scholarly journals Type A aortic dissection presenting as superior vena cava syndrome

CJEM ◽  
2013 ◽  
Vol 15 (01) ◽  
pp. 59-62 ◽  
Author(s):  
Faisal S. Raja ◽  
Ali Islam ◽  
Mustafa Khan ◽  
Iram Abbasi

ABSTRACT A 51-year-old man presented with a 5-day history of progressive facial swelling, sensation of head fullness, increasing shortness of breath and paroxysmal nocturnal dyspnea. He denied chest pain, syncope or presyncope. Pastmedical history included mechanical aortic valve replacement 7 years prior and atrial fibrillation treated with warfarin. A clinical diagnosis of acute superior vena cava (SVC) syndrome was made. Portable chest radiograph showed a widened superior mediastinum. Computed tomography scan of the thorax demonstrated a large type A aortic dissection almost completely effacing the SVC. Acute type A aortic dissection (AD) is an emergency requiring prompt diagnosis and treatment. Patients typically present with acute onset of chest and/or back pain, classically described as “ripping” or “tearing.” SVC syndrome is rarely, if ever, mentioned as a presentation, as it is usually due to more chronic conditions. This case illustrates a rare incidence of type A AD actually presenting as SVC syndrome.

2000 ◽  
Vol 69 (6) ◽  
pp. 1940-1941 ◽  
Author(s):  
Charles R. Bridges ◽  
Robert C. Gorman ◽  
Mark M. Stecker ◽  
Joseph E. Bavaria

2012 ◽  
Vol 20 (4) ◽  
pp. 466-468
Author(s):  
Yukihiro Matsuno ◽  
Narihiro Ishida ◽  
Yukiomi Fukumoto ◽  
Katsuya Shimabukuro ◽  
Hirofumi Takemura

2015 ◽  
Vol 4 (3) ◽  
pp. 2 ◽  
Author(s):  
Mitra Chitsazan ◽  
Ziae Totonchi ◽  
Nader Givtaj ◽  
Mozhgan Sakhaei ◽  
Afshin Foroutan ◽  
...  

CJEM ◽  
1999 ◽  
Vol 1 (02) ◽  
pp. 112-114
Author(s):  
Laura A. Price ◽  
Trevor L. Gilkinson

SUMMARY: A 41-year-old man was brought to the ED after a motor vehicle crash. On presentation, he demonstrated symptoms compatible with superior vena cava (SVC) syndrome, including extreme dyspnea, face and neck cyanosis and facial swelling. A chest tube was inserted and drained large amounts of sanguineous fluid. An exploratory thoracotomy revealed an extensive tumour encasing the SVC and the hilum. Biopsy confirmed the diagnosis of T-cell lymphoma. The most common cause of SVC syndrome is malignant disease, with bronchogenic carcinoma and lymphoma being most frequent. Review of the literature uncovered only a few anecdotal reports of traumatic SVC syndrome. There are no previous reported cases of malignant SVC syndrome presenting in association with trauma.


2020 ◽  
Vol 13 (6) ◽  
pp. e234345
Author(s):  
Kale S Bongers ◽  
Vaiibhav Patel ◽  
Sarah K Gualano ◽  
Richard J Schildhouse

Superior vena cava (SVC) syndrome results from the blockage of venous blood flow through the SVC, which is caused by either internal obstruction (eg, thrombus) or external compression (eg, thoracic malignancy and infection).1 While thrombus-related SVC syndrome is rising in prevalence, malignancy still accounts for the majority of cases.1 Regardless of cause, SVC syndrome is characterised by facial swelling and plethora, headache and dyspnoea.2 Although venous stenting has become standard of care for treatment of acute SVC syndrome, stent placement presents multiple risks including SVC rupture and cardiac tamponade. In these cases, a high index of suspicion and prompt action are required to avoid an often fatal outcome. Here, we present the case of a patient with cardiac tamponade and subsequent cardiac arrest after SVC stent placement.


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