Publication:
Behcet’s Disease with Absent HLA Serotyping and Pathergy Test

creativeworkseries.issn1812-2027
dc.contributor.authorRanabhat, S
dc.contributor.authorByanju, R
dc.contributor.authorKhadka, S
dc.date.accessioned2025-12-21T07:05:11Z
dc.date.available2025-12-21T07:05:11Z
dc.date.issued2021
dc.descriptionRanabhat S,1 Byanju R,1 Khadka S2 1Department of Vitreo-retina Bharatpur Eye Hospital Bharatpur, Chitwan, Nepal 2Department of Vitreo-retina Nepal Eye Hospital Kathmandu, Nepal
dc.description.abstractABSTRACT Behcet’s disease is a multisystemic vasculitis of unknown etiopathogenesis characterized by recurrent acute inflammation. A 30-year male presented with progressive blurred vision in both eye for one month associated with photophobia, redness and ocular pain. On presentation best corrected visual acuity was 6/9 both eyes. Bilateral ocular examination of anterior segment demonstrated occasional cells. Treatment history of multiple joint pain along with oral aphthous ulcers. Erythematous papulopustular lesion over face, neck, trunk and genital ulcers were being treated. Irrespective of negative human leucocyte antigen B51 and pathergy, patient was diagnosed as Behcet’s disease on the basis of clinical criteria and started with topical steroid and cycloplegic. At one-month, ocular symptoms were relieved. Behcet’s disease is a rare, autoimmune disease, which lacks universal pathognomonic test and investigations, therefore diagnosis is primarily done with international criteria for Behcet’s disease. Multidisciplinary approach certainly helps in early diagnosis and eliminating morbidity. KEY WORDS Behcet’s disease, HLAB51, Pathergy test, Silk road, Uveitis
dc.identifier.urihttps://hdl.handle.net/20.500.14572/3738
dc.language.isoen_US
dc.publisherKathmandu University
dc.subjectBehcet’s disease
dc.subjectHLAB51
dc.subjectPathergy test
dc.subjectSilk road
dc.subjectUveitis
dc.titleBehcet’s Disease with Absent HLA Serotyping and Pathergy Test
dc.typeArticle
dspace.entity.typePublication
local.article.typeCase Report
oaire.citation.endPage521
oaire.citation.startPage519
relation.isJournalIssueOfPublication15eeb083-e217-49bb-bea1-16142e5271e1
relation.isJournalIssueOfPublication.latestForDiscovery15eeb083-e217-49bb-bea1-16142e5271e1
relation.isJournalOfPublicationa782b7ff-cf89-4178-ad1c-11ed89cfe1bd

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