scholarly journals Solitary Fibrous Tumor of the Floor of the Mouth: Case Report and Review of the Literature

2006 ◽  
Vol 85 (7) ◽  
pp. 437-439 ◽  
Author(s):  
Neville Shine ◽  
Mohd nor nurul Khasri ◽  
Jim Fitzgibbon ◽  
Gerard O'Leary
2008 ◽  
Vol 14 (2) ◽  
pp. 213-217 ◽  
Author(s):  
Giuseppe Leoncini ◽  
Vincenza Maio ◽  
Marco Puccioni ◽  
Alessandro Franchi ◽  
Vincenzo De Giorgi ◽  
...  

2006 ◽  
Vol 130 (2) ◽  
pp. 213-216 ◽  
Author(s):  
Jorge E. Dotto ◽  
William Ahrens ◽  
David J. Lesnik ◽  
Diane Kowalski ◽  
Clarence Sasaki ◽  
...  

Abstract Solitary fibrous tumors are relatively rare mesenchymal neoplasms that were originally described as pleural- or peritoneal-based lesions. Although they were considered a form of mesothelioma, subsequent investigation failed to reveal mesothelial differentiation. Characterization of their histologic and immunohistochemical features, as well as identification in a multitude of nonmesothelial-based locations has further served to distinguish these lesions from the more diffuse and aggressive mesothelioma. Reports of solitary fibrous tumor in the larynx are extremely rare. We report a case of solitary fibrous tumor of the larynx in a 38-year-old man.


2019 ◽  
Vol 13 (1) ◽  
Author(s):  
Hailu Wondimu Gebresellassie ◽  
Yusuf Mohammed ◽  
Brahenu Kotiso ◽  
Bereket Amare ◽  
Aemero Kebede

1996 ◽  
Vol 75 (10) ◽  
pp. 681-684 ◽  
Author(s):  
Kunal Gangopadhyay ◽  
Khalid Taibah ◽  
M. Babu Manohar ◽  
Hala Kfoury

Solitary fibrous tumors are uncommon spindle cell neoplasms generally associated with serosal surfaces, especially the pleura. Recently, these tumors have been documented in a number of extrapleural sites including the head and neck. So far only two cases of parapharyngeal solitary fibrous tumor have been reported in the English literature. Rare location of an uncommon lesion often gives rise to difficulty in diagnosis or to misdiagnosis. In both the previously reported cases, as well as in our case, the diagnosis of solitary fibrous tumor was not made until the excised tumor was subjected to histopathology and immunohistochemistry.


2014 ◽  
Vol 3 (4) ◽  
pp. 215-219
Author(s):  
Masayuki Sano ◽  
Mayuko Tokunaga ◽  
Shinichiro Murayama ◽  
Shizue Nyomura ◽  
Taro Murata ◽  
...  

2010 ◽  
Vol 76 (2) ◽  
pp. e39-e42
Author(s):  
Wanling Ma ◽  
Hong Yin ◽  
Yi Huan ◽  
Cheng Ma ◽  
Yuqiao Xu ◽  
...  

2004 ◽  
Vol 7 (6) ◽  
pp. 653-660 ◽  
Author(s):  
Dinesh Rakheja ◽  
Kathleen S. Wilson ◽  
John J. Meehan ◽  
Roger A. Schultz ◽  
Gerhard E. Maale ◽  
...  

We report a case of a benign solitary fibrous tumor that occurred in the right shoulder of a 9-year-old girl. This case is remarkable due to the unusual location of its occurrence and the young age of the patient. In addition, cytogenetic analysis revealed a karyotype unreported in this neoplasm: 46,XX,der(4)t(4;9)(q31.1;q34), del(9)(p22p24),der(9)t(4;9)(q31.1;q34)ins(9;?)(q34;?) (17 cells)/46,XX (3 cells).


2005 ◽  
Vol 32 (3) ◽  
pp. 285-289 ◽  
Author(s):  
Tsugio Abe ◽  
Atushi Murakami ◽  
Tsuneo Inoue ◽  
Shigenori Ohde ◽  
Takehiko Yamaguchi ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document