Evidence map›Paper›PMID 40426809›Full record

ArticleChildren (Basel, Switzerland)2025

Overtime Challenges of Diagnosis and Treatment in Two Pediatric Patients with Extensive Cerebral Tumefactive Lesions Indicative of Baló's Type Multiple Sclerosis.

Alice Denisa Dică, Dana Craiu, Catrinel Iliescu, Marcel-Alexandru Găină, Carmen Sandu, Cristina Pomeran, Carmen Burloiu, Alexandra-Maria Găină, Daniela Adriana Ion

Abstract readCase Reports
In one paragraph

Article in Children (Basel, Switzerland), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Alice Denisa Dică"Prof. Dr. Alexandru Obregia" Clinical Hospital of Psychiatry, 041914 Bucharest, Romania.
Dana Craiu"Prof. Dr. Alexandru Obregia" Clinical Hospital of Psychiatry, 041914 Bucharest, Romania.
Catrinel Iliescu"Prof. Dr. Alexandru Obregia" Clinical Hospital of Psychiatry, 041914 Bucharest, Romania.
Marcel-Alexandru Găină3rd Medical Department, Psychiatry, The Faculty of Medicine, University of Medicine and Pharmacy "Grigore T. Popa", University Street Nr. 10, 700115 Iași, Romania.ORCID 0000-0003-0533-9014
Carmen Sandu"Prof. Dr. Alexandru Obregia" Clinical Hospital of Psychiatry, 041914 Bucharest, Romania.
Cristina Pomeran"Prof. Dr. Alexandru Obregia" Clinical Hospital of Psychiatry, 041914 Bucharest, Romania.
Carmen Burloiu"Prof. Dr. Alexandru Obregia" Clinical Hospital of Psychiatry, 041914 Bucharest, Romania.
Alexandra-Maria Găină3rd Medical Department, Psychiatry, The Faculty of Medicine, University of Medicine and Pharmacy "Grigore T. Popa", University Street Nr. 10, 700115 Iași, Romania.ORCID 0009-0004-8374-4255
Daniela Adriana IonDepartment of Pediatric Neurology, The Faculty of Medicine, "Carol Davila" University of Medicine and Pharmacy, 020021 Bucharest, Romania.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBaló's concentric sclerosis stands out as a rare form of multiple sclerosis that features large tumor-like demyelinating lesions, which resemble brain tumors and create significant diagnostic and therapeutic obstacles for pediatric patients. CASE PRESENTATIONS: We present two case studies of pediatric patients, aged 11 and 15, diagnosed with extensive cerebral tumefactive inflammatory lesions indicative of Balo's type multiple sclerosis (MS). Both cases highlight the unique challenges faced in the diagnosis and treatment of this rare form of MS, characterized by the presence of large, tumor-like lesions that can mimic primary brain tumors. We will explore the diagnostic complexities, including the need for advanced imaging techniques, MR (Magnetic Resonance) spectroscopy, along with the time needed for differential diagnoses, which might delay the start of proper treatment. Current therapies, such as corticosteroids and immunomodulators, require customization to individual patients, carefully monitoring of clinical outcomes and possible side effects. This paper emphasizes that handling these cases requires a multidisciplinary approach, addressing not only the medical treatment but also the psychosocial needs of affected children and their families. By sharing these experiences, we aim to increase awareness about Balo's type MS in pediatric populations and provide clinical insights into effective management strategies for similar cases in clinical practice.

conclusionsTimely detection of atypical demyelinating lesions together with immediate treatment intervention plays a crucial role in pediatric Baló-type MS. These cases demonstrate the essential role of advanced imaging and immunological testing in precise diagnosis while showcasing successful treatment approaches through corticosteroids and second-line immunotherapies, which improve patient outcomes in this atypical MS variant.

Indexed as

Baló’s concentric sclerosiscerebral MRIMR spectroscopypediatric multiple sclerosistumefactive demyelinating lesion

Identifiers

PMID40426809
PMCPMC12109845

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