Journals / SSK Tepecik Eğitim Hastanesi Dergisi / 2003 / Cilt: 13 - Sayı: 3

Behçet disease and venous thromboemboli in childhood

Çocukluk çağında Behçet hastalığı ve venöz tromboemboli

Pages
177–180
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

The case is presented because of the rarity of Behçet's disease and also its very rare complication, venous thrombosis, in childhood.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Behçet's disease is a chronic, inflammatory, generalized vasculitis that involves many organs such as skin, eyes and nervous system.
📊
Key Findings & Data:Clinical diagnosis could be made on the basis of the criteria established by the International Behcet's Disease Study Group.
💡
Conclusion & Impact:The case is presented because of the rarity of Behçet's disease and also its very rare complication, venous thrombosis, in childhood.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Erkek · Çocuk · Tromboembolizim

Abstract

Behçet's disease is a chronic, inflammatory, generalized vasculitis that involves many organs such as skin, eyes and nervous system. Clinical diagnosis could be made on the basis of the criteria established by the International Behcet's Disease Study Group. Twelve-years-old male patient was admitted to our hospital with the complaints of swelling and erythema of left ankle extending towards the left knee joint and oral aphthous lesions. Physical examination revealed multiple oral aphthous lesions, genital scar due to prior ulceration, swelling of left ankle and bilateral erythema nodosum like lesions on lower extremities. Venous doppler study of the left lower extremity showed left popliteal deep vein thrombosis. The case is presented because of the rarity of Behçet's disease and also its very rare complication, venous thrombosis, in childhood.

Özet

Behçet Hastalığı (BH), deri, göz , eklem, sinir sistemi gibi bir çok sistemi tutabilen, kronik, inflamatuar, jeneralize bir vaskülit tipidir. Klinik tanı, Uluslararası Behçet Hastalığı Çalışma Grubu'nun belirlediği kriterlere dayanılarak konulabilmektedir. 12 yaşında erkek olgu, l aydır sol ayak bileğinde kızarıklık, şişlik, bu şişliğin zaman zaman sol diz bölgesine kadar ilerlemesi ve oral aftöz lezyonlar yakınmaları ile başvurdu. Fizik bakıda çok sayıda oral aftöz lezyonlar, perianal bölgede geçirilmiş genital ülsere bağlı skar, sol ayak bileğinde şişlik, bilateral alt ekstremitelerde eritema nodozum benzeri döküntüler saptandı. Sol alt ekstremite venöz doppler USG incelemesinde, sol popliteal derin ven trombozu izlendi. Olgu, çocukluk çağında nadir görülen Behçet Hastalığı'nın, çok nadir olarak tromboz komplikasyonu ile birlikte seyretmesi nedeni ile sunulmuştur.

🔖

Cite This Article

SÜTÇÜOĞLU, S., AKDUMAN, İ., BAKİLER, A. R., SALAR, K., TELLİOĞLU, M., SÖZEN, G., ÖZHAN, B. (2003). Behçet disease and venous thromboemboli in childhood. SSK Tepecik Eğitim Hastanesi Dergisi, Cilt: 13 - Sayı: 3, 177–180. https://ajindex.com/articles/312860

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (15)

  1. International Study Group for Behcet's Disease: Criteria for diagnosis of Behcet's Disease. Lancet 1990;27: 197-217
  2. Dilsen N. History and development of Behcet's disease. Rev Rheum Eng 1996;63:512
  3. Gedalia A. Behçet Disease. In: Behrman RE, Kliegman RM, Jenson HB, eds. Nelson Textbook of Pediatrics. 17th ed. Philadelphia: WB Saunders Co, 2004:819-20
  4. Koç Y, Güllü I, Akpek G, Akpolat T, Kansu E, Kiraz S. Vascular involvement in Behcet's disease. J Rheumatol 1992;19:402-10
  5. Kone-Paut I, Yurdakul S, Bahabri SA, et al. Clinical features of Behçet's disease in children: An international collaborative study of 86 cases. J Pediatr 1998;132:721
  6. Mammo L, Al-Dalaan A, Bahabri SS, Saour JN. Association of factor V Leiden with Behçet's Disease. J Rheumatol 1997;24:2196-8
  7. Oner AF, Gurgey A, Gürler A, Mesci L. Factor V Leiden mutation in patients with Behçet's disease. J Rhematol 1998;25:496-8
  8. Krause I, Uziel Y, Guedj D, et al. Mode of presentation and multisystem involvement in Behçet's disease: The influence of sex and age of disease onset. J Rheumatol 1998;25:1566-9
  9. Petty RE, Cassidy JT. Behçet's Disease and other vasculitides. In: Cassidy JT, Petty RE, eds. Textbook of pediatric rheumatology. 4th ed. Philadelphia: WB Saunders Co, 2001:629-33
  10. Chaloupka K, Baglivo E, Hofer M, Chizzolini C, Delavelle J, Rossillion B, et al. Cerebral sinus thrombosis in Behçet disease: Case report and review of the literature. Klin Monatsbl Augenheilkd 2003; 220.186-8
  11. Yazici H, Yurdakul S, Hamuryudan V. Behçet disease. Curr Opin Rheumatol 2001;13:18-22
  12. Gurgey A, Balta G, Boyvat A. Factor V Leiden mutation and PAI-I gene 46/56 genotype in thrombotic patients with Behçet's disease. Blood Coagul Fibrinclysis 2003;14:121-4
  13. Aschka I, Aumann M, Bergmann F. Prevalance of Factor V Leiden in children with thromboembolism. EurJ Pediatr 1996;155:1009-14
  14. Krause I, Uziel Y, Guedj D et al. Childhood Behçet's disease: Clinical features and comparison with adult onset disease. Rheumatology 1999;38:457-62
  15. Shimizu T, Erhlich GE, Inaba G. Behçet's disease (Behçet's syndrome). Semin Arthritis Rheum 1979; 8:223.