extraosseous osteosarcoma
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2020 ◽  
Vol 21 (1) ◽  
Author(s):  
Tiantian Wang ◽  
Shijie Liao ◽  
Xiaofei Ding ◽  
K. C. Anil ◽  
Qian Huang ◽  
...  

2017 ◽  
pp. bcr-2017-219722 ◽  
Author(s):  
Muhammad Furrukh ◽  
Asim Qureshi ◽  
Nadira Mamoon ◽  
Menahil Fatima

2017 ◽  
Vol 75 (3) ◽  
pp. 650.e1-650.e5
Author(s):  
Andro Košec ◽  
Majda Vučić ◽  
Vladimir Bedeković ◽  
Mirko Ivkić

2016 ◽  
Vol 21 (2) ◽  
pp. 103
Author(s):  
A Adeyemo ◽  
A.O. Komolafe ◽  
S.A. Ameye ◽  
A.M. Owojuyigbe ◽  
A.O. Olakanmi ◽  
...  

2016 ◽  
Vol 41 (8) ◽  
pp. 650-653 ◽  
Author(s):  
Lei Jiang ◽  
Lijuan Luan ◽  
Hong Yun ◽  
Yingyong Hou ◽  
Hongcheng Shi

2016 ◽  
Vol 7 (4) ◽  
pp. 464-466
Author(s):  
Anish P. Nagpal ◽  
Somesh Chandra ◽  
Shaifali Goel

2016 ◽  
Vol 01 (01) ◽  
Author(s):  
Xiang Salim ◽  
David Paton ◽  
Anton Lambers ◽  
Richard Carey Smith

2016 ◽  
Vol 9 ◽  
pp. CCRep.S38384 ◽  
Author(s):  
Tsering Gyalpo Lama Tamang ◽  
Marina Shuster ◽  
Abhinav B. Chandra

Introduction Extraosseous osteosarcomas are rare, accounting for approximately 4% of all osteosarcomas. A literature review yields very few cases of osteosarcoma primarily arising from the hepatic parenchyma. Case Report This report describes a case of a man in his 50s with a history of hepatitis C and cirrhosis who presented with 5 days of progressive right upper quadrant pain. Magnetic resonance imaging of the abdomen and pelvis demonstrated a 4.4 cm X 4.8 cm X 4.8 cm right hepatic lobe mass with a large area of necrosis and peripheral enhancement. The subsequent liver biopsy showed few cores of tumor composed of fibroblastic malignant cells producing lace-like osteoid matrix. Osteosarcomatous foci in other parts of the body were excluded by performing extensive physical examination, radiologic imaging, and biopsy. Hence, a primary osteosarcoma was diagnosed. The patient underwent portal vein embolization in preparation for a surgical resection of the right liver lobe. He was admitted six weeks after the embolization for dyspnea and abdominal distension and expired due to abdominal hematoma and pulmonary embolism. Conclusion Based on the rarity, lack of consensus in treatment, and dismal prognosis, extraosseous osteosarcoma should be considered a separate entity from osseous osteosarcoma. More data and research are needed in this rare and understudied malignancy.


2015 ◽  
Vol 473 (11) ◽  
pp. 3604-3611 ◽  
Author(s):  
Zhengfu Fan ◽  
Shreyaskumar Patel ◽  
Valerae O. Lewis ◽  
B. Ashleigh Guadagnolo ◽  
Patrick P. Lin

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