Isolated conjunctival amyloidosis--a case report.
dc.contributor.author | Jaswal, T S | en_US |
dc.contributor.author | Singh, Sunita | en_US |
dc.contributor.author | Gupta, Veena | en_US |
dc.contributor.author | Kalra, Rajneesh | en_US |
dc.contributor.author | Srivastava, Monika | en_US |
dc.contributor.author | Arora, B | en_US |
dc.date.accessioned | 2003-04-17 | en_US |
dc.date.accessioned | 2009-05-29T11:25:27Z | |
dc.date.available | 2003-04-17 | en_US |
dc.date.available | 2009-05-29T11:25:27Z | |
dc.date.issued | 2003-04-17 | en_US |
dc.description.abstract | Isolated conjunctival amyloidosis is extremely rare and usually diagnosed histologically instead of clinically. This has been variously reported as an unusual cause of ptosis, complication of trachoma, painless nodular aggregates and recurrent subconjunctival hemorrhages. Once diagnosed, evaluation for systemic disease is advised though results of examination are almost always negative and frustrating. | en_US |
dc.description.affiliation | Department of Pathology, Pt. B.D. Sharma PGIMS, Rohtak. | en_US |
dc.identifier.citation | Jaswal TS, Singh S, Gupta V, Kalra R, Srivastava M, Arora B. Isolated conjunctival amyloidosis--a case report. Indian Journal of Pathology & Microbiology. 2003 Apr; 46(2): 235-6 | en_US |
dc.identifier.uri | https://imsear.searo.who.int/handle/123456789/73499 | |
dc.language.iso | eng | en_US |
dc.source.uri | https://www.ijpmonline.org | en_US |
dc.subject.mesh | Amyloidosis --diagnosis | en_US |
dc.subject.mesh | Conjunctival Diseases --diagnosis | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Male | en_US |
dc.subject.mesh | Middle Aged | en_US |
dc.title | Isolated conjunctival amyloidosis--a case report. | en_US |
dc.type | Case Reports | en_US |
dc.type | Journal Article | en_US |
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