Behçet’s syndrome-like features revealing myelodysplastic syndrome with TP53 mutation: a case report
mutations, findings highly indicative of MDS. After confirmation of diagnosis and prognostic assessment, the patient ultimately underwent successful allogeneic stem cell transplantation. This case highlights the importance of comprehensive genomic profiling in diagnosing, risk-stratifying, and managing patients with rare hematological entities presenting with autoinflammatory phenomena.
Authors
- Sonja Pavlović (ORCID: https://orcid.org/0000-0002-2915-1641)
- Jelena Ljubičić (ORCID: https://orcid.org/0009-0001-6471-2037)
- Andrej Pešić (ORCID: https://orcid.org/0000-0002-6246-0198)
- Marina Andjelković (ORCID: https://orcid.org/0000-0002-4086-6197)
- Kristel Klaassen (ORCID: https://orcid.org/0000-0002-3077-6091)
- Milena Todorovic Balint
- Maja Stojanovic
Institutions
- University of Belgrade (RS)
- Institute of Molecular Genetics (RU)
- University Clinical Centre (PL)
Publication Details
- Journal
- Frontiers in Immunology
- Published
- 2026-04-01
- DOI
- https://doi.org/10.3389/fimmu.2026.1803414
- Primary Topic
- Ocular Diseases and Behçet’s Syndrome
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Ministarstvo Prosvete, Nauke i Tehnološkog Razvoja
- NIH Clinical Center