Behcet’s Disease in an Adult Male From Nepal: A Case Report
- Madan Basnet,
- Abisha Phudong,
- Kamal Gautam,
- Bishnu Pathak,
- Suman Gaire,
- Narayan Bohara,
- Ayushi Srivastava
Abisha Phudong
Nepalese Army Institute of Health Sciences
Author ProfileAbstract
Behcet's Disease is a rare systemic vasculitis characterized by
recurrent episodes of acute inflammation affecting blood vessels of all
sizes. Symptoms include orogenital apthosis, cutaneous skin lesions, and
uveitis. We present the case of a 38-year-old Nepalese man with Behcet's
Disease. In Nepal, Behcet's Disease may still be under-reported.31 Jul 2021Submitted to Clinical Case Reports 31 Jul 2021Submission Checks Completed
31 Jul 2021Assigned to Editor
06 Aug 2021Reviewer(s) Assigned
09 Aug 2021Review(s) Completed, Editorial Evaluation Pending
15 Aug 2021Editorial Decision: Revise Minor
15 Sep 20211st Revision Received
16 Sep 2021Submission Checks Completed
16 Sep 2021Assigned to Editor
16 Sep 2021Review(s) Completed, Editorial Evaluation Pending
22 Sep 2021Editorial Decision: Accept