Familial Sarcoidosis: An Analysis of Twenty-Eight Cases
Objective: 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 c...
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Wolters Kluwer Medknow Publications
2016-12-01
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doaj-4d57fb4251d14e4e8dcc306eefe4dabd2020-11-24T23:55:38ZengWolters Kluwer Medknow PublicationsEurasian Journal of Pulmonology 2148-36202148-54022016-12-0118314314710.5152/ejp.2016.28863Familial Sarcoidosis: An Analysis of Twenty-Eight CasesDildar Duman0Tülin Sevim1Lale Sertçelik2Olga Akkan3Sinem Güngör4Murat Yalçınsoy5İpek Erdem6Reyhan Yıldız7Sümeyye Bekir8Murat Kavas9Armağan Hazar10Esen Akkaya11Department of Pulmonology, Süreyyapaşa Chest Diseases and Thoracic Surgery Trainig and Research Hospital, İstanbul, TurkeyDepartment of Pulmonology, Süreyyapaşa Chest Diseases and Thoracic Surgery Trainig and Research Hospital, İstanbul, TurkeyDepartment of Pulmonology, Süreyyapaşa Chest Diseases and Thoracic Surgery Trainig and Research Hospital, İstanbul, TurkeyDepartment of Pulmonology, Süreyyapaşa Chest Diseases and Thoracic Surgery Trainig and Research Hospital, İstanbul, TurkeyDepartment of Pulmonology, Süreyyapaşa Chest Diseases and Thoracic Surgery Trainig and Research Hospital, İstanbul, TurkeyDepartment of Pulmonology, İnönü University School of Medicine, Malatya, TurkeyDepartment of Pulmonology, Süreyyapaşa Chest Diseases and Thoracic Surgery Trainig and Research Hospital, İstanbul, TurkeyDepartment of Pulmonology, Süreyyapaşa Chest Diseases and Thoracic Surgery Trainig and Research Hospital, İstanbul, TurkeyDepartment of Pulmonology, Süreyyapaşa Chest Diseases and Thoracic Surgery Trainig and Research Hospital, İstanbul, TurkeyDepartment of Pulmonology, Süreyyapaşa Chest Diseases and Thoracic Surgery Trainig and Research Hospital, İstanbul, TurkeyDepartment of Pulmonology, Süreyyapaşa Chest Diseases and Thoracic Surgery Trainig and Research Hospital, İstanbul, TurkeyDepartment of Pulmonology, Süreyyapaşa Chest Diseases and Thoracic Surgery Trainig and Research Hospital, İstanbul, TurkeyObjective: 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.http://www.eurasianjpulmonol.com/jvi.aspx?pdir=eurasianjpulmonol&plng=eng&un=EJP-28863Familialmediastinoscopy |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Dildar Duman Tülin Sevim Lale Sertçelik Olga Akkan Sinem Güngör Murat Yalçınsoy İpek Erdem Reyhan Yıldız Sümeyye Bekir Murat Kavas Armağan Hazar Esen Akkaya |
spellingShingle |
Dildar Duman Tülin Sevim Lale Sertçelik Olga Akkan Sinem Güngör Murat Yalçınsoy İpek Erdem Reyhan Yıldız Sümeyye Bekir Murat Kavas Armağan Hazar Esen Akkaya Familial Sarcoidosis: An Analysis of Twenty-Eight Cases Eurasian Journal of Pulmonology Familial mediastinoscopy |
author_facet |
Dildar Duman Tülin Sevim Lale Sertçelik Olga Akkan Sinem Güngör Murat Yalçınsoy İpek Erdem Reyhan Yıldız Sümeyye Bekir Murat Kavas Armağan Hazar Esen Akkaya |
author_sort |
Dildar Duman |
title |
Familial Sarcoidosis: An Analysis of Twenty-Eight Cases |
title_short |
Familial Sarcoidosis: An Analysis of Twenty-Eight Cases |
title_full |
Familial Sarcoidosis: An Analysis of Twenty-Eight Cases |
title_fullStr |
Familial Sarcoidosis: An Analysis of Twenty-Eight Cases |
title_full_unstemmed |
Familial Sarcoidosis: An Analysis of Twenty-Eight Cases |
title_sort |
familial sarcoidosis: an analysis of twenty-eight cases |
publisher |
Wolters Kluwer Medknow Publications |
series |
Eurasian Journal of Pulmonology |
issn |
2148-3620 2148-5402 |
publishDate |
2016-12-01 |
description |
Objective: 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. |
topic |
Familial mediastinoscopy |
url |
http://www.eurasianjpulmonol.com/jvi.aspx?pdir=eurasianjpulmonol&plng=eng&un=EJP-28863 |
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