Lipid Storage Myopathy in Behçet's Disease: A Rare Cause of Elevated Serum Creatine Kinases Levels
Muscular involvement in Behçet’s disease is rare and there are only a few case reports in the literature. The causes of elevated muscle enzymes in a patient with Behcet’s disease are many, including myositis, drug-induced myopathy, metabolic myopathy ...
Sedat Yilmaz +6 more
doaj +1 more source
When to consider an inborn error of immunity: clues for physicians
Abstract The term inborn errors of immunity (IEIs) refers to the rapidly expanding group of genetic disorders causing dysregulation of the immune system. With improved genetic testing in recent years, the number of defined IEIs and their range of phenotypic presentations has grown vastly, with more than 550 IEIs now described.
Meera Thangarajah, Lucinda J. Berglund
wiley +1 more source
Malignant lymphoma associated with Behçet’s disease: A report of 2 cases
Herein we report 2 cases of malignant lymphoma associated with Behçet’s disease. Case 1, a 53-year-old man, was diagnosed as Behçet’s disease at the age of 26 years, and was treated with cyclophosphamide and prednisolone.
Ahmet Deniz Meydan +4 more
doaj +3 more sources
A rare involvement in Behcet's Disease: Carotid artery aneurysm
Behçet's disease is an inflammatory disease characterized by recurrent oral aphthous ulcers and various accompanying systemic pathologies. These additional pathologies include ocular and neurologic disease, genital ulcers, skin lesions, arthritis and ...
Hamit Serdar Başbuğ +3 more
doaj +1 more source
Delphi consensus: First‐line use of biologics and small molecules in hidradenitis suppurativa
This Delphi Consensus study identified upgrade criteria for the use of biologics and small molecules as first‐line therapy in hidradenitis suppurativa (HS). European HS experts evaluated 16 clinical scenarios, voting on eligibility for therapy escalation.
Georgios Nikolakis +54 more
wiley +1 more source
T LYMPHOCYTE SUBGROUPS IN THE PATIENTS WITH ACTIVE AND INACTIVE BEHÇET’S DISEASE
Immunological changes have an important role in the etiopathogenesis of Behçet's disease. Inflammation derived by immunological mechanisms is responsible from the signs and findings of disease.
Refik Ali Sarı +3 more
doaj
Bimekizumab efficacy using IHS4 outcomes in hidradenitis suppurativa: Results from BE HEARD I and II
The majority of bimekizumab‐treated patients shifted from severe to mild and moderate IHS4 stages, and nearly 25% achieved an IHS4 of 0 by Week 48. Bimekizumab led to clinically meaningful improvements across IHS4 outcome measures. These data highlight an opportunity to address the need for effective treatments against draining tunnels.
Thrasyvoulos Tzellos +15 more
wiley +1 more source
Correlation of Otorhinolaryngologic Symptoms with Physical Findings in Behçet’s Disease
Correlation of Otorhinolaryngologic Symptoms with Physical Findings in Behçet’s Disease. Objective: Behçet’s disease is a chronic systemic inflammatory disease of unknown etiology.
A. Meric +5 more
doaj +2 more sources
Brain biopsy to aid diagnosis of neuro-Behçet's disease: Case report and literature review
Central nervous system involvement in Behçet's disease (Neuro-Behçet's disease: NBD) has been reported to present diverse clinical and pathological manifestations.
Hiroki Yamada +3 more
doaj +1 more source
Measuring success in HS treatment from the physician's and the patient's perspective
Integrated clinician (HiSCR, IHS4, IHS4‐55, HS‐IGA) and patient (HiSQOL, DLQI) scores, combined with imaging‐based fibrosis and inflammation assessment, redefine treatment success in hidradenitis suppurativa by aligning treat‐to‐target strategies with both inflammatory control and irreversible structural damage.
Georgios Nikolakis +4 more
wiley +1 more source

