scholarly journals A Rare Case of Pulmonary Hypertension

2005 ◽  
Vol 46 (3) ◽  
pp. 551-556 ◽  
Author(s):  
Gülsah Tayyareci ◽  
Sennur Ünal Dayi ◽  
Haldun Akgöz ◽  
Sait Terzi ◽  
Tamer Akbulut ◽  
...  
CHEST Journal ◽  
2014 ◽  
Vol 145 (3) ◽  
pp. 64A
Author(s):  
Ram K. Chopra ◽  
Sanesh Garde ◽  
Chintan Patel ◽  
Dhiraj Jain ◽  
Omkar Kajale ◽  
...  

2018 ◽  
Vol 71 (11) ◽  
pp. A2445
Author(s):  
Tieci Yi ◽  
Wenhui Ding ◽  
Wei Ma

2021 ◽  
pp. 1-5
Author(s):  
Mohammad Mahdavi ◽  
Sanaz Asadian ◽  
Nahid Rezaeian ◽  
Sahar Asl Fallah ◽  
Hossein Shahzadi ◽  
...  

Abstract Chronic thromboembolic pulmonary hypertension is an uncommon condition in the children. It almost always accompanies a hypercoagulable state. We described a rare case of Behçet’s disease presenting with chronic thromboembolic pulmonary hypertension and initially misdiagnosed as coronavirus disease 2019 pneumonia.


2020 ◽  
Vol 25 (2) ◽  
pp. 23-27
Author(s):  
Fahisham Taib ◽  
Nur Atiqah Abdul Rahman ◽  
Mohd Rizal Mohd Zain

Cor-triatriatum is a rare cardiac anomaly. In literature, majority case reports on the condition focused on its late presentation in adulthood. It can be easily corrected by surgical intervention to avoid pulmonary congestion and subsequent pulmonary hypertension. We report a rare case of cor-triatriatum with severe pulmonary hypertension in a 7-week-old baby who presented with persistent tachypnoea.


2019 ◽  
Vol 09 (08) ◽  
pp. 1151-1160
Author(s):  
Wiryawan Permadi ◽  
Dani Setiawan ◽  
Muhammad Alamsyah Aziz ◽  
Yanuarman   ◽  
Anita D. Anwar ◽  
...  

Author(s):  
Filippo Ghidini ◽  
Biagio Castaldi ◽  
Massimo Padalino ◽  
Patrizia Dall'Igna

A rare case of mixed total anomalous pulmonary venous connection (TAPVC) associated to right extra-lobar bronchopulmonary sequestration (BPS) was diagnosed at birth in a full-term newborn. At one month of age, the patient underwent embolization of the BPS, complicated by coil entrapment in the right common iliac artery requiring urgent laparotomy. Few days later, the congenital cardiac repair was accomplished uneventfully. At 12-months follow-up, the patient did not have pulmonary hypertension, but presented a moderate stenosis of the right femoral artery, which was effectively treated with anticoagulation therapy.


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