ALLMedicine™ Solitary Fibrous Tumor Center
Research & Reviews 969 results
https://doi.org/10.1016/j.wneu.2021.02.026
World Neurosurgery; Gopakumar S, Srinivasan VM et. al.
Feb 20th, 2021 - Intracranial solitary fibrous tumors (ISFTs) are rare neoplasms of mesenchymal origin that originate from the meninges. ISFTs of the skull base can be challenging to treat as resection can be complicated by skull base anatomy. We present two cases...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7893919
BMC Surgery; Wang X, Shen J et. al.
Feb 19th, 2021 - Orbital solitary fibrous tumors (SFTs) are rare neoplasms. Recurrent, hypervascular, malignant variations of orbital SFTs have recently been noted and can present a surgical challenge. We describe a case of a 53-year-old Chinese woman with a histo...
https://doi.org/10.1177/0145561321991338
Ear, Nose, & Throat Journal; Xu M, Chen M et. al.
Feb 3rd, 2021 - Solitary fibrous tumor/hemangiopericytoma (SFT/HPC) is extremely rare, and most of them are immediately treated for radical resection. However, the information concerning its natural history remains unclear. In this report, we presented a patient ...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7871082
The Journal of International Medical Research; Qin J, Zhu Y et. al.
Feb 3rd, 2021 - Solitary fibrous tumor (SFT) is a rare soft tissue neoplasm of mesenchymal origin. SFT is most commonly located in the thoracic cavity (in approximately 80% of cases), but can also develop rarely in the pelvis. A 47-year-old man presented to our h...
https://doi.org/10.1111/tbj.14175
The Breast Journal; Nitta T, Kimura K et. al.
Jan 29th, 2021 - Malignant solitary fibrous tumor of the breast.|2021|Nitta T,Kimura K,Tominaga T,Ikari A,Takashima Y,|
Clinicaltrials.gov 973 results
https://doi.org/10.1016/j.wneu.2021.02.026
World Neurosurgery; Gopakumar S, Srinivasan VM et. al.
Feb 20th, 2021 - Intracranial solitary fibrous tumors (ISFTs) are rare neoplasms of mesenchymal origin that originate from the meninges. ISFTs of the skull base can be challenging to treat as resection can be complicated by skull base anatomy. We present two cases...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7893919
BMC Surgery; Wang X, Shen J et. al.
Feb 19th, 2021 - Orbital solitary fibrous tumors (SFTs) are rare neoplasms. Recurrent, hypervascular, malignant variations of orbital SFTs have recently been noted and can present a surgical challenge. We describe a case of a 53-year-old Chinese woman with a histo...
https://doi.org/10.1177/0145561321991338
Ear, Nose, & Throat Journal; Xu M, Chen M et. al.
Feb 3rd, 2021 - Solitary fibrous tumor/hemangiopericytoma (SFT/HPC) is extremely rare, and most of them are immediately treated for radical resection. However, the information concerning its natural history remains unclear. In this report, we presented a patient ...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7871082
The Journal of International Medical Research; Qin J, Zhu Y et. al.
Feb 3rd, 2021 - Solitary fibrous tumor (SFT) is a rare soft tissue neoplasm of mesenchymal origin. SFT is most commonly located in the thoracic cavity (in approximately 80% of cases), but can also develop rarely in the pelvis. A 47-year-old man presented to our h...
https://doi.org/10.1111/tbj.14175
The Breast Journal; Nitta T, Kimura K et. al.
Jan 29th, 2021 - Malignant solitary fibrous tumor of the breast.|2021|Nitta T,Kimura K,Tominaga T,Ikari A,Takashima Y,|
News 2 results
https://www.mdedge.com/dermatology/article/151057/dermatopathology/solitary-tender-nodule-back
Claire O. Dorfman, DO, Christian W. Oram, DO et. al.
Nov 3rd, 2017 - The Diagnosis: Solitary Fibrous Tumor Solitary fibrous tumors (SFTs), as first described by Klemperer and Rabin1 in 1931, are relatively uncommon mesenchymal neoplasms that occur primarily in the pleura. This lesion is now known to affect many oth.
https://www.mdedge.com/hematology-oncology/article/102189/gastroenterology/life-threatening-hypoglycemia-resulting-nonislet
Nirosshan Thiruchelvam et al
Aug 25th, 2015 - Nonislet cell tumor-induced hypoglycemia (NICTH), also known as Doege-Potter syndrome, is a rare paraneoplastic syndrome seen in association with various nonpancreatic tumors, benign and malignant, and comprising mesenchymal, vascular, or epitheli.