sclerosis and Related Diseases
article

Balo’s concentric sclerosis. A lecture describing six clinical cases

Anna A. Ershova, А. С. Котов, E. O. Ovchinnikova, A. N. Peshkin, S. A. Syanov
article en

Abstract

Balo’s concentric sclerosis (BCS) is a rare demyelinating disorder. The article analyzes six BCS cases diagnosed using magnetic resonance imaging, clinical data, and cerebrospinal fluid studies. The goal is to differentiate BCS from multiple sclerosis (MS), assess prognosis, and evaluate therapy. Patients exhibited concentric demyelination lesions. In two cases, oligoclonal antibodies were absent (type 1, typical for BCS), while others showed type 2 (more common in MS). Treatment included corticosteroids, plasmapheresis, and anti-B-cell therapy. Disease course varied: some patients had a monophasic course, while others experienced relapsing symptoms resembling pseudotumoral MS. Magnetic resonance imaging showed lesion reduction, but some patients retained neurological deficits.BCS may be a distinct nosological entity but requires careful differentiation from MS. Early imaging and cerebrospinal fluid analysis are crucial for diagnosis. MS-like therapy is effective, but further research is needed.

Russian Journal of Child NeurologyVol. 20(2)
Regional Clinical Research (US), Federal Medical-Biological Agency (RU)
Openalex Percentile: Top 71%
Systemic Sclerosis and Related Diseases
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Balo’s concentric sclerosis. A lecture describing six clinical cases — Anna A. Ershova, А. С. Котов, et al. · Russian Journal of Child Neurology (2025) | TGRS Research Map | TGRS