ReviewClinical and experimental immunology2009
Clinical Immunology Review Series: an approach to the patient with recurrent orogenital ulceration, including Behçet's syndrome.
Review in Clinical and experimental immunology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.
What it found
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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.
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Who cites it
21 citing papers in PubMed.
- Pemphigus Vulgaris Mimicking Behçet's Syndrome With Oral and Vulvar Ulcers: A Case Report.Cureus · 2026Article
- Recurrent reactive non-sexually related acute genital ulcers: a risk factor for Behcet's disease?Acta bio-medica : Atenei Parmensis · 2022Article
- Article
- Trends in Hospitalization and Inpatient Outcomes of Behçet's Disease: A Nationwide Inpatient Sample Study.Cureus · 2020Article
- Vascular suture line wrapping for Aortoiliac anastomoses following open surgical repair of Infrarenal Behçet's Aortoiliac aneurysms.Orphanet journal of rare diseases · 2019Article
- Cutaneous Polyarteritis Nodosa Presenting Atypically with Severe Pharyngeal Ulceration.Case reports in rheumatology · 2019Article
- Clinical Significance of Serum Bilirubin in Behçet's Disease.Journal of translational internal medicine · 2018Article
- The influence of oral health and psycho-social well-being on clinical outcomes in Behçet's disease.Rheumatology international · 2018Article
- Article
- Genital ulcer severity score and genital health quality of life in Behçet's disease.Orphanet journal of rare diseases · 2015Article
- Genital aphthosis in Behçet's disease: is it associated with less eye involvement?Rheumatology international · 2014Article
- Association of Rho-kinase 1 (ROCK1) gene polymorphisms with Behçet's disease.Molecular diagnosis & therapy · 2014Article
- Update on the therapy of Behçet disease.Therapeutic advances in chronic disease · 2014Review
- Recurrent aphthous stomatitis.Dental clinics of North America · 2014Review
- A young girl with refractory intestinal Behçet's disease: a case report and review of literatures on pediatric cases who received an anti-tumor necrosis factor agent.Rheumatology international · 2013Review
- In pursuit of excellence: an integrated care pathway for C1 inhibitor deficiency.Clinical and experimental immunology · 2013Article
- Fournier's Gangrene Associated with Local Cutaneous HPV Lesions in a Previously Healthy Girl.Case reports in pediatrics · 2013Article
- Case 2: A 14-year-old girl with oral and genital ulcers.Paediatrics & child health · 2013Article
- Comparing the Effect of Phenytoin Syrup and Triamcinolone Acetonide Ointment on Aphthous Ulcers in Patients with Behcet's Syndrome.Iranian Red Crescent medical journal · 2012Article
- Clinical and Pathological Manifestations with Differential Diagnosis in Behçet's Disease.Pathology research international · 2012Article
Corrections and comments
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Authors and funding
1 author.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Patients presenting with recurrent orogenital ulcers may have complex aphthosis, Behçet's disease, secondary complex aphthosis (e.g. Reiter's syndrome, Crohn's disease, cyclical neutropenia) or non-aphthous disease (including bullous disorders, erythema multiforme, erosive lichen planus). Behçet's syndrome is a multi-system vasculitis of unknown aetiology for which there is no diagnostic test. Diagnosis is based on agreed clinical criteria that require recurrent oral ulcers and two of the following: recurrent genital ulcers, ocular inflammation, defined skin lesions and pathergy. The condition can present with a variety of symptoms, hence a high index of suspicion is necessary. The most common presentation is with recurrent mouth ulcers, often with genital ulcers; however, it may take some years before diagnostic criteria are met. All patients with idiopathic orogenital ulcers should be kept under review, with periodic focused assessment to detect evolution into Behçet's disease. There is often a delay of several years between patients fulfilling diagnostic criteria and a diagnosis being made, which may contribute to the morbidity of this condition. Despite considerable research effort, the aetiology and pathogenesis of this condition remains enigmatic.
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.