scholarly journals Giant solitary fibrous tumour breast: a case report

2021 ◽  
Vol 8 (9) ◽  
pp. 2830
Author(s):  
Sayanna S. Shengulwar ◽  
Prasad K. R. K. ◽  
Swarnalatha S. ◽  
Purendar Reddy P. ◽  
Prapul Chandra Reddy E. ◽  
...  

Although giant solitary fibrous tumor is a rare soft tissue tumor but is to be considered in the differential diagnosis of benign breast tumors like fibroadenoma and phyllodes tumor at the time of clinical evaluation.

F1000Research ◽  
2012 ◽  
Vol 1 ◽  
pp. 63
Author(s):  
Rateesh Sareen ◽  
Pandey Chandralekha ◽  
Mohit Sareen ◽  
Akanksha Dutt

Pleuropulmonary synovial sarcoma is a diagnostic challenge. Synovial sarcoma is a soft tissue tumor of joints and extremities and are rarely seen in the mediastinum. We report this tumor at a very unusual location – the mediastinum in a 40-year-old female. The histopathology picture along with the location suggested a differential diagnosis of solitary fibrous tumor or mesothelioma, but immunohistochemistry helped in reaching the diagnosis of synovial sarcoma.


2013 ◽  
Vol 2013 ◽  
pp. 1-4
Author(s):  
Brian Cervenka ◽  
Brenda Villegas ◽  
Uttam Sinha

Solitary fibrous tumor (SFT) is a rare mesenchymal neoplasm that can present essentially anywhere in the body. Presentations in the hypopharynx are extremely rare with only two previous cases reported. We report the first case of postcricoid SFT occurring in a 58-year-old male requiring a microsuspension laryngoscopy excision following an unsuccessful transoral robotic attempt. The excision was uneventful, and the patient is currently without recurrence. Current management strategies of the hypopharyngeal SFT, the unique differential diagnosis, and challenges in surgical approaches in the postcricoid region are discussed.


Author(s):  
Saeed Sohrabpour ◽  
Reza Erfanian ◽  
Ebrahim Karimi ◽  
Farrokh Heidari

A Solitary Fibrous Tumor (SFT) is a soft tissue tumor that appears exceedingly rare in the parotid gland. The literature review suggested that approximately 12%-22% of these cases behave aggressively. Besides, only 4 cases of histological malignant parotid gland SFT are reported in the English literature. We presented a 65-year-old cigarette-smoker man with a fix and tender mass over the left parotid and submandibular areas. On physical examination, the marginal branch of the facial nerve was paralyzed. The left total parotidectomy and neck dissection levels 1 and 2 were performed with preoperative embolization procedure and adjuvant radiotherapy for the patient. The results of the follow-up examination were unremarkable after 11 months. In this case report, we aimed to increase awareness on SFTs, although rare, among clinicians and pathologists. Accordingly, it should be considered in the differential diagnosis of soft-tissue tumors in the major salivary glands for better management.


2010 ◽  
Vol 43 (1) ◽  
pp. 60-64 ◽  
Author(s):  
Takashi Yuri ◽  
Sayaka Kanematsu ◽  
Yen-Chang Lei ◽  
Maki Kuwata ◽  
Masaharu Oishi ◽  
...  

1992 ◽  
Vol 6 (4) ◽  
pp. 135-137 ◽  
Author(s):  
Ari Namon

Nonepithilial tumors of the nasal cavity, paranasal sinuses, and nasopharynx are uncommon. Awareness of the variety of tumors to be found and their distinguishing characteristics allows for proper diagnosis and treatment. We present a case of solitary fibrous tumor of the sinonasal tract with a discussion of its differential diagnosis, evaluation, and treatment.


2010 ◽  
Vol 59 (4) ◽  
pp. 830-835
Author(s):  
Yoshihiro Nozaki ◽  
Masato Tomita ◽  
Rintaro Ikeda ◽  
Hideyuki Hayashi ◽  
Masataka Uetani ◽  
...  

2021 ◽  
Vol 25 ◽  
pp. 200530
Author(s):  
Amintas Samuel ◽  
Laurent Elodie ◽  
Gros Audrey ◽  
Sesboue Come ◽  
Merlio Jean-Philippe ◽  
...  

2021 ◽  
Vol 7 (1) ◽  
Author(s):  
Kozue Matsuishi ◽  
Kojiro Eto ◽  
Atsushi Morito ◽  
Hirokazu Hamasaki ◽  
Keisuke Morita ◽  
...  

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.


2021 ◽  
Author(s):  
Ali Sheikhy ◽  
Aida Fallahzadeh ◽  
Seyed Hossein Ahmadi‐Tafti ◽  
Kaveh Hosseini ◽  
Reza Mohseni‐Badalabadi ◽  
...  

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