scholarly journals Pulmonary Hypertension Caused by Lung Cancer Suspected to Have Pulmonary Tumor Thrombotic Microangiopathy and Which We Treated with Gefitinib

Haigan ◽  
2012 ◽  
Vol 52 (4) ◽  
pp. 420-425 ◽  
Author(s):  
Kiyokazu Yoshinoya ◽  
Yu Kasamatsu ◽  
Shougen Boku ◽  
Takashi Kida ◽  
Masatoshi Kadoya ◽  
...  
2021 ◽  
Vol 3 (7) ◽  
pp. 1029-1031
Author(s):  
Benjamin P. Schwartz ◽  
Philip Tracy ◽  
Stephanie Hon ◽  
Harrison W. Farber ◽  
James E. Udelson

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.


2021 ◽  
Author(s):  
Ryo Kamidani ◽  
Keisuke Kumada ◽  
Hideshi Okada ◽  
Genki Yoshimura ◽  
Tomohiro Kanayama ◽  
...  

Abstract Background: Pulmonary tumor thrombotic microangiopathy (PTTM) is a condition that involves the development of pulmonary hypertension due to the presence of microscopic tumor emboli of the peripheral pulmonary arteries. Here, we report a case of rapidly exacerbating PTTM associated with gastric cancer that was identified postmortem through pathological autopsy.Case presentation: A 52-year-old Asian woman who experienced anterior chest pain while coughing visited the orthopedic department of the Gifu University Hospital. She was diagnosed as having multiple osteolytic bone metastases throughout her body and was subsequently scheduled to undergo combined positron emission tomography and computed tomography (CT) to search for a primary lesion. However, 4 days after her visit to the orthopedic department, she was unable to stand up and thus visited the emergency department. At the time of admission, physical examination results revealed that she had a percutaneous oxygen saturation level of 90% (on room air) and cyanosis, and that she was in a state of hemodynamic shock. Laboratory test results revealed elevated levels of fibrin degradation products and D-dimer in her blood. Chest CT results were normal. She was admitted to the hospital’s general ward for follow-up but soon entered a gradually worsening state of shock and respiratory failure. Electrocardiography revealed findings associated with right heart strain; however, contrast-enhanced CT did not reveal the presence of pulmonary embolism. She was admitted to the intensive care unit and was treated for pulmonary hypertension; however, 45 h after her arrival at the hospital, she died of respiratory failure. A pathological autopsy revealed the presence of gastric cancer, tumor microemboli, and fibrous intimal thickening of the peripheral arteries of both lungs; thus, a diagnosis of PTTM was made. Conclusions: In patients with carcinoma of unknown primary site and pulmonary hypertension with pulmonary embolism ruled out by CT, emergency physicians and intensivists must consider the possibility of PTTM, which represents an oncologic emergency, and initiate chemotherapy administration as soon as possible.


Cancer ◽  
1990 ◽  
Vol 66 (3) ◽  
pp. 587-592 ◽  
Author(s):  
Axel von Herbay ◽  
Annemarie Illes ◽  
Rüdiger Waldherr ◽  
Herwart F. Otto

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