scholarly journals Solitary Fibrous Tumor of the Paraspinal Region: A Case Report

2018 ◽  
Vol 15 (3) ◽  
pp. 59-61
Author(s):  
Rajeev Bhandari ◽  
Prakash Bista ◽  
Rajiv Jha ◽  
Rajendra Shrestha ◽  
Bikesh Khambu
Keyword(s):  
Solitary Fibrous Tumor ◽  
Case Reports ◽  
Low Back ◽  
Wide Range ◽  
Left Lower Limb ◽  
Function Test ◽  
The Central Nervous System ◽  
Spinal Region ◽  
Fibrous Tumor ◽  
Imaging Patient

Solitary fibrous tumor (SFT) is a rare neoplasm occurring in the central nervous system. It rarely occurs in the spine. SFTs represent a wide range of neoplasm's, ranging from benign to malignant. This case reports on a 51 year- old male with localized solitary fibrous tumor on left para spinal region which was observed by Magnetic Resonance Imaging. Patient complained a low back pain radiating to left lower limb for successive 10 days. Laboratory investigation such as CBC and renal function test was normal. A Confirmation of patients Solitary fibrous tumor (SFT) was done on the basis of surgical, radiological, histological and immunohisto chemical findings.

Solitary fibrous tumor of the central nervous system: a clinicopathologic study of 24 cases

2011 ◽  
Vol 154 (2) ◽  
pp. 237-248 ◽  
Author(s):  
Hong Chen ◽  
Xian-Wei Zeng ◽  
Jin-Song Wu ◽  
Ya-Fang Dou ◽  
Yin Wang ◽  
...  
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Solitary Fibrous Tumor ◽  
Clinicopathologic Study ◽  
System A ◽  
The Central Nervous System ◽  
Fibrous Tumor

scholarly journals Malignant Solitary Fibrous Tumor of the Right Cerebellum: A Case Report

2021 ◽  
Vol 13 (1) ◽  
pp. 259-266
Author(s):  
Ye-Tao Zhu ◽  
Yang Liu ◽  
Li-Gang Chen ◽  
Da-Ping Song
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Solitary Fibrous Tumor ◽  
Immunohistochemical Staining ◽  
Biological Behavior ◽  
Resonance Imaging ◽  
Solitary Fibrous Tumors ◽  
The Central Nervous System ◽  
Fibrous Tumor ◽  
The Right

Solitary fibrous tumor is a very rare mesenchymal tumor that occurs mostly in the pleura, and there are few reported cases of a presence in the central nervous system, particularly in the cerebellum. In 2016, the WHO classified solitary fibrous tumors into grade I. In this article, we present a case of malignant solitary fibrous tumor recurring 8 years after surgery in a 63-year-old male. Magnetic resonance imaging showed low to intermediate mixed signal intensity on T1W1. Immunohistochemical staining positivity for Vimentin, CD99, CD34 and Bcl-2, it is consistent with the immunohistochemical characteristics of solitary fibrous tumor. We resected the patient’s tumor, and the patient was followed up for 3 months with no signs of recurrence. Solitary fibrous tumors are very rare in the central nervous system. Immunohistochemical staining positivity for CD34 and Bcl-2 is strongly expressed in most solitary fibrous tumor. Surgical resection is the preferred treatment. Due to the small number of cases, the biological behavior and prognosis of this tumor need to be further explored.

scholarly journals Spinal location is prognostic of survival for solitary-fibrous tumor/hemangiopericytoma of the central nervous system

2019 ◽  
Vol 143 (3) ◽  
pp. 457-464 ◽  
Author(s):  
Deborah Boyett ◽  
Connor J. Kinslow ◽  
Samuel S. Bruce ◽  
Adam M. Sonabend ◽  
Ali I. Rae ◽  
...  
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Solitary Fibrous Tumor ◽  
The Central Nervous System ◽  
Fibrous Tumor

Solitary fibrous tumor: A Brazilian cohort analysis.

2019 ◽  
Vol 37 (15_suppl) ◽  
pp. 11068-11068
Author(s):  
Marcelle Goldner Cesca ◽  
Celso Lopes Mello ◽  
Tiago Felismino ◽  
Maria Nirvana Formiga ◽  
Ulisses Ribaldo Nicolau ◽  
...  
Keyword(s):  
Solitary Fibrous Tumor ◽  
Systemic Treatment ◽  
Cohort Analysis ◽  
Locally Advanced ◽  
Soft Tissue Sarcomas ◽  
Primary Objective ◽  
The Body ◽  
Cancer Center ◽  
Wide Range ◽  
Fibrous Tumor

11068 Background: Solitary fibrous tumor (SFT) is a rare mesenchymal tumor that account for less than 2% of all soft tissue sarcomas. SFT has been identified in multiple anatomic locations and can arise anywhere in the body. Surgical management is the mainstay of treatment for localized disease. However, about 20% will develop locoregional recurrences or distant metastasis with a role for systemic treatment. Methods: A retrospective analysis was carried out in a large cancer center in Brazil. Our primary objective was to evaluate clinical and treatment aspects of metastatic/ locally advanced (Mtx/LA) SFT cohort and secondary to describe clinical characteristics of entire population diagnosed with SFT. Descriptive statistics was used for main results. Survival curves were estimated using Kaplan-Meier. Data were retrieved from electronic patient medical records. Results: From April, 1971 to October, 2017, 82 patients with SFT were treated. Median follow-up was 45.5 months. 67 (81.7%) were alive on the cut-off date. Median age at diagnosis was 51 (14-78). 40.2% men. Most common primary sites (PS) were pleura (19.8%), central nervous system (CNS - 11%) and pelvis (11%). 18 (21.9%) underwent chemotherapy for Mtx/LA disease. In this subgroup, 61.1% were men; PS retroperitoneal (22.2%), extremities (16.7%), CNS (16.7%). 66.7% had pulmonary, 44.4% hepatic, 27.8% bone metastasis and one (5.5%) local recurrence. All patients had at least one adverse prognostic factor (tumor size ≥ 10cm, positive margins, necrosis, ≥ 4/10 mitosis). One (5,5%) had Doege-Potter syndrome. 7 (38.9%) did one, 5 (27.8%) two and 6 (33.3%) ≥ 3 lines of treatment. First line was temozolomide/bevacizumab (TMZ/Bev) in 55.6%, followed by chemotherapy (Ch) in 27.8% and tyrosine kinase inhibitors (TKI) in 16.7%. Median progression-free survival was 3.5 months (95% IC: 0.0-7.4) and overall survival 27.3 months (95% IC: 18.7-36.0). Response rate using RECIST criteria was 12.5% for TMZ/Bev and 62.5% had stable disease. TKI and Ch had no response. Conclusions: SFT is rare and with heterogeneous clinical presentation. In our analysis, patients received a wide range of therapy, reflecting the lack of well-established systemic treatment option. TMZ/Bev showed consistent activity in Mtx/LA scenario.

scholarly journals Solitary fibrous tumor of the pleura: 3 case reports

2015 ◽  
Vol 61 (3) ◽  
pp. 207-208 ◽  
Author(s):  
Elias Amorim
Keyword(s):  
Solitary Fibrous Tumor ◽  
Case Reports ◽  
Benign Lesion ◽  
Complete Resection ◽  
The Other ◽  
Posterolateral Thoracotomy ◽  
Pertinent Literature ◽  
Complete Surgical Resection ◽  
Fibrous Tumor

Summary Introduction: solitary fibrous tumor of the pleura (SFTP) is a rare tumor arising from mesenchymatous cells in submesothelial pleural tissue which, unlike mesothelioma, is not related to asbestos or smoking. Methods: report of four patients who underwent surgical treatment for giant SFTP and review of the pertinent literature. Results: of the four patients operated, two presented symptoms including cough, chest pain and feeling of compression, whereas the other two subjects were asymptomatic. All patients underwent complete surgical resection by wide posterolateral thoracotomy, and surgical specimens removed with minimum bleeding. None of the cases required complementary lobectomy or segmentectomy. All tumors were histologically benign. Conclusion: complete resection of the lesion is the treatment of choice in all SFTP cases. Prognosis of the benign lesion is excellent, although close follow-up is necessary. In the rarer, more aggressive forms, treatment may be complemented by adjunctive chemotherapy or radiotherapy, the benefits of which have yet to be confirmed.

scholarly journals Two case reports of rare diseases occurring in rare parts: splenic vein solitary fibrous tumor and liver solitary fibrous tumor

2021 ◽  
Vol 5 ◽  
pp. 17-17
Author(s):  
Wenjing Wang ◽  
Banghe Bao ◽  
Anbin Hu ◽  
Xiaofeng Zhu ◽  
Qing Chen
Keyword(s):  
Rare Diseases ◽  
Solitary Fibrous Tumor ◽  
Case Reports ◽  
Splenic Vein ◽  
Fibrous Tumor

A case of solitary fibrous tumor/hemangiopericytoma in the central nervous system with papillary morphology

2019 ◽  
Vol 39 (2) ◽  
pp. 141-146
Author(s):  
Lijuan Cao ◽  
Xialing Zhang ◽  
Yin Wang ◽  
Yun Bao ◽  
Feng Tang
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Solitary Fibrous Tumor ◽  
The Central Nervous System ◽  
Fibrous Tumor

Solitary fibrous tumor of pleura and lung: case reports and literature review

2016 ◽  
pp. 33 ◽  
Author(s):  
A. A. Pechetov ◽  
Iu. S. Esakov ◽  
A. Iu. Gritsiuta ◽  
D. V. Kalinin ◽  
N. K. Ratnikova ◽  
...  
Keyword(s):  
Literature Review ◽  
Solitary Fibrous Tumor ◽  
Case Reports ◽  
Fibrous Tumor

scholarly journals Solitary Fibrous Tumor of the Lumbar Spine: The Great Mimicker—Report of the Fifth Case

2014 ◽  
Vol 2014 ◽  
pp. 1-3
Author(s):  
Amer Sebaaly ◽  
Lara Raffoul ◽  
Ronald Moussa
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Differential Diagnosis ◽  
Surgical Treatment ◽  
Lumbar Spine ◽  
Solitary Fibrous Tumor ◽  
Rare Neoplasm ◽  
The Central Nervous System ◽  
Fibrous Tumor

Solitary fibrous tumor (SFT) is a rare neoplasm occurring in the central nervous system. It rarely occurs in the spine. This paper reports the fifth case of SFT in a 34-year-old female and focusses on differential diagnosis and importance of surgical treatment.

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