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Behcet’s Disease in an Adult Male From Nepal: A Case Report
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  • Madan Basnet,
  • Abisha Phudong,
  • Kamal Gautam,
  • Bishnu Pathak,
  • Suman Gaire,
  • Narayan Bohara,
  • Ayushi Srivastava
Madan Basnet
Tribhuvan University Teaching Hospital

Corresponding Author:[email protected]

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Abisha Phudong
Nepalese Army Institute of Health Sciences
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Kamal Gautam
Patan Academy of Health Sciences
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Bishnu Pathak
Shree Birendra Hospital
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Suman Gaire
Palpa hospital
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Narayan Bohara
Oxford University Clinical Research Unit
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Ayushi Srivastava
Norvic International Hospital
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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
Oct 2021Published in Clinical Case Reports volume 9 issue 10. 10.1002/ccr3.4912