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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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Abstract

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.

Peer review status:Published

31 Jul 2021Submitted to Clinical Case Reports
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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