Results 261 to 270 of about 71,140 (312)

STAT6 Expression in Solitary Fibrous Tumor and Histologic Mimics: a Single Institution Experience

Applied immunohistochemistry & molecular morphology (Print), 2020
STAT6 stain has proved to be a good surrogate marker for the genetic alteration (NAB2-STAT6 gene fusion) in solitary fibrous tumor (SFT). This study aims to validate the use of STAT6 rabbit monoclonal antibody in differentiating SFT from its histologic ...
Omer A M Saeed, Shanxiang Zhang, Liang Cheng, Jingmei Lin, Fatimah I. Alruwaii, Shaoxiong Chen   +5 more
semanticscholar   +1 more source

Orbital solitary fibrous tumor

Journal Français d'Ophtalmologie
Solitary fibrous tumor (SFT) is a rare borderline mesenchymal tumor typically arising in the pleura and involving the orbit as its most common extra-pleural location.We herein describe two cases of orbital SFT arising in both a 69-year-old woman presenting with progressive proptosis of the left eye and a 49-year-old woman presenting with binocular ...
B. Paganelli, J. Meney, J.-P. Nordmann, A. Bennedjaï   +3 more
openaire   +2 more sources

Solitary Fibrous Tumors

2012
Solitary fibrous tumors (SFT) are rare mesenchymal tumors that can affect central nervous system at any level. Histologically, they are characterized by round to spindle-shaped fibroblastic cells set in a collagenous matrix with variable amounts of hyalinized collagen bundles and strongly positive stain for CD34 on immunohistochemistry.
Guilherme Geib, Tania W. Furlanetto
openaire   +1 more source

Solitary Fibrous Tumors

DeckerMed CGSO Case-Based Reviews, 2018
Solitary fibrous tumors (SFTs) are a subtype of soft tissue sarcoma with fibroblastic differentiation. SFTs typically occur in patients between ages 50 and 70 and most commonly develop in the pleural space or abdomen, although they have been described in virtually every body site.
Stephen F Sener, Lawrence R Menendez, James S Hu, Omar Ragab, Gino K In, Dakshesh Patel, Shefali Chopra, William W Tseng   +7 more
openaire   +1 more source

Superficial Solitary Fibrous Tumor: A Series of 26 Cases

American Journal of Surgical Pathology, 2018
While superficial (cutaneous/subcutaneous) solitary fibrous tumor (SFT) have been described, definitive diagnosis is difficult due to overlapping features with other tumors. We describe the largest series to date of superficial SFT.
P. Feasel, A. Al-Ibraheemi, K. Fritchie, R. Zreik, Wei-Lien Wang, Elizabeth G. Demicco, M. Saeb-Lima, J. Goldblum, B. Rubin, J. McKenney, J. Ko, S. Billings   +11 more
semanticscholar   +1 more source

Solitary fibrous tumor of parotid gland: a case report and short review of literature.

European Review for Medical and Pharmacological Sciences, 2022
F. Goker, C. Mazzucato, M. Maggioni, A. Baj, A. Giannì, G. Beltramini, A. Russillo, F. R. Buccellato, D. Rossi, C. Mortellaro, M. Del Fabbro   +10 more
semanticscholar   +1 more source

Toward Better Understanding and Management of Solitary Fibrous Tumor.

Surgical Oncology Clinics of North America, 2022
K. Kazazian, Elizabeth G. Demicco, M. de Perrot, D. Strauss, C. Swallow   +4 more
semanticscholar   +1 more source

Mediastinal solitary fibrous tumor

Cirugía Española (English Edition), 2022
Ana, Triviño, Inmaculada, Sabariego, Manuel, Pérez-Pérez, Rafael, Jiménez Merchán   +3 more
openaire   +2 more sources

Pericardial Solitary Fibrous Tumor on FDG PET/CT.

Clinical Nuclear Medicine, 2019
Solitary fibrous tumor, which can occur in all parts of the body and is more frequently found in the visceral pleura, is a rare mesenchymal tissue-originating spindle cell tumor derived from CD34-positive dendriticmesenchymal cells, but it rarely occurs ...
Dan Shao, Shu-xia Wang
semanticscholar   +1 more source

Solitary fibrous tumor.

The Annals of otology, rhinology, and laryngology, 1993
First described as a pleural neoplasm, the solitary fibrous tumor has been reported in a number of extrapleural sites, including the upper respiratory tract. The neoplasm is of mesenchymal origin, exists in benign and malignant forms, and is a histopathologic diagnosis made after exclusion of other soft tissue neoplasms.
J G, Batsakis, R D, Hybels, A K, el-Naggar   +2 more
openaire   +1 more source