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Swyer-James-Macleod Sendromu ve Antifosfolipid Antikor Sendromu: Nadir Bir Olgu Sunumu
2021
Journal:  
Respiratory Case Reports
Author:  
Abstract:

Swyer-James-Macleod sendromu (SJMS), etiyolojisinde çocukluk çağı alt solunum yolu enfeskiyonlarının yer aldığı düşünülen obliteratif bronşiolitis durumudur. Hastalar ileri yaşlara kadar tanı alamayabilir. Noninvaziv toraks görüntüleme yöntemleri ve öykü ile tanısı konulmaktadır. Antifosfolipid antikor sendromu (AFAS) tekrarlayan vasküler tromboz, nedeni açıklanamayan fetal kayıplar ve trombositopeni ile seyreden multisistemik otoimmün bir hastalıktır. Hastaların yüzde 70’i kadındır. Erkek hastalar için de tekrarlayan veya olağan dışı trombozlarda ve genç yaştaki unprovake trombozu olan olgularda ayırıcı tanıda akılda tutulmalıdır. Akut periferik trombüs klinik tablosunda başvuran 33 yaşındaki erkek olgu dispne nedeniyle göğüs hastalıklarına konsülte edildi ve SJMS tanısı aldı. Takiplerde, yapılan ileri tetkikler sonrasında, hastaya AFAS tanısı konuldu. Olgumuz, nadir görülen bu iki sendromun eş zamanlı birlikteliği nedeniyle bildirilmiştir.

Keywords:

Swyer-James-Macleod Syndrome and Antiphospholipid Syndrome: A Rare Fact Presentation
2021
Author:  
Abstract:

Swyer-James-Macleod syndrome (SJMS) is a condition of obliterative bronchiolitis, which is believed to include infection in childhood in its etiology. Patients may not be diagnosed up to age. Non-invasive thorax is diagnosed with the methods of imaging and history. Antifospholipid antibodies syndrome (AFAS) is a repeated vascular thrombosis, a multisystemic autoimmune disease that is associated with unexplicable cause of fetal losses and trombocytopenia. 70 percent of patients are women. The distinctive diagnosis should also be taken into account for male patients with repeated or unusual thrombosis and unprovake thrombosis in young age. A 33-year-old man who applied to the clinical table of acute peripheral thrombus was consulted for breast diseases due to the occurrence of dyspnoe and was diagnosed with SJMS. In the follow-up, after advanced examinations, the patient was diagnosed with AFAS. Our case is due to the simultaneous association of these two rare syndrome.

Keywords:

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2021
Author:  
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Respiratory Case Reports

Field :   Sağlık Bilimleri

Journal Type :   Uluslararası

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Article : 120
Respiratory Case Reports