scholarly journals 261 Invasive Pulmonary Artery Intimal Sarcoma: A Rare Case of an Aggressive Tumor With Extended Survival

2018 ◽  
Vol 149 (suppl_1) ◽  
pp. S111-S111
Author(s):  
Stacey Reed ◽  
Edward Lynch ◽  
Jan Silverman
2019 ◽  
Vol 28 ◽  
pp. S109
Author(s):  
Damian Gimpel ◽  
Timothy Oh ◽  
David J. Mccormack ◽  
Nick Odom ◽  
Zaw Lin

2021 ◽  
Vol 49 (1) ◽  
pp. 030006052098465
Author(s):  
Mingyue Cui ◽  
Binfeng Xia ◽  
Heru Wang ◽  
Haihui Liu ◽  
Xia Yin

Aortopulmonary window is a rare congenital heart disease that can increase pulmonary vascular resistance, exacerbate left-to-right shunt and lead to heart failure and respiratory tract infections. Most patients die during childhood. We report a 53-year-old male patient with a large aortopulmonary window combined with anomalous origin of the right pulmonary artery from the aorta, with Eisenmenger syndrome and without surgery.


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

CASE ◽  
2021 ◽  
Author(s):  
Tamami Nakagawa-Kamiya ◽  
Mika Mori ◽  
Miho Ohira ◽  
Kenji Iino ◽  
Masa-aki Kawashiri ◽  
...  

2018 ◽  
Vol 66 (3) ◽  
pp. 268-270
Author(s):  
Ersin Günay ◽  
Furkan Kaya ◽  
Sibel Günay

2021 ◽  
Author(s):  
Xiaofang Bai ◽  
Litao Ruan

Abstract Background: Pulmonary artery intimal sarcoma(PAS) is a very rare disease, the prevalence of it is about 0.001%-0.003%1. PAS is often misdiagnosed as acute or chronic pulmonary thromboembolism due to its clinical presentation and radiological findings. Thus early diagnosis is very crucial and may improve patient outcome.Case presentation: Here we report a case in a Chinese male which the symptom as presentation was episodes of shortness of breath. Transthoracic echocardiography showed a solid mass in the pulmonary valve orifice, which was demonstrated to be a pulmonary artery intimal sarcoma diagnosed by histopathology2. In this case the initial differential diagnosis included pulmonary embolism. Because the initial symptom of primary pulmonary artery sarcoma is extremely similiar to the pulmonary embolism. Half of them may be misdiagnosed as pulmonary embolism. Imaging studies are very helpful. Ultrasound and CT are the best due to their resolution and ability to assess the relationship of the mass with the surrounding structures. The final diagnosis is mostly made after surgical excision and this is the most effective treatment. At the same time, radiotherapy and chemotherapy after surgery is also a adjuvant treatment3.Conclusion: We report a very rare case of pulmonary artery intimal sarcoma, due to late diagnosis and delayed treatment in this case, the patient display a poor prognostic. Early diagnosis and right treatment can improve the prognosis of PAS and optimize overall health.


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