Evidence map›Paper›PMID 42516391›Full record

ArticleFrontiers in immunology2026

Two cases of probable Neuro-Behçet syndrome treated with autologous HSCT.

Charlotte Schubert, Lea I Walter, Marina Herwerth, Imke Metz, Jakob Nilsson, Ilijas Jelcic, Patrick Roth, Nicolaus Kröger, Ina Kötter, Christoph Heesen and 2 more

Abstract readCase Reports
In one paragraph

Article in Frontiers in immunology, 2026. 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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0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Charlotte Schubert *Institute of Neuroimmunology and Multiple Sclerosis (INIMS) and Department of Neurology, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
Lea I Walter *Department of Neurology, University Hospital Zurich and University of Zurich, Zurich, Switzerland.
Marina HerwerthDepartment of Neurology, University Hospital Zurich and University of Zurich, Zurich, Switzerland.
Imke MetzInstitute of Neuropathology, University Medical Centre Göttingen, Göttingen, Germany.
Jakob NilssonDepartment of Immunology, University Hospital Zurich, Zurich, Switzerland.
Ilijas JelcicDepartment of Neurology, University Hospital Zurich and University of Zurich, Zurich, Switzerland.
Patrick RothDepartment of Neurology, University Hospital Zurich and University of Zurich, Zurich, Switzerland.
Nicolaus KrögerDepartment of Stem Cell Transplantation, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
Ina KötterDivision of Rheumatology and Systemic Inflammatory Diseases, III. Department of Medicine, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
Christoph HeesenInstitute of Neuroimmunology and Multiple Sclerosis (INIMS) and Department of Neurology, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
Vivien Häußler *Institute of Neuroimmunology and Multiple Sclerosis (INIMS) and Department of Neurology, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.
Veronika Kana *Department of Neurology, University Hospital Zurich and University of Zurich, Zurich, Switzerland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neuro-Behçet syndrome (NBS) is a rare but detrimental neurological manifestation of the Behçet syndrome (BS) - a chronic multisystemic inflammatory disease. NBS is frequently associated with brainstem and spinal cord lesions, often resulting in substantial neurological disability. Atypical clinical presentations can pose significant challenges for diagnosis and treatment of NBS. Here, we report the clinical course, treatment strategies and responses of two cases with probable NBS. Both cases presented with longitudinally extensive transverse myelitis and brainstem lesions and experienced recurrent relapses as well as disease progression resistant to multiple immunotherapies. Autologous hematopoietic stem cell transplantation (aHSCT) was without beneficial effect on the disease course in both cases. In summary, NBS or probable NBS should be considered in patients with myelitis and brainstem involvement with limited treatment response. These cases illustrate diagnostic challenges and limitations of current diagnostic criteria, while also underscoring the heterogeneity of disease presentation. Immune reset by aHSCT failed to confer clinical benefit as a rescue therapy in these two patients. Further studies are required to optimize therapeutic strategies for NBS.

Indexed as

Behcet SyndromeHematopoietic Stem Cell TransplantationAdultHumansMagnetic Resonance ImagingMaleMiddle AgedTransplantation, AutologousTreatment OutcomeaHSCTBehçet syndromecase reportmyelitisstem cell therapy

Identifiers

PMID42516391
PMCPMC13403935

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