scholarly journals Rare Presentation of Pulmonary Hypertension in a Young Patient

2020 ◽  
Vol 4 (1) ◽  
Author(s):  
Shailee Jain ◽  
Prasanna Sengodan ◽  
Deepak Donthi ◽  
Marwan Majeed ◽  
Mark Williams ◽  
...  
2021 ◽  
Vol 22 ◽  
pp. 101064
Author(s):  
Hana Mahallati ◽  
James Kirkland Roberts ◽  
Amer Assal ◽  
Divaya Bhutani ◽  
David C. Park ◽  
...  

2020 ◽  
Vol 8 ◽  
pp. 2050313X2096904
Author(s):  
Constanza Burciaga Calderoni ◽  
Dafne T Moretta ◽  
Jeanette Merrill-Henry ◽  
Paresh C Giri

Pulmonary tumor thrombotic microangiopathy is a rare condition in which embolization of tumor cells to the pulmonary arterioles causes fibrocellular intimal thickening and activation of the coagulation cascade resulting in pulmonary hypertension and right heart failure. Herein, we highlight a young 35-year-old male with no known past medical history who presented with recurrent syncope and dyspnea, and was found to have severe right heart failure and pulmonary hypertension. He developed sudden clinical deterioration and died after a cardiac arrest. Autopsy revealed poorly differentiated gastric adenocarcinoma and pulmonary tumor thrombotic microangiopathy. New onset severe pulmonary hypertension and right heart failure without any other obvious etiology should encourage the reader to evaluate for pulmonary tumor thrombotic microangiopathy and undergo a diligent search for underlying malignancy. This case highlights recurrent syncope as a rare presentation of this rapidly fatal disease.


1993 ◽  
Vol 32 (4) ◽  
pp. 461-462 ◽  
Author(s):  
Vadavattath Padmanabhan Gangadharan ◽  
Kesavan Chitrathara ◽  
Ramachandran Sivaramakrishnan ◽  
Kochunarayanan Satishkumar ◽  
Madhavan Krishnan Nair

2011 ◽  
Vol 10 (2) ◽  
pp. 128-128
Author(s):  
Jessa Scott

In this issue of Advances in Pulmonary Hypertension, Editor-in-Chief Erika Rosenzweig, MD, asked a former patient: Can you give us your first-hand perspective, the good and the bad, as a young patient dealing with pulmonary hypertension?


2015 ◽  
Vol 2015 ◽  
pp. 1-2 ◽  
Author(s):  
Francesco Raimondi ◽  
Fiorella Migliaro ◽  
Elisa Di Pietro ◽  
Francesco Borgia ◽  
Antonio Rapacciuolo ◽  
...  

Persistent pulmonary hypertension is a very rare presentation of congenital virus infection. We discuss the case of complete congenital rubella syndrome presenting at echocardiography with pulmonary hypertension that worsened after ductus ligation. Cardiac catheterization showed a normal pulmonary valve and vascular tree but aPAP=40 mmHg. The infant promptly responded to inhaled nitric oxide while on mechanical ventilation and was later shifted to oral sildenafil. It is not clear whether our observation may be due to direct viral damage to the endothelium or to the rubella virus increasing the vascular tone via a metabolic derangement.


Cureus ◽  
2021 ◽  
Author(s):  
Mubashar Iqbal ◽  
Hira Yousuf ◽  
Zara Majeed ◽  
Muhammad Zohaib ◽  
Ashish Mishra ◽  
...  

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