Literature DB >> 8647999

Prognosis and clinical relevance of recurrent oral ulceration in Behçet's disease.

D Bang1, W Hur, E S Lee, S Lee.   

Abstract

There is no way of predicting whether a patient with recurrent oral ulcerations (ROU) will develop Behçet's disease (BD). In the absence of a valid laboratory test to exclude BD, such oral ulcerations result in a diagnostic problem when they occur as the sole and earliest manifestation of disease. We assessed the prognosis of ROU by performing prospective evaluations of 67 patients who had only a history of ROU and were registered at the Behçet's Disease Specialty Clinic at Severance Hospital of Yonsei University, Seoul, Korea. Thirty-five patients (52.2%) developed overt manifestations of BD at an average of 7.7 years after the onset of ROU. The frequency of recurrence was 9.8 times per year in progressive cases. From these results, it appears that highly recurrent ROU is a warning signal for BD. Careful examinations of patients, including their minor symptoms, additional laboratory tests, and regular follow-ups by physicians are required for proper diagnosis.

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Year:  1995        PMID: 8647999     DOI: 10.1111/j.1346-8138.1995.tb03947.x

Source DB:  PubMed          Journal:  J Dermatol        ISSN: 0385-2407            Impact factor:   4.005


  7 in total

Review 1.  Clinical Immunology Review Series: an approach to the patient with recurrent orogenital ulceration, including Behçet's syndrome.

Authors:  M T Keogan
Journal:  Clin Exp Immunol       Date:  2008-12-11       Impact factor: 4.330

Review 2.  Urban legends: recurrent aphthous stomatitis.

Authors:  L Baccaglini; R V Lalla; A J Bruce; J C Sartori-Valinotti; M C Latortue; M Carrozzo; R S Rogers
Journal:  Oral Dis       Date:  2011-08-04       Impact factor: 3.511

Review 3.  Sex Differences in Pediatric Rheumatology.

Authors:  Marco Cattalini; Martina Soliani; Maria Costanza Caparello; Rolando Cimaz
Journal:  Clin Rev Allergy Immunol       Date:  2019-06       Impact factor: 8.667

4.  [Extraocular manifestations of Behcet's disease].

Authors:  I Kötter; T Xenitidis; G Fierlbeck; S Schanz; A Melms; M Horger; U Ernemann; C Deuter
Journal:  Ophthalmologe       Date:  2012-06       Impact factor: 1.059

5.  Genetic variations of IL-12B, IL-12Rβ1, IL-12Rβ2 in Behcet's disease and VKH syndrome.

Authors:  Xinyu Li; Lin Bai; Jing Fang; Shengping Hou; Qingyun Zhou; Hongsong Yu; Aize Kijlstra; Peizeng Yang
Journal:  PLoS One       Date:  2014-05-23       Impact factor: 3.240

Review 6.  Behçet's disease in children, an overview.

Authors:  Isabelle Koné-Paut
Journal:  Pediatr Rheumatol Online J       Date:  2016-02-18       Impact factor: 3.054

7.  A 25-Year-Old Male with Orogenital Ulcers, Rash, and Difficulty Swallowing.

Authors:  Lauren N Ko; Allireza Alloo; William M Lin; Mai P Hoang; Daniela Kroshinsky
Journal:  Dermatopathology (Basel)       Date:  2017-11-08
  7 in total

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