Familial Sarcoidosis: An Analysis of Twenty-Eight Cases

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dc.authoridDuman, Dildar/0000-0001-8680-8550
dc.authoridYalçınsoy, Murat/0000-0003-3407-7359
dc.authoridGungor, Sinem/0000-0002-1163-125X
dc.authoridduman, dildar/0000-0001-8680-8550
dc.authorwosidDuman, Dildar/GQH-4100-2022
dc.authorwosidYalçınsoy, Murat/ABI-1421-2020
dc.authorwosidGungor, Sinem/AAZ-7783-2021
dc.authorwosidGungor, Sinem/GPX-1807-2022
dc.authorwosidKavas, Murat/HNT-0352-2023
dc.authorwosidduman, dildar/JCO-7473-2023
dc.contributor.authorDuman, Dildar
dc.contributor.authorSevim, Tulin
dc.contributor.authorSertcelik, Lale
dc.contributor.authorAkkan, Olga
dc.contributor.authorGungor, Sinem
dc.contributor.authorYalcinsoy, Murat
dc.contributor.authorErdem, Ipek
dc.date.accessioned2024-08-04T20:10:27Z
dc.date.available2024-08-04T20:10:27Z
dc.date.issued2016
dc.departmentİnönü Üniversitesien_US
dc.description.abstractObjective: Sarcoidosis is a multisystemic disease, exact cause of disease is unknown but it is assumed that genetic predisposition and ethnic factors play a role in etiology. Studies related with familial sarcoidosis is limited and only case reports about familial sarcoidosis is available from our country. We aimed to evaluate the prevelance of familial sarcoidosis and clinical findings of cases with familial sarcoidosis. Methods: We retrospectively documented file records of 678 patients diagnosed with sarcoidosis and followed up in outpatient clinic of sarcoidosis from January 1996 to February 2016. 28 familial sarcoidosis cases in 14 families were enrolled into the study. Their demographic findings, family relationship, symptoms, laboratory and pulmonary function test results, radiological apperances, diagnostic methods, treatments were recorded. Results: Twenty-eight sarcoidosis patients out of 678 reported as familial cases, giving a prevelance of familial sarcoidosis as 4%. There were 8 sarcoidosis sib, 4 sarcoidosis mother-child, 1 sarcoidosis father-child and 1 sarcoidosis cousin relationship. Female/male ratio was 1.8, mean age of the study population was 43, most freguent symptoms were cough and dyspnea, stage 2 was mostly seen according to chest X-ray, most common CT appearance was mediastinal lymphadenopathy and mediastinoscopy was the most freguent diagnostic method. Conclusion: This study is important to lead interrogation of family in patients with suspected sarcoidosis and future studies investigating familial aggregation in sarcoidosis.en_US
dc.identifier.doi10.5152/ejp.2016.28863
dc.identifier.endpage147en_US
dc.identifier.issn2148-3620
dc.identifier.issn2148-5402
dc.identifier.issue3en_US
dc.identifier.startpage143en_US
dc.identifier.trdizinid217007en_US
dc.identifier.urihttps://doi.org/10.5152/ejp.2016.28863
dc.identifier.urihttps://search.trdizin.gov.tr/yayin/detay/217007
dc.identifier.urihttps://hdl.handle.net/11616/92790
dc.identifier.volume18en_US
dc.identifier.wosWOS:000391006500007en_US
dc.identifier.wosqualityN/Aen_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakTR-Dizinen_US
dc.language.isoenen_US
dc.publisherAvesen_US
dc.relation.ispartofEurasian Journal of Pulmonologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectFamilialen_US
dc.subjectmediastinoscopyen_US
dc.subjectsarcoidosisen_US
dc.titleFamilial Sarcoidosis: An Analysis of Twenty-Eight Casesen_US
dc.typeArticleen_US

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