scholarly journals MANAGING A RARE CASE OF CONGENTIAL ATRESIA OF THE LEFT SUPERIOR PULMONARY VEIN WITH ASSOCIATED ATYPICAL CORONARY ANATOMY IN AN ADULT PATIENT WITH NEW ONSET SELF LIMITED CHEST PAIN

CHEST Journal ◽  
2021 ◽  
Vol 160 (4) ◽  
pp. A1648
Author(s):  
Ralph Maroun ◽  
Samuel Treat ◽  
Taylor Oakley ◽  
Jared Kravitz
2018 ◽  
Vol 28 (4) ◽  
pp. 595-597
Author(s):  
Kamran Ahmadov ◽  
Catherine A. Beigelman ◽  
Matthias Kirsch

AbstractA rare case of Scimitar Syndrome with an abnormal drainage of the right lower pulmonary vein into the right superior pulmonary vein associated with aortic root aneurism and bicuspid aortic valve is reported.


2020 ◽  
Vol 6 (1) ◽  
Author(s):  
Go Kamimura ◽  
Kazuhiro Ueda ◽  
Koki Maeda ◽  
Masaya Aoki ◽  
Toshiyuki Nagata ◽  
...  

2011 ◽  
Vol 31 (9) ◽  
pp. 969-973
Author(s):  
Zhi-jian YANG ◽  
Yang XIA ◽  
Liang ZHAO ◽  
Jia-you ZHANG ◽  
Shu-jun JIANG ◽  
...  

2008 ◽  
Vol 63 (2) ◽  
pp. 265-269
Author(s):  
C. Scavée ◽  
A. Brasseur ◽  
R. Weerasooriya

2018 ◽  
Vol 4 (11) ◽  
pp. 553-555
Author(s):  
Marina Arai ◽  
Seiji Fukamizu ◽  
Rintaro Hojo ◽  
Masayasu Hiraoka

2011 ◽  
Vol 22 (8) ◽  
pp. 943-944 ◽  
Author(s):  
XINGPENG LIU ◽  
SHINSUKE MIYAZAKI ◽  
ASHOK SHAH ◽  
MICHEL HAÏSSAGUERRE ◽  
MELEZE HOCINI

Cancer ◽  
1990 ◽  
Vol 66 (4) ◽  
pp. 789-795 ◽  
Author(s):  
Larry R. Kaiser ◽  
Carlos Urmacher

2021 ◽  
Vol 14 (4) ◽  
pp. e242412
Author(s):  
Suthaphong Tripoppoom ◽  
Nophol Leelayuwatanakul

Haemorrhage in patients with haemophilia is common after minor trauma but may occur spontaneously. Despite the diversity of bleeding sites, spontaneous haemothorax, on a non-traumatic basis, is an exceedingly rare event and only a few cases had been reported. We present a case of a 43-year-old man with a history of haemophilia A who had pleuritic chest pain for 1 day without significant history of trauma. Diagnostic thoracentesis showed bloody pleural fluid in which neither abnormal cell nor organism was found. He was treated by cryoprecipitate replacement and therapeutic thoracentesis for releasing haemothorax. After discharge, the patient returned for follow-up with complete radiological resolution. Regarding the consequences of retained haemothorax from conservative approach and the procedure-related bleeding of given therapeutic intervention in haemothorax making its management in patients with haemophilia to be more challenging. Our case illustrates a conservative treatment of spontaneous haemothorax in patient with haemophilia resulting in a good clinical outcome.


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