International consensus recommendations for the diagnosis and treatment of Rasmussen syndrome: A modified Delphi procedure

Rasmussen syndrome (RS) includes a well-described constellation of refractory focal seizures, often including epilepsia partialis continua, hemiplegia with progressive unilateral cortical atrophy, and cognitive/language decline. However, the precise early pathogenesis and reliable biomarkers remain elusive. In addition, we lack operational management guidelines, including diagnostic evaluation, disease-monitoring assessments, and medical and surgical treatment approaches. We aimed to create an expert consensus statement to guide and standardize the treatment of RS, with the goal of providing recommendations applicable to a global population. An expert panel was convened to complete three rounds of a modified Delphi procedure given the lack of high-level evidence, with a focus on workup to exclude mimicking diagnoses, disease-activity metrics, and treatment. Consensus was defined as ≥75% of responses being agree/strongly agree in either two subsequent rounds or in the third and final round. A total of 122 of 143 statements met consensus. Proposed diagnostic evaluation in patients with possible RS is outlined, including physical examination, blood/cerebrospinal fluid analyses, neuroimaging, electroencephalography (EEG), and biopsy. Suggested disease-monitoring assessments include neuropsychological testing and serial magnetic resonance imaging (MRI). Intravenous corticosteroids are recommended as first-line, acute immunotherapy for seizure exacerbations and status epilepticus, with or without the addition of intravenous immunoglobulin. Options for maintenance immunotherapy are outlined, with lack of evidence noted for comparing efficacy of these treatments. Hemispheric disconnection remains the most effective seizure treatment, with parameters including age, function, seizure burden, and patient values influencing candidacy for surgery. This consensus statement offers a guideline to standardize management, as well as suggests future directions to further elucidate underlying pathophysiology and target more-effective, better-tolerated treatments.

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Publication Details

Journal
Epilepsia
Published
2026-04-24
DOI
https://doi.org/10.1002/epi.70225
Primary Topic
Epilepsy research and treatment
Type
article
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article

International consensus recommendations for the diagnosis and treatment of Rasmussen syndrome: A modified Delphi procedure

Maria T. Papadopoulou, Coral M. Stredny, Ronny Wickström, Tilman Polster et al.
Epilepsia
Epilepsy research and treatment
article

International consensus recommendations for the diagnosis and treatment of Rasmussen syndrome: A modified Delphi procedure

Maria T. Papadopoulou, Coral M. Stredny, Ronny Wickström, Tilman Polster, Marios Kaliakatsos, Claude Steriade, Stuart Tomko, Suresh Pujar, Bo Zhang, Christopher Cortina, International Rasmussen Syndrome Consensus Group
article en

Abstract

Rasmussen syndrome (RS) includes a well-described constellation of refractory focal seizures, often including epilepsia partialis continua, hemiplegia with progressive unilateral cortical atrophy, and cognitive/language decline. However, the precise early pathogenesis and reliable biomarkers remain elusive. In addition, we lack operational management guidelines, including diagnostic evaluation, disease-monitoring assessments, and medical and surgical treatment approaches. We aimed to create an expert consensus statement to guide and standardize the treatment of RS, with the goal of providing recommendations applicable to a global population. An expert panel was convened to complete three rounds of a modified Delphi procedure given the lack of high-level evidence, with a focus on workup to exclude mimicking diagnoses, disease-activity metrics, and treatment. Consensus was defined as ≥75% of responses being agree/strongly agree in either two subsequent rounds or in the third and final round. A total of 122 of 143 statements met consensus. Proposed diagnostic evaluation in patients with possible RS is outlined, including physical examination, blood/cerebrospinal fluid analyses, neuroimaging, electroencephalography (EEG), and biopsy. Suggested disease-monitoring assessments include neuropsychological testing and serial magnetic resonance imaging (MRI). Intravenous corticosteroids are recommended as first-line, acute immunotherapy for seizure exacerbations and status epilepticus, with or without the addition of intravenous immunoglobulin. Options for maintenance immunotherapy are outlined, with lack of evidence noted for comparing efficacy of these treatments. Hemispheric disconnection remains the most effective seizure treatment, with parameters including age, function, seizure burden, and patient values influencing candidacy for surgery. This consensus statement offers a guideline to standardize management, as well as suggests future directions to further elucidate underlying pathophysiology and target more-effective, better-tolerated treatments.

Epilepsia
Boston Children's Hospital (US), St. Louis Children's Hospital (US), Neurosciences Institute (US), Bielefeld University (DE), Great Ormond Street Hospital for Children NHS Foundation Trust (GB), NYU Langone Health (US), Centre de Recherche en Neurosciences de Lyon (FR), Hospices Civils de Lyon (FR), Evangelisches Krankenhaus Bielefeld (DE), Sachs' Children and Youth Hospital (SE), Boston Children's Museum (US), St Göran's Children's Hospital (SE), New York University (US)
Openalex Percentile: Top 7%
Epilepsy research and treatment
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