Treatment of orbital solitary fibrous tumour with gamma knife radiosurgery and systematic review of literature

Tata, A.; Cohen-Inbar, Or; Sheehan, Jason P.

doi:10.1136/bcr-2016-217114

Cited by 15 publications

(8 citation statements)

References 22 publications

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“…Ra dio ther a py may be indicated if SFTs are suspected to be malignant or margin-positive. However, opinions regarding radiotherapy efficacy vary 12,13 .…”

Section: Discussionmentioning

confidence: 99%

Solitary fibrous tumor of the buccal mucosa: A case report

Yamaguchi

Takamatsu

Kurasawa

et al. 2023

Showa Univ J Med Sci

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Solitary fibrous tumors (SFTs) were reported in 1931 as tumors derived from mesenchymal tissue. They occur mainly in the pleura and peritoneum and rarely in the oral and maxillary regions. This report presents the case of a 48-year-old woman with a tumor in the left buccal mucosa. We suspected a salivary gland tumor or hemangioma. Excision was performed under general anesthesia. The lesion was removed as a single mass. Histopathological and immunohistochemical analyses led to the diagnosis of SFT. We report this case based on a literature review.

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“…Ra dio ther a py may be indicated if SFTs are suspected to be malignant or margin-positive. However, opinions regarding radiotherapy efficacy vary 12,13 .…”

Section: Discussionmentioning

confidence: 99%

Solitary fibrous tumor of the buccal mucosa: A case report

Yamaguchi

Takamatsu

Kurasawa

et al. 2023

Showa Univ J Med Sci

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“…Extrapleural SFTs are almost always benign and cured by means of simple surgical excision (13). Stereotactic radiosurgery was treatment option in for recurrent solitary fibrous tumour and for patient refused surgery, percutaneous thermal ablation was proposed as a treatment alternative which can prevent surgical scar, reduced recovery time (14). The SFT affecting the patient was located in the buccal space, extended into the infratemporal space (Fig.…”

Section: Discussionmentioning

confidence: 99%

Transoral surgical approach to solitary fibrous tumors in buccal space with infratemporal tumor extension: A case report

Rizqiawan¹,

Zahratur-Rasyida²,

Mulyawan³

2020

J Clin Exp Dent

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A solitary fibrous tumour (SFT) is a rare spindle-cell neoplasm of mesenchymal origin usually located in the pleura. It has been recently described as occurring in various head and neck sites, including the oral cavity. The purpose of this article is to report a case of SFT originating in the buccal space and extending into the infratemporal space treated by means of transoral approach surgery. A 25-year-old female patient reported to the Department of Oral and Maxillofacial Surgery, Universitas Airlangga Hospital, chiefly complaining of a painless lump in the left cheek which had been present for nine months. The diagnosis was arrived at on the basis of a combination of clinical investigation, imaging studies and histopathological examination (biopsy). The surgical approach involved transoral incision through the buccal mucosa. An SFT of buccal space may extend to nearby structures producing the anatomical challenge of removal through a transoral approach. Excisional biopsy involving a transoral approach is, nevertheless, considered appropriate because it produces an attractive aesthetic appearance, reduces morbidity from nerve/ vascular/ gland injury and promotes more effective healing.

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“…2 Development of multiple orbital SFTs is extremely rare, and there had been only 2 reported cases. 5,6 Here, we report a pediatric case of 2 adjacent CD34-negative orbital SFTs.…”

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confidence: 91%

Multiple CD34-Negative Orbital Solitary Fibrous Tumors in a Pediatric Patient

Someda,

Miyazaki,

Takahashi

2023

Ophthalmic Plastic &Amp; Reconstructive Surgery

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A 12-year-old Japanese male presented with a 2-month history of headache that was later on associated with diplopia, painless proptosis of the OS, and left ophthalmoplegia. Initial examination revealed a 7-mm OS protrusion, which worsened to 9 mm in less than a month. Preoperative visual acuity worsened from 1.0 to 0.2 with the development of left afferent pupillary defect. Left ocular motility was severely restricted in all directions. Magnetic resonance imaging showed two well-defined lesions adjacent to one another in the left orbit. The patient underwent surgical excision of the left orbital masses. Histopathology findings were consistent with solitary fibrous tumor of the orbit. Immunohistochemistry findings revealed CD34-negative but signal transducer and activator of transcription 6-positive for both specimens. The patient was monitored postoperatively and there was no recurrence of the tumor even after 6 months.

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Treatment of orbital solitary fibrous tumour with gamma knife radiosurgery and systematic review of literature

Cited by 15 publications

References 22 publications

Solitary fibrous tumor of the buccal mucosa: A case report

Solitary fibrous tumor of the buccal mucosa: A case report

Transoral surgical approach to solitary fibrous tumors in buccal space with infratemporal tumor extension: A case report

Multiple CD34-Negative Orbital Solitary Fibrous Tumors in a Pediatric Patient

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