Валеология: Здоровье, Болезнь, Выздоровление. 2019; : 249-254
КЛИНИЧЕСКИЙ СЛУЧАЙ БИЛАТЕРАЛЬНОГО ПАНУВЕИТА У ПАЦИЕНТА ЖЕНСКОГО ПОЛА С БОЛЕЗНЬЮ БЕХЧЕТА
Аннотация
Болезнь Бехчета – редкое аутоиммунное заболевание, поражающее различные органы, в том числе и глаза. Частота поражений глаз при этом заболевании достигает 50-70 % и в среднем развивается на 2-й – 3-й год заболевания и приводит к инвалидизации в трудоспособном возрасте. Согласно данным ряда авторов, более тяжелое поражение глаз характерно для лиц мужского пола. Нами представлен клинический случай развития тяжелого поражения глаз у пациента женского пола с болезнью Бехчета в Казахстане.
Список литературы
1. Nobuyoshi Kitaichi, Akiko Miyazaki, Miles R. Stanford, Hormoz Chams, Daiju Iwata, Shigeaki Ohno Ocular features of Behcet’s disease: An international collaborative study. Br J Ophthalmol 2007; 91 : 1579–1582.
2. Sakane T., Takeno M., Suzuki N, et al. Behcet’s disease. N Engl J Med 1999; 341 : 1284–91.
3. Akiyama K., Numaga J., Yoshida A., et al. Statistical analysis of endogenous uveitis at Tokyo University Hospital (1998–2000). Jpn J Ophthalmol 2006;50:69–71.
4. Hamdan A., Mansour W., Uthman I., et al. Behcet’s disease in Lebanon: clinical profile, severity and two-decade comparison. Clin Rheumatol 2006 ;25 : 364–7.
5. Krause I., Mader R., Sulkes J., et al. Behcet’s disease in Israel: the influence of ethnic origin on disease expression and severity. J Rheumatol 2001; 28 : 1033–6.
6. Kural-Seyahi E., Fresko I., Seyahi N., et al. The long-term mortality and morbidity of Behcet syndrome: a 2-decade outcome survey of 387 patients followed at a dedicated center. Medicine (Baltimore) 2003; 82 : 60–76.
7. Алекберова З. С. Болезнь Бехчета (лекция) / З. С. Алекберова / Федеральное государственное бюджетное учреждение «Научно-исследовательский институт ревматологии» РАМН. – Москва, 2012
8. Tugal-Tutkun J., Onal S., Yaycioglu R. et al. Uveitis in Behcet’s disease: analysis of 880 patients. Am J Ophthalmol 2004; 138 : 373-80.
9. Tursen U., Gurler A. & Boyvat A., Evaluation of clinical findings according to sex in 2313 Turkish patients with Behçet’s disease, 2013, Int J Dermatol. Vol.42, No.5, pp.346-351.
10. Tugal-Tutkun I., Urgancioglu M. Childhood-onset uveitis in Behc¸et disease: a descriptive study of 36 cases. Am J Ophthalmol 2003; 136 : 1114–1119.
11. Wechler B., Sable-Fourttaason R., Bodaghi B. et al. Infliximab in refractory uveitis due to Behcet’s disease. Clin Exper Rheum 2004; 22 (Suppl 34) : 14-6.
12. Matsuo T., Itami M., Nakagawa H. The incidence and pathology of conjunctival ulceration in Behcet’s syndrome. Br J Ophthalmol 2002; 86 : 140–143.
13. Tugal-Tutkun I., Onal S., Altan-Yaycioglu R., Kir N. & Urgancioglu M. (2006). Neovascularization of the optic disc in Behзet’s disease. Jpn J Ophthalmol. Vol. 50, No. 3, pp. 256-265.
14. Dursun D., Akova Y., Yicel E. (2004). Myositis and scleritis associated with Behcet’s disease: an atypical presentation. Ocul Immunol Inflamm. 2004 Vol. 12, No. 4, pp. 329-332.
15. Kazokoglu H., Onal S., Tugal-Tutkun I., Mirza E., Akova Y., Ozyazgan Y., Soylu M., Batioglu F. & Apaydin C. (2008). Demographic and clinical features of uveitis in tertiary centers in Turkey. Ophthalmic Epidemiol. Vol. 15, No. 5, pp. 285-293.
16. Prokaeva T., Madanat W., Yermakova N., Alekberova Z. Sex dimorphism of Behзet’s Disease. In: Godeau P., Wechsler B., eds. Behзet’s Disease. Amsterdam: Elsevier Science Publishers, 1993 : 219–221.
17. Zouboulis Ch. C., Djawari D., Kirch W., et al. Adamatiades- Behзet’s Disease in Germany. In: Godeau P., Wechsler B., eds. Behзet’s Disease. Amsterdam: Elsevier. Science Publishers, 1993 : 193–196.
18. Yazycy H., Tuzun Y., Pazarlı H., et al. Influence of age of onset and patient’s sex on the prevalence and severity of manifestations of Behзet’s syndrome. Ann Rheum Dis 1984; 43: 783–789.
Valeology: Health - Illnes - recovery. 2019; : 249-254
THE CLINICAL CASE OF BILATERAL PANUVEITIS IN A FEMALE PATIENT WITH BEHCHET`S DISEASE
Abstract
Behcet’s disease is a rare autoimmune disease that affects various organs, including the eyes. The frequency of eye damage in this disease reaches 50-70 % and an average develops on 2-3 years of the disease and leads to disability in working age. According to data of a number of authors, severe eye lesions are more specific to male patients. We present the clinical case of serious eye lesions in a female patient with Behcet’s disease in Kazakhstan.
References
1. Nobuyoshi Kitaichi, Akiko Miyazaki, Miles R. Stanford, Hormoz Chams, Daiju Iwata, Shigeaki Ohno Ocular features of Behcet’s disease: An international collaborative study. Br J Ophthalmol 2007; 91 : 1579–1582.
2. Sakane T., Takeno M., Suzuki N, et al. Behcet’s disease. N Engl J Med 1999; 341 : 1284–91.
3. Akiyama K., Numaga J., Yoshida A., et al. Statistical analysis of endogenous uveitis at Tokyo University Hospital (1998–2000). Jpn J Ophthalmol 2006;50:69–71.
4. Hamdan A., Mansour W., Uthman I., et al. Behcet’s disease in Lebanon: clinical profile, severity and two-decade comparison. Clin Rheumatol 2006 ;25 : 364–7.
5. Krause I., Mader R., Sulkes J., et al. Behcet’s disease in Israel: the influence of ethnic origin on disease expression and severity. J Rheumatol 2001; 28 : 1033–6.
6. Kural-Seyahi E., Fresko I., Seyahi N., et al. The long-term mortality and morbidity of Behcet syndrome: a 2-decade outcome survey of 387 patients followed at a dedicated center. Medicine (Baltimore) 2003; 82 : 60–76.
7. Alekberova Z. S. Bolezn' Bekhcheta (lektsiya) / Z. S. Alekberova / Federal'noe gosudarstvennoe byudzhetnoe uchrezhdenie «Nauchno-issledovatel'skii institut revmatologii» RAMN. – Moskva, 2012
8. Tugal-Tutkun J., Onal S., Yaycioglu R. et al. Uveitis in Behcet’s disease: analysis of 880 patients. Am J Ophthalmol 2004; 138 : 373-80.
9. Tursen U., Gurler A. & Boyvat A., Evaluation of clinical findings according to sex in 2313 Turkish patients with Behçet’s disease, 2013, Int J Dermatol. Vol.42, No.5, pp.346-351.
10. Tugal-Tutkun I., Urgancioglu M. Childhood-onset uveitis in Behc¸et disease: a descriptive study of 36 cases. Am J Ophthalmol 2003; 136 : 1114–1119.
11. Wechler B., Sable-Fourttaason R., Bodaghi B. et al. Infliximab in refractory uveitis due to Behcet’s disease. Clin Exper Rheum 2004; 22 (Suppl 34) : 14-6.
12. Matsuo T., Itami M., Nakagawa H. The incidence and pathology of conjunctival ulceration in Behcet’s syndrome. Br J Ophthalmol 2002; 86 : 140–143.
13. Tugal-Tutkun I., Onal S., Altan-Yaycioglu R., Kir N. & Urgancioglu M. (2006). Neovascularization of the optic disc in Behzet’s disease. Jpn J Ophthalmol. Vol. 50, No. 3, pp. 256-265.
14. Dursun D., Akova Y., Yicel E. (2004). Myositis and scleritis associated with Behcet’s disease: an atypical presentation. Ocul Immunol Inflamm. 2004 Vol. 12, No. 4, pp. 329-332.
15. Kazokoglu H., Onal S., Tugal-Tutkun I., Mirza E., Akova Y., Ozyazgan Y., Soylu M., Batioglu F. & Apaydin C. (2008). Demographic and clinical features of uveitis in tertiary centers in Turkey. Ophthalmic Epidemiol. Vol. 15, No. 5, pp. 285-293.
16. Prokaeva T., Madanat W., Yermakova N., Alekberova Z. Sex dimorphism of Behzet’s Disease. In: Godeau P., Wechsler B., eds. Behzet’s Disease. Amsterdam: Elsevier Science Publishers, 1993 : 219–221.
17. Zouboulis Ch. C., Djawari D., Kirch W., et al. Adamatiades- Behzet’s Disease in Germany. In: Godeau P., Wechsler B., eds. Behzet’s Disease. Amsterdam: Elsevier. Science Publishers, 1993 : 193–196.
18. Yazycy H., Tuzun Y., Pazarlı H., et al. Influence of age of onset and patient’s sex on the prevalence and severity of manifestations of Behzet’s syndrome. Ann Rheum Dis 1984; 43: 783–789.
