scholarly journals Retroperitoneal fibrous tumor recurring as lung metastases after 10 years: a case report

2021 ◽  
Vol 7 (1) ◽  
Author(s):  
Kozue Matsuishi ◽  
Kojiro Eto ◽  
Atsushi Morito ◽  
Hirokazu Hamasaki ◽  
Keisuke Morita ◽  
...  
Keyword(s):  
Case Report ◽  
Solitary Fibrous Tumor ◽  
Distant Metastasis ◽  
Curative Resection ◽  
Lung Metastases ◽  
Lung Resection ◽  
Left Lung ◽  
Metastatic Lesion ◽  
Case Presentation ◽  
Fibrous Tumor

Abstract Background Solitary fibrous tumor (SFT) is a relatively rare mesenchymal tumor that mainly affects adults. Its prognosis is good after curative resection, but distant recurrences after 10 years or longer have been reported. Recurrent SFT usually arises as a local lesion; distant metastasis is rarely reported. Here, we report lung metastases that recurred a decade after excising a retroperitoneal primary SFT. Case presentation A 44-year-old woman had an SFT resected from her right retroperitoneum at our hospital. Ten years later, at age 54, she underwent a lung resection after CT showed three suspected metastases in her left lung. All three were histologically diagnosed as lung metastases from the retroperitoneal SFT. However, whereas the primary SFT had 1–2 mitotic cells/10 high power fields (HPF), the metastatic lesion increased malignancy, at 50/10 HPF. Conclusion Patients who have had resected SFTs should be carefully followed up, as malignancy may change in distant metastasis, as in this case.

scholarly journals Salvage carbon ion radiotherapy for recurrent solitary fibrous tumor: A case report and literature review

2020 ◽  
Vol 28 (1) ◽  
pp. 230949901989609
Author(s):  
Kazuma Murata ◽  
Kenji Endo ◽  
Takato Aihara ◽  
Yuji Matsuoka ◽  
Hirosuke Nishimura ◽  
...  
Keyword(s):  
Spinal Cord ◽  
Case Report ◽  
Solitary Fibrous Tumor ◽  
Clinical Course ◽  
Metastatic Lesion ◽  
Carbon Ion Radiotherapy ◽  
Thoracic Spinal Cord ◽  
Carbon Ion ◽  
Thoracic Spinal ◽  
Fibrous Tumor

Background: Malignant solitary fibrous tumor (MSFT) arising from the spinal cord is extremely rare and poorly understood mesenchymal neoplasms: only a few MSFT in the spinal canal has been described. We describe the clinical course of the patient with MSFT arising from the thoracic spinal cord. Case report: We describe the clinical course of the patient and the radiological and pathological findings of the tumor. The tumor had been resected by microscopic posterior approach and video-assisted thoracic surgery, but local recurrence was observed by MRI at 1-year follow-up period. No metastatic lesion was confirmed. Then, carbon ion radiotherapy (CIRT) was administered to the recurrent lesion. Local suppression has been observed for 40 months after irradiation. Conclusion: Dumbbell-shaped MSFT arising from thoracic spinal cord is a highly unusual presentation. CIRT might be effective for treatment of recurrent tumors.

scholarly journals Solitary Fibrous Tumor/Hemangiopericytoma of the Cervical Spine – A Case Report

2021 ◽  
Author(s):  
haggai suisa ◽  
Galia Ronen ◽  
Ayelet Eran ◽  
Gil Ephraim Sviri ◽  
Euvgeni Vlodavsky
Keyword(s):  
Case Report ◽  
Cervical Spine ◽  
Solitary Fibrous Tumor ◽  
Neurophysiological Monitoring ◽  
En Bloc ◽  
Ki 67 ◽  
Case Presentation ◽  
Progressive Loss ◽  
Contrast Enhanced ◽  
Fibrous Tumor

Abstract Introduction: Due to its rarity, the clinical and radiological characteristics of spinal solitary fibrous tumors/hemangiopericytomas remain largely unknown, with only 68 cases documented worldwide between 2000 and 2017. Case Presentation: We report a case of a 39-year-old female patient who presented to the emergency department with complaints of persisting headaches, a numbing sensation in both arms and a progressive loss of manual dexterity. Physical and neurological examinations were unremarkable. A cervical contrast-enhanced MRI revealed an intradural intramedullary space-occupying lesion at the C3 level, accompanied by extensive edema. The patient underwent a successful cervical laminoplasty under neurophysiological monitoring with en-bloc removal of the mass. She experienced total resolution of her symptoms. Biopsy revealed a grade I solitary fibrous tumor/hemangiopericytoma of the cervical spine, positive for CD34 and STAT6. Ki-67 index was 2%. Conclusion: This case report combines a rare tumor subtype with a unique presentation, and may further advance our understanding of this clinical entity.

scholarly journals Intravascular large B-cell lymphoma involving pleural solitary fibrous tumor: A case report and literature review

2021 ◽  
Vol 25 ◽  
pp. 200530
Author(s):  
Amintas Samuel ◽  
Laurent Elodie ◽  
Gros Audrey ◽  
Sesboue Come ◽  
Merlio Jean-Philippe ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
B Cell ◽  
Solitary Fibrous Tumor ◽  
Cell Lymphoma ◽  
B Cell Lymphoma ◽  
Large B Cell Lymphoma ◽  
Fibrous Tumor ◽  
Large B Cell

scholarly journals Solitary fibrous tumor of the greater omentum: case report and review of literature

2021 ◽  
Vol 7 (1) ◽  
Author(s):  
Karim M. Eltawil ◽  
Carly Whalen ◽  
Bryce Knapp
Keyword(s):  
Solitary Fibrous Tumor ◽  
Management Strategy ◽  
Abdominal Mass ◽  
Lower Abdominal Pain ◽  
Greater Omentum ◽  
Team Approach ◽  
Review Of Literature ◽  
Case Presentation ◽  
Multidisciplinary Team Approach ◽  
Fibrous Tumor

Abstract Background Solitary fibrous tumor (SFT) is a rare neoplasm of mesenchymal origin occurring most often in the visceral pleura, however, it has been described in almost every anatomic location of the human body. While most SFTs have a benign behavior, they can potentially be locally aggressive and demonstrate a malignant behavior. Case presentation A 63 year-old male patient presented with lower abdominal pain and nausea and was noted on CT to have a large, heterogeneous lower abdominal mass with no evidence of metastatic disease. A surgical resection was performed and the mass appeared to be connected to the greater omentum with a vascular pedicle. It was not invading any intra-abdominal or pelvic organs. Pathology revealed an SFT of omental origin. The mitotic count was less than 4 per 10 high-power fields and all pathologic characteristics did not meet the criteria for a malignant SFT. Conclusions We report an extremely rare case of SFT originating from the greater omentum. A multidisciplinary team approach was followed to plan the patient’s management strategy.

Intrapericardial solitary fibrous tumor: A case report and review of literature

2021 ◽  
Author(s):  
Ali Sheikhy ◽  
Aida Fallahzadeh ◽  
Seyed Hossein Ahmadi‐Tafti ◽  
Kaveh Hosseini ◽  
Reza Mohseni‐Badalabadi ◽  
...  
Keyword(s):  
Case Report ◽  
Solitary Fibrous Tumor ◽  
Review Of Literature ◽  
Fibrous Tumor

Solitary Fibrous Tumor of the Sella Mimicking Pituitary Adenoma: An Uncommon Tumor in a Rare Location—A Case Report

2009 ◽  
Vol 20 (1) ◽  
pp. 56-61 ◽  
Author(s):  
Tania Weber Furlanetto ◽  
Cláudio Faria Pitta Pinheiro ◽  
Paulo Petry Oppitz ◽  
Luiz Carlos de Alencastro ◽  
Sylvia L. Asa
Keyword(s):  
Case Report ◽  
Pituitary Adenoma ◽  
Solitary Fibrous Tumor ◽  
Rare Location ◽  
Fibrous Tumor ◽  
Uncommon Tumor

scholarly journals Solitary fibrous tumor of pleura: a case report and review of clinical, radiographic and histologic findings

2009 ◽  
Vol 3 (5) ◽  
Author(s):  
Vishal Kumar Agarwal ◽  
Benjamin Eric Plotkin ◽  
Donny Dumani ◽  
Samuel W. French ◽  
Ronald Becker ◽  
...  
Keyword(s):  
Case Report ◽  
Solitary Fibrous Tumor ◽  
Fibrous Tumor

scholarly journals Solitary Fibrous Tumor of the Nasopharynx. A Case Report.

1993 ◽  
Vol 86 (10) ◽  
pp. 1419-1423
Author(s):  
Yuki Minami ◽  
Yoshihiro Tsuruta ◽  
Katsuari Yane ◽  
Osamu Tanaka ◽  
Hiroshi Miyahara ◽  
...  
Keyword(s):  
Case Report ◽  
Solitary Fibrous Tumor ◽  
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.

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