scholarly journals Effects of corticosteroid and chlorambucil on multiple pulmonary artery aneurysms in Behcet's syndrome: A case repor

1995 ◽  
Vol 10 (6) ◽  
pp. 470 ◽  
Author(s):  
Jae Yong Park ◽  
Jun Goo Park ◽  
Jun Hee Won ◽  
Jong Myung Lee ◽  
Nung Soo Kim ◽  
...  
2016 ◽  
Vol 102 (4) ◽  
pp. e363 ◽  
Author(s):  
Sedat Giray Kandemirli ◽  
Mehmet Cingoz ◽  
Emel Ure ◽  
Selim Bakan ◽  
Canan Akman

2021 ◽  
Vol 15 (1) ◽  
Author(s):  
Ziyad Alakkas ◽  
Waad Kazi ◽  
Mohamed Mattar ◽  
Eman Abdul Wahhab Salem ◽  
Naglaa Fawzy Seleem

Abstract Background Behçet’s syndrome is a type of systemic chronic vasculitis of unknown etiology, frequently characterized by recurrent oral and genital ulcers and uveitis. It is less commonly characterized by arthritis and skin, vascular, and gastrointestinal involvements. Behçet’s syndrome affects various sizes of vessels by perivascular infiltration and vasculitis. Unlike other classic types of vasculitis, Behçet’s syndrome patients can present with both arterial and venous involvement. Although vascular Behçet’s syndrome is found in only around 15% of Behçet’s syndrome patients, it is the major cause of morbidity and mortality among them. Furthermore, although deep venous thrombosis has high incidence in Behçet’s syndrome patients, pulmonary artery thrombosis is an uncommon complication. Combining the findings of this and previous case reports of pulmonary artery thrombosis in Behçet’s syndrome patients, we sought to determine the best treatment options for pulmonary artery thrombosis in Behçet’s syndrome patients. Case presentation We present the case of a 22-year-old Arabian male who was admitted to an emergency department with acute chest pain, dyspnea, and hemoptysis for 2 weeks. He gave a long history of recurrent oral and genital ulcers for the last 4 months but without seeking medical advice. Spiral computed tomography showed arterial filling defects with a pulmonary nodule for which the presence of a pulmonary artery aneurysm ruled out. The lung perfusion scan showed multiple pulmonary perfusion defects. After excluding common infectious diseases such as tuberculosis and brucellosis, a diagnosis of Behçet’s syndrome with pulmonary artery thrombosis was made. Steroids with enoxaparin were initiated. The patient was discharged later on prednisolone (tapering dose) with adalimumab and apixaban. He was on regular follow-up for the next 9 months. Conclusions Vascular involvement in Behçet’s syndrome is a major contributor to morbidity and mortality of Behçet’s syndrome patients. Consequently, early detection of vascular involvement has a major impact on the prognosis of patients with Behçet’s syndrome.


2011 ◽  
Vol 105 (11) ◽  
pp. 1739-1747 ◽  
Author(s):  
Emire Seyahi ◽  
Murat Baskurt ◽  
Melike Melikoglu ◽  
Canan Akman ◽  
Deniz Cebi Olgun ◽  
...  

2021 ◽  
Author(s):  
Didem Sahin Eroglu ◽  
Anil Colaklar ◽  
Alparslan Ceran ◽  
Serdar Sezer ◽  
Murat Torgutalp ◽  
...  

ZusammenfassungDie Beteiligung der Lungenarterie ist eine seltene, aber tödliche Komplikation des Morbus Behçets (MB). Hier berichten wir über einen männlichen MB-Patienten mit zwei vaskulären Komplikationen, nämlich dem Budd-Chiari-Syndrom und der Pulmonalarterienthrombose. Der Patient litt unter einer rezidivierenden Lungenarterienthrombose, die gegen mehrere immunsuppressive Medikamente, einschließlich hochdosierter Glukokortikoide und dem Anti-TNF-Mittel Infliximab, refraktär war. Infolge mehrerer Rezidive wurde er effektiv mit Tocilizumab behandelt, wodurch auch eine vollständige Rekanalisation der thrombosierten Arterien erreicht wurde.


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