• MIDHUN M NAIR
• Dr. SAI KEERTHANA P C
• RAZEENA ISMAIL
• NADA THESNEEM
• Dr. FATHIMATHU SHADIYA C H

Behçet’s disease (BD) is a rare, chronic inflammatory disorder characterized by recurrent oral and genital ulcers, skin lesions, and eye manifestations. This condition primarily affects young adults. Its exact cause remains unknown, though it is believed to be caused due to autoimmune and genetic factors. This case study presents a 32-year-old female admitted with fever, headaches, recurrent skin and oral ulcers, and eye complications including pseudophakia in the left eye and hemorrhage and detachment in the right. Additionally, she suffered from arthritis and abdominal aortitis. Blood tests showed positive pathergy and negative HLA-B51 antigen. She was diagnosed with Behcet’s and treated with Adalimumab for 6 months, resulting in improved eye inflammation, alongside cyclophosphamide, steroids, and Rituximab. Behcet’s disease presents diagnostic challenges due to its various symptoms, often leading to delays in diagnosis and treatment. Management focuses on symptom relief and prevention of complications.

Behçet’s disease, Pseudophakia, Human Leukocyte -B51 Antigen, Uveitis.

" A CASE STUDY ON BECHET's DISEASE ASSOCIATED WITH CYCLOPHOSPHAMIDE-INDUCED CARDIAC FAILURE", International Journal of Emerging Technologies and Innovative Research (www.jetir.org), ISSN:2349-5162, Vol.11, Issue 3, page no.h199-h202, March-2024, Available :http://www.jetir.org/papers/JETIR2403723.pdf

" A CASE STUDY ON BECHET's DISEASE ASSOCIATED WITH CYCLOPHOSPHAMIDE-INDUCED CARDIAC FAILURE", International Journal of Emerging Technologies and Innovative Research (www.jetir.org | UGC and issn Approved), ISSN:2349-5162, Vol.11, Issue 3, page no. pph199-h202, March-2024, Available at : http://www.jetir.org/papers/JETIR2403723.pdf