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dc.contributor.authorYazici, Y
dc.contributor.authorYazici, H
dc.contributor.authorSanders, A
dc.contributor.authorTrost, D
dc.contributor.authorErkan, D
dc.date.accessioned2021-03-03T11:37:46Z
dc.date.available2021-03-03T11:37:46Z
dc.date.issued2004
dc.identifier.citationErkan D., Yazici Y., Sanders A., Trost D., Yazici H., "Is Hughes-Stovin syndrome Behcet's disease?", CLINICAL AND EXPERIMENTAL RHEUMATOLOGY, cilt.22, sa.4, 2004
dc.identifier.issn0392-856X
dc.identifier.othervv_1032021
dc.identifier.otherav_2902ef27-8721-4595-b334-42216a5c44cf
dc.identifier.urihttp://hdl.handle.net/20.500.12627/32407
dc.description.abstractHughes-Stovin syndrome (HSS) is a rare clinical disorder, which has been described as the presence of pulmonary artery aneurysm in the setting of systemic thrombosis. The term "Incomplete Behcet's Disease" has also been used to describe this syndrome due to the clinical and histopathological similarities between Behcets disease and HSS. Indeed, pulmonary involvement can be indistinguishable between these two conditions of unknown pathophysiology. We describe an HSS patient who presented with a recurrent pulmonary artery aneurysm, review the clinical and pathological manifestations of HSS, discuss its similarities to Behcet's disease, and finally make the argument that HSS is in fact Behcet's disease.
dc.language.isoeng
dc.subjectİmmünoloji ve Romatoloji
dc.subjectDahili Tıp Bilimleri
dc.subjectİç Hastalıkları
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectROMATOLOJİ
dc.titleIs Hughes-Stovin syndrome Behcet's disease?
dc.typeMakale
dc.relation.journalCLINICAL AND EXPERIMENTAL RHEUMATOLOGY
dc.contributor.department, ,
dc.identifier.volume22
dc.identifier.issue4
dc.contributor.firstauthorID172092


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