Pattern of Behcet's Disease in Sohag Governorate
Abo Al-Fadl, E., Radwan, A., Ali, M. (2019). Pattern of Behcet's Disease in Sohag Governorate. EKB Journal Management System, 23(2), 6-17. doi: 10.21608/smj.2019.45687
Esam Mohammed Abo Al-Fadl; Ahmed R Radwan; Manar Gamal Ali. "Pattern of Behcet's Disease in Sohag Governorate". EKB Journal Management System, 23, 2, 2019, 6-17. doi: 10.21608/smj.2019.45687
Abo Al-Fadl, E., Radwan, A., Ali, M. (2019). 'Pattern of Behcet's Disease in Sohag Governorate', EKB Journal Management System, 23(2), pp. 6-17. doi: 10.21608/smj.2019.45687
Abo Al-Fadl, E., Radwan, A., Ali, M. Pattern of Behcet's Disease in Sohag Governorate. EKB Journal Management System, 2019; 23(2): 6-17. doi: 10.21608/smj.2019.45687

Pattern of Behcet's Disease in Sohag Governorate

Sohag Medical Journal
Article 8, Volume 23, Issue 2, April 2019, Page 6-17  XML PDF (200.45 K)
Document Type: Original Article
DOI: 10.21608/smj.2019.45687
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Authors
Esam Mohammed Abo Al-Fadl1; Ahmed R Radwanorcid 2; Manar Gamal Ali3
1Department of Rheumatology, Rehabilitation and Physical medicine,Faculty of Medicine- Sohag University.
2Department of Rheumatology and Rehabilitation, Faculty of Medicine, Sohag University.
3Department of physical Medicine, Rheumatology and rehabilitation, Faculty of Medicine, Sohag University.
Abstract
Behçet’s disease (BD) is a chronic inflammatory disease with multisystem involvement. It presents with remission and exacerbation. The aim of our study was to study the pattern of Behcet's disease among patients attending the Rheumatology and Rehabilitation Department, SohagUniversity. Conclusion: Behcet's disease starts frequently around the beginning of the third decade and has a male predominance (70%). The age at diagnosis of Behcet's disease ranged from 19-59 years, with a mean of around 28.8 years. Most of the cases in our study were married (73.3%). It was found that the most common first manifestation in our study group was oral ulcers, followed by ocular manifestations, then CNS manifestations, articular or vascular manifestations and lastly genital ulcer or skin manifestations.
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References
  1. Behçet H. Überrezidivieren deAphthose, durchein Virus verursachteGeshwüre am Munde, am Auge und an den Genitalien. Dermatol Wochenschr. 1937;105:1152–1157.
  2. Yazisiz V. Similarities and differences between Behcet's disease and Crohn's disease. World J Gastrointest Pathophysio l2014;5(3):228-38.
  3. Davatchi F, Shahram F, Chams-Davatchi C, Shams H, Nadji A, Akhlaghi M, et al. Behcet's disease: from East to West. Clin Rheumatol. 2010 Aug;29 (8):823-33
  4. Yazici, Y., S. Yurdakul and H. Yazici. Behcet's syndrome. CurrRheumatol Rep 2010;12(6): 429-35
  5. Ambrose, N. L. and D. O. Haskard. Differential diagnosis and management of Behcet syndrome. Nat Rev Rheumatol2013;9(2): 79-89.
  6. Tugal-TutkunI, Gupta V and Cunningham ET. Differential diagnosis of Behcet uveitis. Ocul Immunol Inflamm2013;21(5):337-50.
  7. Ben Ghorbel, I., R. Ennaifer, M. Lamloum, M. Khanfir, M. Miled, and M. H. Houman. Budd-Chiari syndrome associated with Behcet's disease."  Gastroenterol Clin Biol 2008;32(3):316-20.
  8. Yilmaz S, Karadag O, Yazisiz V, Altun B, Gezer M, Karaman M, Cinar M, Erdem H, Pay S, Dinc A. Systemic involvements and preferred treatments in a large cohort of Behcet's disease. Rheumatol Int 2013; 33(12):3025-30.
  9. Mendes D, Correia M, Barbedo M, Vaio T, Mota M, Gonçalves O, Valente J. Behçet’s disease - a contemporary review. J Autoimmun. 2009;32(3-4):178-88.
  10. Deuter CM, Kِtter I, Wallace GR, Murray PI, Stübiger N, Zierhut M. Behçet’s disease: ocular effects and treatment. Prog Retin Eye Res. 2008;27(1):111-36.
  11. Tugal-Tutkun I. Behçet’s uveitis. Middle East Afr J Ophthalmol. 2009;16(4):219-24.
  12. Uva L, Miguel D, Pinheiro C, Filipe P, Freitas JP. Mucocutaneous manifestations of Behçet's disease. Acta Reumatol Port. 2013;38(2):77-90
  13. Coutinho I, Diana Silva, Isabel Ferreira, Bruno Grima. Behçet disease: our experience. Rev Bras Oftalmol. 2017; 76 (4): 210-12.
  14. Ishido T, Horita N, Takeuchi M, Kawagoe T, Shibuya E, Yamane T, Hayashi T, Meguro A, Ishido M, Minegishi K, et al. Clinical manifestations of Behçet’s disease depending on sex and age: results from Japanese nationwide registration. Rheumatology, 2017(Nov); 56 (11): 1918–27.
  15. Pipitone N, Boiardi L, Olivieri I, Cantini F, Salvi F, Malatesta R, La Corte R, Triolo G, Ferrante A, Filippini D, Paolazzi G, Sarzi-Puttini P, Restuccia G, Salvarani C. Clinical manifestations of Behçet’s disease in 137 Italian patients: Results of a multicenter study. Clinical and Experimental Rheumatology, 2004; 22 (Suppl. 36): S46-S51.
  16. Oliveira AC, Buosi AL, Dutra LA, de Souza AW. Behçet disease: clinical  features and management in a Brazilian tertiary hospital. J Clin Rheumatol. 2011 Dec;17(8):416-20.
  17. El-Najjar AR, Abou El-Soud AM, Amara HA, Diabb MA. Clinical characteristics and disease activity of Behçet’s disease patients in
    Zagazig, Egypt. The Egyptian Rheumatologist. 2015;37(4):191-6.
  18. Esatoglu SN, Kutlubay Z, Ucar D, Hatemi I, Uygunoglu U, Siva A, Hatemi
    G. Behçet’s syndrome: providing integrated care. Journal of  Multidisciplinary Healthcare. 2017;2017(10):309-19.
  19. Davatchi F, Shahram F, Chams-Davatchi C, Shams H, Nadji A, Akhlaghi M, Faezi T, Ghodsi Z, Farida A, Ashofteh F, Sadeghi Abdollahi B. Behcet's disease: from East to West. Clin Rheumatol. 2010 Aug;29 (8):823-33.
  20. Al Ghafri A, Al Wahshi H. Demographic features and clinical aspects of Behçet’s disease in Omani patients. Rheumatology Practice and Research, 2018.
  21. Zouboulis CC, Vaiopoulos G, Marcomichelakis N. Onset signs, clinical
    course, prognosis, treatment, and outcome of adult patients with Adamantiades - Behçet’s disease in Greece. Clin Exp Rheumatol 2003; 21: S19-26.
  22. Hum M, Muhammad N. Mahmood, Vivian Huang, Marlene Dytoc. Pancreatitis is a rare manifestation of Behçet disease.2017;3(6):470-3.
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