scholarly journals A rare case of low-grade fibromyxoid sarcoma with ossification which was radiologically detected as apparent calcification and histopathologically proven

2018 ◽  
Vol 12 ◽  
pp. 24-28
Author(s):  
Yasuaki Tsuchida ◽  
Yoshitane Tsukamoto ◽  
Hiroyuki Futani ◽  
Shunsuke Kumanishi ◽  
Takahiro Watanabe ◽  
...  
2020 ◽  
Vol 8 ◽  
pp. 2050313X2094431
Author(s):  
Diandra Perez ◽  
Ola El-Zammar ◽  
Brando Cobanov ◽  
Rana Naous

Low-grade fibromyxoid sarcoma, also known as Evans tumor, is a low-grade sarcoma that most commonly arises in the deep soft tissue of the proximal extremities or trunk in young adults. It is very rare in the viscera as a primary site, with only a few cases reported in the literature. Here, we present a case of Evans tumor occurring in an unusual and rarely reported location; an intrathoracic mass arising from the diaphragmatic pleura.


2014 ◽  
Vol 7 (4) ◽  
pp. 1308-1312 ◽  
Author(s):  
JEETENDRA BAJPAI ◽  
SAURAV SHUKLA ◽  
MOAZZAM JAH ◽  
ALOK KUMAR SINGH ◽  
MOHIT GOEL ◽  
...  

Author(s):  
Agnieszka Niepokój-Czopnik ◽  
Michał Aporowicz ◽  
Łukasz Hałoń ◽  
Adam Maciejczyk ◽  
Rafał Matkowski

2015 ◽  
Vol 71 (S1) ◽  
pp. 25-26
Author(s):  
T. Kanato ◽  
S. Kalyani ◽  
T. Lailyang ◽  
D. Santosh ◽  
T. Rebecca ◽  
...  

2021 ◽  
Vol 12 (2) ◽  
pp. 271
Author(s):  
VinayakGourish Naik ◽  
KirthiKumar Rai ◽  
HR Shivakumar

2009 ◽  
Vol 27 (9) ◽  
pp. 375-380 ◽  
Author(s):  
Eriko Maeda ◽  
Satoshi Ohta ◽  
Takeyuki Watadani ◽  
Akiteru Goto ◽  
Atsushi Nakajima ◽  
...  

2006 ◽  
Vol 130 (9) ◽  
pp. 1358-1360 ◽  
Author(s):  
Stephen E. Vernon ◽  
Pablo A. Bejarano

Abstract Low-grade fibromyxoid sarcomas are uncommon deep soft tissue neoplasms first described by Evans in 1987. They exhibit a deceptively benign appearance, with a whorled or linear arrangement of spindle-shaped cells showing few to absent mitoses. A characteristic, but not specific, feature is the presence of areas of myxoid stroma. Recurrences are common, and late metastases have been recorded. A closely related but morphologically distinct tumor, the so-called hyalinizing spindle cell tumor with giant rosettes, has also been described; both neoplasms share the same cytogenetic abnormality, a balanced translocation resulting in a FUS/CREB3L2 fusion gene. Because of similar clinical behavior and the common cytogenetic abnormality, some authors prefer to consider both lesions as a single entity within the spectrum of low-grade sarcomas.


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