Pulmonary Artery Intimal Sarcoma Mimicking Pulmonary Thromboembolism

Author(s):  
Gokhan Celik ◽  
Aydin Ciledag ◽  
Cabir Yuksel ◽  
Bulent M. Yenigun ◽  
Hakan Kutlay ◽  
...  
2019 ◽  
Vol 58 (24) ◽  
pp. 3599-3600
Author(s):  
Konomi Sennari ◽  
Kei Yamasaki ◽  
Fumihiro Tanaka ◽  
Kazuhiro Yatera

Medicine ◽  
2021 ◽  
Vol 100 (6) ◽  
pp. e24699
Author(s):  
Ying-Chun Li ◽  
Le-Yao Li ◽  
Hai-Chao Tong ◽  
Hong-Tao Xu ◽  
Shuang Ma ◽  
...  

2014 ◽  
Vol 20 (10) ◽  
pp. S159
Author(s):  
Hiromi Tsuchiya ◽  
Takashi Yanagisawa ◽  
Masayuki Ogiwara ◽  
Hikaru Kimura ◽  
Miki Horigome ◽  
...  

2020 ◽  
Vol 66 (1) ◽  
pp. 403-406
Author(s):  
Reisha Rijal ◽  
Asit Ranjan Mridha ◽  
Sudheer Kumar Arava ◽  
Chittaranjan Behera

Haigan ◽  
2017 ◽  
Vol 57 (7) ◽  
pp. 875-876
Author(s):  
Yohei Kawaguchi ◽  
Tetsuya Okano ◽  
Masatoshi Kakihana ◽  
Naohiro Kajiwara ◽  
Tatsuo Ohira ◽  
...  

2021 ◽  
Vol 2021 ◽  
pp. 1-4
Author(s):  
Daiki Kato ◽  
Shohei Mori ◽  
Eriko Harada ◽  
Rintaro Shigemori ◽  
Takamasa Shibazaki ◽  
...  

Introduction. Intimal sarcoma is a very rare tumor arising within the intima of the pulmonary artery. Preoperative diagnosis of pulmonary artery sarcoma is difficult, and the tumor is sometimes misdiagnosed as pulmonary thromboembolism. We report a case of pulmonary artery intimal sarcoma successfully diagnosed by preoperative endovascular biopsy and treated via right pneumonectomy and pulmonary arterioplasty. Presentation of a Case. A 72-year-old woman was referred to our hospital with a low-attenuation defect in the lumen of the right main pulmonary artery by computed tomography. Pulmonary artery thromboembolism was suspected, and anticoagulation therapy was administered. However, the defect in the pulmonary artery did not improve. Endovascular catheter aspiration biopsy was performed. Histological examination revealed pulmonary artery sarcoma. The patient was treated with right pneumonectomy and arterioplasty with the use of cardiopulmonary bypass. Discussion. Preoperative biopsy by endovascular catheter is worth considering for a patient with a tumor in the pulmonary artery and can help in planning treatment strategies.


2010 ◽  
Vol 25 (1) ◽  
pp. 29-31 ◽  
Author(s):  
Yulong Hou ◽  
Zhenya Shen ◽  
Wei Gao ◽  
Wenxue Ye

2013 ◽  
Vol 2013 ◽  
pp. 1-3 ◽  
Author(s):  
Hazel Villanueva ◽  
Sandeepkumar Kuril ◽  
Jennifer Krajewski ◽  
Aziza Sedrak

Introduction. Sickle cell hemoglobin D disease (HbSD) is a rare variant of sickle cell disease (SCD). Incidence of pulmonary thromboembolism (PE) and deep venous thrombosis (DVT) in children with HbSD is unknown. PE and DVT are known complications of SCD in adults but have not been reported in the literature in children with HbSD.Case Report. We are reporting a case of a 12-year-old boy with HbSD with acute chest syndrome (ACS) complicated by complete thrombosis of the branch of the right pulmonary artery and multiple small pulmonary artery emboli seen on computed tomography (CT) pulmonary angiogram and thrombosis of the right brachial vein seen on Doppler ultrasound. Our patient responded to treatment with anticoagulant therapy.Conclusion. There are no cases reported in children with HbSD disease presenting as ACS with pulmonary thromboembolism. We suggest that PE should be suspected in patients presenting with ACS who do not show improvement with standard management. CT pulmonary angiogram should be utilized for early diagnosis and appropriate management as there is no current protocol for management of PE/DVT in pediatric patients with SCD.


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