PNET-like features of synovial sarcoma of the lung: A pitfall in the cytologic diagnosis of soft-tissue tumors

2001 ◽  
Vol 24 (4) ◽  
pp. 283-288 ◽  
Author(s):  
Pascale Hummel ◽  
Grace C.H. Yang ◽  
Ashok Kumar ◽  
Jean Marc Cohen ◽  
Barbara Winkler ◽  
...  
2018 ◽  
Vol 32 (04) ◽  
pp. 322-330 ◽  
Author(s):  
Andrea Evenski ◽  
James Stensby ◽  
Samuel Rosas ◽  
Cynthia Emory

AbstractIntra-articular (IA) and peri-articular (PA) tumors of the knee are frequently encountered by orthopaedic surgeons. Nonetheless, due to the possibility of great morbidity and potential mortality, it is important to recognize and differentiate between benign and malignant lesions in a timely manner. Therefore, the purpose of this article is to provide a concise, practical, and updated review of commonly encountered IA and PA tumors including intratendinous gout, synovial chondromatosis, schwannoma, pigmented villonodular synovitis, and synovial sarcoma, and a detailed description of differentiating features to include various imaging modalities.


1986 ◽  
Vol 2 (3) ◽  
pp. 244-247 ◽  
Author(s):  
Walter Ryd ◽  
Sanjida Mugal ◽  
Khalid Ayyash

Rare Tumors ◽  
2018 ◽  
Vol 10 ◽  
pp. 203636131877649 ◽  
Author(s):  
Kazuhiko Hashimoto ◽  
Shunji Nishimura ◽  
Kousuke Fujii ◽  
Ryosuke Kakinoki ◽  
Masao Akagi

Synovial sarcomas are malignant soft tissue tumors that carry a metastatic potential and portend poor prognoses. We report a very rare synovial sarcoma arising from the tibial nerve and describe its successful treatment including limb preservation. To the best of our knowledge, this is the 40th reported incident of intraneural synovial sarcoma, and only the fourth arising from the tibial nerve. Extensive resection of synovial sarcoma arising in the popliteal region is difficult, particularly when limb preservation is desired. Ours is the first reported patient treated for tibial nerve-derived synovial sarcoma whose limbs were preserved.


2007 ◽  
Vol 20 (5) ◽  
pp. 522-528 ◽  
Author(s):  
Rui He ◽  
Rajiv M Patel ◽  
Serhan Alkan ◽  
Rasheed Hammadeh ◽  
Sharon W Weiss ◽  
...  

2016 ◽  
Vol 106 (4) ◽  
pp. 283-288 ◽  
Author(s):  
Gary M. Lepow ◽  
Daniel L. Grimmer ◽  
Onya V. Lemar ◽  
Evan A. Bridges

The purpose of this case report is to present a rare finding of synovial sarcoma in a 5-year-old child. Most soft-tissue masses of the foot are too often presumed to be small and benign; therefore, compared with soft-tissue sarcomas, they are difficult to clinically differentiate and treat. A 5-year-old girl presented with a painful lesion that was diagnosed as synovial sarcoma after an excisional biopsy was performed. This was an unexpected finding of synovial sarcoma involving the tibialis posterior tendon of her right foot. The patient presented with an 8-month history of tenderness and an antalgic gait. We would like to encourage that all soft-tissue tumors of the foot be preoperatively evaluated with the aid of diagnostic imaging so that a well-planned biopsy assessment can be performed, with adequate margins excised.


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