scholarly journals Gastric Mass: Intramural Hematoma

Cureus ◽  
2021 ◽  
Author(s):  
Kathryn Schwalbe ◽  
Abhiram Kondajji ◽  
Matthew T Allemang
2019 ◽  
Vol 114 (1) ◽  
pp. S1119-S1119
Author(s):  
Edwin J. Lee ◽  
Shivangi Kothari ◽  
Truptesh Kothari ◽  
Vivek Kaul

1973 ◽  
Vol 108 (6) ◽  
pp. 839-841
Author(s):  
M. J. Tye
Keyword(s):  

2012 ◽  
Vol 4 (3) ◽  
pp. 200-207
Author(s):  
Toshimitsu Takagi ◽  
Yuki Horita ◽  
Naoto Tama ◽  
Hidenobu Terai ◽  
Isao Inoki ◽  
...  

2012 ◽  
Vol 15 (5) ◽  
pp. 286
Author(s):  
Jan Droste ◽  
Heidar Zafarani Zadeh ◽  
Mohammed Arif ◽  
Ian Craig ◽  
A K Thakur

<p>A patient presented with recurrent syncope due to transient severe hypotension. The patient's history, physical examination, and initial baseline investigation did not suggest a cardiovascular cause. After fluid resuscitation, a raised jugular venous pulse was noted. Bedside transthoracic echocardiogram showed a pericardial effusion and a proximally dilated aorta. Computed tomography of the thorax confirmed these findings and also demonstrated an intramural hematoma of the proximal aortic wall.</p><p>The patient was transferred to a cardiothoracic center, where he was at first treated medically. He then developed sudden cardiogenic shock due to pericardial tamponade and was successfully operated on.</p><p>It is important to recognize an acute intramural hematoma of the proximal aortic wall as a cardiothoracic emergency. This condition can present atypically, but nevertheless warrants urgent surgical intervention, equal to type A aortic dissection. Echocardiography can help in making the diagnosis.</p>


Author(s):  
Tolga Canbak ◽  
Aylin Acar ◽  
Fatih Basak ◽  
Ali Kilic ◽  
Metin Yucel ◽  
...  

2003 ◽  
Vol 10 (2) ◽  
pp. 392-396 ◽  
Author(s):  
Marco Ventura ◽  
Alessandro Mastromarino ◽  
Lucia Cucciolillo ◽  
Giuseppe Calvisi ◽  
Carlo Spartera

2020 ◽  
Vol 13 (12) ◽  
pp. e236855
Author(s):  
Wendy Chang ◽  
Patricia Renaut ◽  
Casper Pretorius

Juvenile polyposis syndrome (JPS) and hereditary haemorrhagic telangiectasia (HHT) are rare autosomal dominant diseases, where symptoms manifest at childhood. A 32-year-old man with no family history of JPS or HHT with SMAD4 gene mutation who developed signs and symptoms only at the age of 32, when he was an adult. In this article, we highlight the steps taken to diagnose this rare pathology, explain its pathophysiology and management.


2002 ◽  
Vol 56 (5) ◽  
pp. 767-770 ◽  
Author(s):  
Michael Meininger ◽  
Manjit Bains ◽  
Siaka Yusuf ◽  
Hans Gerdes

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