Solitary fibrous tumor of the lacrimal sac: A rare entity and a brief review of the literature

2021 ◽  
Vol 1 (4) ◽  
pp. 731
Author(s):  
Deepsekhar Das ◽  
Sahil Agrawal ◽  
Aishwarya Rathod ◽  
Sujeeth Modaboyina ◽  
Seema Sen ◽  
...  
Keyword(s):  
Solitary Fibrous Tumor ◽  
Rare Entity ◽  
Review Of The Literature ◽  
Lacrimal Sac ◽  
Fibrous Tumor

scholarly journals Recurrent Solitary Fibrous Tumor in Intradural Extramedullary Space: Case Report and Review of the Literature

2021 ◽  
Vol 2021 ◽  
pp. 1-14
Author(s):  
Neris Dincer ◽  
Melisa Bagci ◽  
Metin Figen ◽  
Adem Yilmaz ◽  
Ahmet Mesrur Halefoglu ◽  
...  
Keyword(s):  
Solitary Fibrous Tumor ◽  
Case Reports ◽  
Treatment Algorithm ◽  
Surgical Excision ◽  
Rare Entity ◽  
Review Of The Literature ◽  
Patient Reported ◽  
Intradural Extramedullary ◽  
Fibrous Tumor ◽  
Space Case

Solitary fibrous tumor/hemangiopericytoma (SFT/HPC) is a rare neoplasm arising from spindle cells and most commonly arising from pleura. Spinal SFT/HPC is a rare entity; hence, it is not on the top of the differential diagnosis list when a clinician faces a spinal lesion. In the review of the literature, there exist less than 50 case reports of intradural extramedullary SFT/HPC. Here, we present a 54-year-old female patient who underwent subtotal surgical excision of an intradural extramedullary spinal mass pathologically reported to be SFT/HPC and had symptomatic recurrence in the 3rd year of follow-up. Surgical intervention was unachievable and the patient was given 45 Gy to the surgical cavity followed by a 5.4 Gy boost to visible tumor with external radiotherapy. Patient reported significant relief of her symptoms. We aim to contribute to the formation of a treatment algorithm for this rare entity.

Intracranial Solitary Fibrous Tumor of the Skull Base: 2 Cases and Systematic Review of the Literature

2021 ◽  
Vol 149 ◽  
pp. e345-e359
Author(s):  
Sricharan Gopakumar ◽  
Visish M. Srinivasan ◽  
Caroline C. Hadley ◽  
Adrish Anand ◽  
Marc Daou ◽  
...  
Keyword(s):  
Systematic Review ◽  
Skull Base ◽  
Solitary Fibrous Tumor ◽  
Review Of The Literature ◽  
Fibrous Tumor

Orbital Solitary Fibrous Tumor: A Case Report and Review of the Literature

2008 ◽  
Vol 14 (2) ◽  
pp. 213-217 ◽  
Author(s):  
Giuseppe Leoncini ◽  
Vincenza Maio ◽  
Marco Puccioni ◽  
Alessandro Franchi ◽  
Vincenzo De Giorgi ◽  
...  
Keyword(s):  
Case Report ◽  
Solitary Fibrous Tumor ◽  
Review Of The Literature ◽  
Fibrous Tumor

scholarly journals Intrapulmonary Solitary Fibrous Tumor of the Lung: A Rare Case Presentation

2016 ◽  
Vol 2 (2) ◽  
pp. 42-44
Author(s):  
S Parinita ◽  
KN Mohan Rao ◽  
Vivek LNU
Keyword(s):  
Solitary Fibrous Tumor ◽  
Rare Case ◽  
Pleural Cavity ◽  
Visceral Pleura ◽  
Review Of The Literature ◽  
Case Presentation ◽  
Fibrous Tumor

ABSTRACT Localized fibrous tumors of the lung arise from the visceral pleura and are pedunculated. They also project into the pleural cavity. The tumor with an entirely pulmonary location is extremely rare. We present here a rare case of intrapulmonary localized fibrous tumor with review of the literature. How to cite this article Parinita S, Rao KNM, Vivek. Intrapulmonary Solitary Fibrous Tumor of the Lung: A Rare Case Presentation. J Med Sci 2016;2(2):42-44.

scholarly journals Solitary fibrous tumor of the hard palate: a rare entity in oral cavity

2016 ◽  
Vol 19 (1) ◽  
pp. 113
Author(s):  
Antonione Santos Bezerra Pinto ◽  
Vera Cavalcanti De Araújo ◽  
Fabrício Passador Santos ◽  
José Ferreira de Menezes Filho ◽  
Viviane Siqueira ◽  
...  
Keyword(s):  
Oral Cavity ◽  
Solitary Fibrous Tumor ◽  
Hard Palate ◽  
Salivary Gland Tumor ◽  
Immunohistochemical Analysis ◽  
Soft Tissue Tumors ◽  
Rare Entity ◽  
Gland Tumor ◽  
Clinical Imaging ◽  
Fibrous Tumor

<p align="justify"><span style="color: #000000;"><span style="font-family: Arial, serif;"><span><span lang="en-US">A case of solitary fibrous tumor is reported. Solitary fibrous tumor is a rare neoplasia characterized by the proliferation of fusiform cells of mesenchymal origin accounting for at least </span></span></span></span><span style="font-family: Arial, serif;"><span><span lang="en-US">2% of all soft tissue tumors. In this present case, the initial diagnosis was salivary gland tumor because of the location in the hard palate. </span></span></span><span style="color: #000000;"><span style="font-family: Arial, serif;"><span><span lang="en-US">Histologically, the tumor was composed by conjunctive tissue with proliferation of oval and fusiform cells. The immunohistochemical analysis was positive for CD34 and CD99. The lesion was treated by surgical resection. The clinical, imaging, histological and immunohistochemical data are discussed in this study. </span></span></span></span></p><p lang="en-US" align="justify"> </p><p align="justify"><span style="color: #000000;"><span style="font-family: Arial, serif;"><span><span lang="en-US"><strong><span>Keywords</span></strong></span></span></span></span></p><p align="justify"><span style="font-family: Arial, serif;"><span><span lang="en-US">Solitary fibrous tumor; Oral cavity; Hard palate; Differential diagnosis.</span></span></span></p><p lang="en-US" align="justify"> </p>

Solitary Fibrous Tumor of the Larynx: A Case Report and Review of the Literature

2006 ◽  
Vol 130 (2) ◽  
pp. 213-216 ◽  
Author(s):  
Jorge E. Dotto ◽  
William Ahrens ◽  
David J. Lesnik ◽  
Diane Kowalski ◽  
Clarence Sasaki ◽  
...  
Keyword(s):  
Case Report ◽  
Solitary Fibrous Tumor ◽  
Review Of The Literature ◽  
Solitary Fibrous Tumors ◽  
Subsequent Investigation ◽  
Mesenchymal Neoplasms ◽  
Fibrous Tumor

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.

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
Keyword(s):  
Case Report ◽  
Solitary Fibrous Tumor ◽  
Review Of The Literature ◽  
Floor Of The Mouth ◽  
Fibrous Tumor

scholarly journals A giant solitary fibrous tumor of the adrenal gland in a 13-year old: a case report and review of the literature

2019 ◽  
Vol 13 (1) ◽  
Author(s):  
Hailu Wondimu Gebresellassie ◽  
Yusuf Mohammed ◽  
Brahenu Kotiso ◽  
Bereket Amare ◽  
Aemero Kebede
Keyword(s):  
Case Report ◽  
Adrenal Gland ◽  
Solitary Fibrous Tumor ◽  
Review Of The Literature ◽  
Fibrous Tumor

Solitary Fibrous Tumor of the Parapharyngeal Space: A Case Report and Review of the Literature

1996 ◽  
Vol 75 (10) ◽  
pp. 681-684 ◽  
Author(s):  
Kunal Gangopadhyay ◽  
Khalid Taibah ◽  
M. Babu Manohar ◽  
Hala Kfoury
Keyword(s):  
Case Report ◽  
Head And Neck ◽  
Solitary Fibrous Tumor ◽  
Spindle Cell ◽  
Parapharyngeal Space ◽  
English Literature ◽  
Review Of The Literature ◽  
Solitary Fibrous Tumors ◽  
Rare Location ◽  
Fibrous Tumor

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.

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