A Rare Case of a Vaginal Solitary Fibrous Tumor, Presenting as a Cystic Mass, Showing NAB2ex4-STAT6ex2 Fusion and STAT6 Immunostaining

2019 ◽  
Vol 38 (1) ◽  
pp. 21-26 ◽  
Author(s):  
Bharat Rekhi ◽  
Prachi Bapat ◽  
Omshree Shetty
Keyword(s):  
Solitary Fibrous Tumor ◽  
Rare Case ◽  
Cystic Mass ◽  
Fibrous Tumor

A rare case of solitary fibrous tumor of the mesorectum

Chirurgia ◽  
2018 ◽  
Vol 31 (5) ◽  
Author(s):  
Kengo Hayashi ◽  
Masanori Kotake ◽  
Hiroki Tawara ◽  
Kaichiro Karo ◽  
Koichiro Sawada ◽  
...  
Keyword(s):  
Solitary Fibrous Tumor ◽  
Rare Case ◽  
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 Extrapleural Solitary Fibrous Tumor (SFT) at Dorsum Foot - A Rare Case Report

2016 ◽  
Vol 2 (5) ◽  
Author(s):  
Singh Harpal ◽  
Ramandeep Kaur ◽  
Ramandeep Kaur ◽  
Sunita Bhagat ◽  
Ramanpreet Kaur ◽  
...  
Keyword(s):  
Case Report ◽  
Solitary Fibrous Tumor ◽  
Rare Case ◽  
Rare Case Report ◽  
Fibrous Tumor ◽  
Extrapleural Solitary Fibrous Tumor

scholarly journals Solitary Fibrous Tumor of Rectus Sheath: A Rare Case Report

2017 ◽  
Vol 3 (3) ◽  
Author(s):  
Alaka Sahu ◽  
Snigdha Rani Nahak ◽  
Salil Kumar Nayak ◽  
Kailash Chandra Agrawal
Keyword(s):  
Case Report ◽  
Solitary Fibrous Tumor ◽  
Rare Case ◽  
Rectus Sheath ◽  
Rare Case Report ◽  
Fibrous Tumor

A Rare Case of Fat-Forming Variant of Solitary Fibrous Tumor Presenting as a Pleural Mass

2011 ◽  
Vol 70 (6) ◽  
pp. 511
Author(s):  
Mi-Ae Kim ◽  
Ji-Hyun Lee ◽  
Hye Cheol Jeong ◽  
Seung Won Koo ◽  
Kyung Mi Park ◽  
...  
Keyword(s):  
Solitary Fibrous Tumor ◽  
Rare Case ◽  
Fibrous Tumor

scholarly journals A Rare Case of a Recurrent Giant Solitary Fibrous Tumor of the Ciliary Body of the Orbit

2016 ◽  
Vol 15 (S2) ◽  
pp. 378-381 ◽  
Author(s):  
Arvind Krishnamurthy ◽  
Shirley Sundar Singh ◽  
Urmila Majhi ◽  
Vijayalakshmi Ramshankar ◽  
Arvind Krishnamurthy
Keyword(s):  
Solitary Fibrous Tumor ◽  
Ciliary Body ◽  
Rare Case ◽  
Fibrous Tumor

scholarly journals A rare case of metastatic solitary fibrous tumor of the pancreas manifesting as a cystic neoplasm: a case report

2019 ◽  
Vol 5 (1) ◽  
Author(s):  
Hironori Yamashita ◽  
Yasuhiro Fujino ◽  
Tadayuki Ohara ◽  
Keitaro Kakinoki ◽  
Takemi Sugimoto ◽  
...  
Keyword(s):  
Brain Tumor ◽  
Solitary Fibrous Tumor ◽  
Rare Case ◽  
Abdominal Cavity ◽  
Brain Lesion ◽  
Mesenchymal Tumor ◽  
Neuroendocrine Neoplasm ◽  
Cystic Neoplasm ◽  
History Of ◽  
Fibrous Tumor

Abstract Background Solitary fibrous tumor (SFT) is a rare mesenchymal tumor that typically arises from the pleura. Although it may appear in other organs, it rarely develops in the pancreas. We report herein a rare case of metastatic SFT of the pancreas originating from an intracranial tumor and subsequently identified as a cystic neoplasm of the pancreas. Case presentation A 58-year-old woman with a past medical history of brain tumor visited the hospital for further investigation of a cystic tumor in the pancreas tail. Abdominal imaging showed a heterogeneously enhancing mass that was initially suspected as a neuroendocrine neoplasm, solid pseudopapillary neoplasm, or mucinous cystic neoplasm of the pancreas. Distal pancreatectomy was performed without any intraoperative and postoperative complications. Pathological findings confirmed a diagnosis of malignant SFT of the pancreas with hyperproliferative potential. A histopathological review of her brain tumor revealed that the pancreatic tumor was derived from her brain lesion. The patient developed recurrent brain disease 4 years after the pancreatectomy, but no recurrence has been observed in the abdominal cavity. Conclusions SFT should be considered in the differential diagnosis of untypical hypervascular pancreatic mass, particularly in patients with a history of an intrathoracic or intracranial mesenchymal tumor. Immunohistochemical analysis is crucial in detecting this tumor entity. Hyperproliferative status indicates a malignant disease and requires careful postoperative observation.

Solitary fibrous tumor of the lesser omentum: Report of a rare case

2010 ◽  
Vol 21 (4) ◽  
pp. 464-466 ◽  
Author(s):  
Yahya EKICI ◽  
Saban UYSAL ◽  
Gulnur GUVEN ◽  
Gokhan MORAY
Keyword(s):  
Solitary Fibrous Tumor ◽  
Rare Case ◽  
Lesser Omentum ◽  
Fibrous Tumor

A rare case of solitary fibrous tumor of the nasal cavity

2003 ◽  
Vol 30 (3) ◽  
pp. 303-305 ◽  
Author(s):  
Iordanis Konstantinidis ◽  
Stefanos Triaridis ◽  
Athanasios Triaridis ◽  
Afroditi Pantzaki
Keyword(s):  
Nasal Cavity ◽  
Solitary Fibrous Tumor ◽  
Rare Case ◽  
Fibrous Tumor

scholarly journals A Rare Case of a Solitary Fibrous Tumor of the Spermatic Cord

2021 ◽  
Vol 2021 ◽  
pp. 1-3
Author(s):  
Moyosore Awobajo ◽  
Stefanie Hettwer ◽  
Sarah Hackman
Keyword(s):  
Solitary Fibrous Tumor ◽  
Spermatic Cord ◽  
Rare Case ◽  
Surgical Excision ◽  
Mesenchymal Tumors ◽  
Solitary Fibrous Tumors ◽  
Important Differential Diagnosis ◽  
History Of ◽  
Scrotal Swelling ◽  
Fibrous Tumor

Solitary fibrous tumors (SFTs) are rare mesenchymal tumors, originally identified in the pleura. Even though they have subsequently been described in several extrapleural sites, the incidence of SFTs in the spermatic cord is particularly rare. Here, we report a case of a 27-year-old male that presented with a 3-year history of left scrotal swelling. Computed tomography (CT) and ultrasound demonstrated multiple solid, hypoechoic well-circumscribed masses that were separate from the testis. Surgical excision of the mass led to pathologic diagnosis of a solitary fibrous tumor involving the spermatic cord. Solitary fibrous tumors, although rare, are an important differential diagnosis for urogenital tumors.

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