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Published on: April 23, 2021
Delirium as presenting symptom of neuro-Behcet's disease
Rana Alnasser Alsukhni1, Mohamed Sourat Ghoubari2, Yasmin Aboras1
1Division of Neurology, Department of Internal Medicine, Aleppo University Hospital, Aleppo, Syria.
Insights
Behcet
Area of Science:
- Neurology
- Rheumatology
- Vascular Medicine
Background:
- Behcet's disease is a multisystemic inflammatory disorder characterized by thrombosis and vasculitis.
- Neurological manifestations, though less common, can be the initial presentation, prompting medical attention.
Observation:
- A 30-year-old female presented with acute neurological symptoms including severe headaches and confusion.
- Brain MRI revealed bilateral thalamic lesions with hemorrhage, alongside a history of recurrent oral ulcers, miscarriages, and deep venous thrombosis.
Findings:
- Differential diagnoses were excluded, leading to the establishment of Behcet's disease diagnosis.
- The case highlights neurological involvement as a presenting feature of Behcet's disease.
Implications:
- Behcet's disease should be considered in patients with unexplained neurological and systemic symptoms, particularly in endemic regions.
- Timely diagnosis and treatment are crucial, even in critical cases where alternative diagnoses are not apparent.
Objectives:
Behcet's disease is a multisystemic disorder. Most of its clinical manifestations are due to thrombosis or vasculitis. There is a predominance of mucocutaneous and ocular lesions; neurological manifestations are minority. However, this could be the first problem that leads a patient to seek medical help.
Methods:
We report a 30-year-old female with rapidly progressive headaches and confusion. Brain magnetic resonance imaging showed bilateral thalamic T2 hyperintense lesions and hemorrhage. Directed inquiry revealed recurrent oral ulcers and three miscarriages. During hospitalization, the patient developed a deep venous thrombosis.
Results:
After exclusion of other differential diagnoses, the diagnosis of Behcet's disease was established.
Conclusion:
Behcet's disease is a protean disease. Hence it should be in mind in patients with otherwise unexplained signs and symptoms, especially in endemic countries, and treatment decision should not be witheld in critical cases if no alternative diagnosis is plausible.
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