Download full-text PDF |
Source |
|---|---|
| http://dx.doi.org/10.1016/0300-9572(89)90018-x | DOI Listing |
Publication Analysis
Top Keywords
Similar Publications
Surgical Excision of Pulmonary Metastases of Dermatofibrosarcoma Protuberans.
Cureus
October 2024
Thoracic Surgery, Fondazione Policlinico Universitario "Agostino Gemelli" IRCCS, Università Cattolica del Sacro Cuore, Roma, ITA.
Dermatofibrosarcoma protuberans (DFSP) is a rare malignancy of mesenchymal origin of medium-low grade with a tendency to local recurrences but not to distant metastases. We present the case of a 37-year-old male who underwent surgical resection of a 1.2 cm DFSP lesion on the left shoulder in May 2020.
View Article and Find Full Text PDFOrbital solitary fibrous tumor.
J Fr Ophtalmol
November 2024
Ophthalmology 2, CHNO 15-20, Sorbonne University, 55bis, boulevard du Montparnasse, 75006 Paris, France.
Introduction: 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.
Case Description: 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 diplopia. The diagnoses relied on histopathological analysis of biopsy samples.
Solitary fibrous tumour is a relatively rare soft tissue fibroblastic tumour, accounting for approximately 2% of soft tissue tumours. It has been described primarily as a tumour of the pleural cavity; however, up to 70% of cases occur elsewhere, in any anatomical location, which can make diagnosis difficult. If this is the diagnosis being considered, the STAT6 antibody is currently available with high sensitivity and specificity.
View Article and Find Full Text PDFTotal management of hemangiopericytoma/solitary fibrous tumor of the buttock: A case report.
Medicine (Baltimore)
July 2024
Department of Orthopedic Surgery, Kindai University Hospital, Osaka-Sayama City, Osaka, Japan.
Background: Solitary fibrous tumors can manifest at various anatomical sites, predominantly occurring at extrapleural sites with a peak incidence between 40 and 70 years. SFT necessitates long-term follow-up owing to its tumor characteristics. However, comprehensive reports covering the period from initial diagnosis to the patient's demise are lacking.
View Article and Find Full Text PDFMalignant solitary fibrous tumor of the kidney with IGF2 secretion and without hypoglycemia.
World J Surg Oncol
July 2024
Department of Pathology, Shanghai Jiaotong University Medical School Affiliated Ruijin Hospital, Number 197, Ruijin Er Road, Huangpu District, Shanghai, China.
Background: Solitary fibrous tumor (SFT) is a rare fibroblastic mesenchymal tumor that mostly involves the pleura and infrequently involves extra-pleural sites. De novo SFT of the kidney is uncommon, and malignant SFT is extremely rare.
Case Presentation: We report a case of a 51-year-old man with a large malignant SFT in the left kidney.
Want AI Summaries of new PubMed Abstracts delivered to your In-box?
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!