Unusual radiological manifestations of rare complications of cardiovascular Behcet disease (BD) are the following: (a) aneurysm and (b) occlusion in the aorta and its major branches, (c) pseudoaneurysms on the aortic root and coronary artery, and recurrent valvular dehiscence in the heart, (d) venous thrombosis in the deep and superficial venous system and vena cava. The initial exact diagnosis of cardiovascular BD has been extremely difficult for these rare complicated findings, especially in the absence of the florid clinical manifestations of BD. Radiologist should be aware of possibility of cardiovascular BD via familiarity with its rare imaging features, including computed tomographic angiography (and its 3-dimensional reconstructed images), conventional angiography, and with the clinical characteristics of BD because of high mortality of cardiovascular BD.
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http://dx.doi.org/10.1097/RCT.0b013e3181573282 | DOI Listing |
Eur J Heart Fail
December 2024
Department of Cardiology, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.
Aims: Although certain autoimmune diseases (AIDs) have been associated with an increased rate of heart failure (HF), data on the long-term rate of HF across the spectrum of AIDs are lacking. We investigated the long-term rate of HF in individuals with a history of 28 different AIDs.
Methods And Results: Individuals diagnosed with an AID (2000-2021) were identified through Danish nationwide registries.
Int J Rheum Dis
December 2024
Department of Rheumatology and Immunology, Peking University International Hospital, Beijing, China.
Behcet's disease is a rare, chronic inflammatory disorder that can affect various organs, with large vessel involvement being particularly uncommon. This case report discusses a 17-year-old male with Behcet's disease who presented with a rapidly enlarging, painful mass in the right groin region, later diagnosed as a femoral artery aneurysm. The patient underwent successful surgical intervention and was subsequently managed with immunosuppressive therapy to prevent relapse.
View Article and Find Full Text PDFCurr Opin Rheumatol
December 2024
Division of Rheumatology and Clinical Immunology, Department of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.
Purpose Of Review: Ongoing research contributes to our understanding of the epidemiology of vasculitis and its outcomes across the globe. This review aims to summarize important research studies published on this topic in the last 18 months.
Recent Findings: The implementation of rapid referral systems and use of large vessel imaging have improved the diagnosis of giant cell arteritis.
Cureus
November 2024
Gynecology, CosmeSurge Group, Dubai, ARE.
Behçet's disease (BD) is a systemic auto-inflammatory vasculitis. The clinical pictures of BD involve the skin and mucosal membranes such as oral and genital ulcers, ocular lesions, cardiovascular, gastrointestinal, muscular, nervous systems, and joints. A 38-year-old woman was repeatedly suffering from oral, genital, and ocular lesions, wound dehiscence after any surgical procedure, and joint pain.
View Article and Find Full Text PDFClin Rheumatol
November 2024
Department of Rheumatology and Immunology, Capital Institute of Pediatrics, Beijing, China.
Objectives: To review the clinical features, treatment, and prognosis of coronary involvement in Behcet's syndrome in children.
Methods: Retrospectively analyzed medical records of BS patients admitted to our institution from 2012 to 2024.
Results: Six children with BS with coronary involvement were admitted, including 2 males and 4 females.
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