scholarly journals Soft Tissue Tumors: t(X;20)(p11.23;q13.33) in Biphasic Synovial Sarcoma

2008 ◽  
Author(s):  
Clelia T. Storlazzi ◽  
Fredrik Mertens
Keyword(s):  
Soft Tissue ◽  
Synovial Sarcoma ◽  
Soft Tissue Tumors

scholarly journals Diagnostic Imaging and Management of Common Intra-articular and Peri-articular Soft Tissue Tumors and Tumorlike Conditions of the Knee

2018 ◽  
Vol 32 (04) ◽  
pp. 322-330 ◽  
Author(s):  
Andrea Evenski ◽  
James Stensby ◽  
Samuel Rosas ◽  
Cynthia Emory
Keyword(s):  
Soft Tissue ◽  
Diagnostic Imaging ◽  
Synovial Sarcoma ◽  
Synovial Chondromatosis ◽  
Soft Tissue Tumors ◽  
Pigmented Villonodular Synovitis ◽  
Villonodular Synovitis ◽  
Timely Manner ◽  
Malignant Lesions ◽  
Pigmented Villonodular

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.

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 ◽  
...  
Keyword(s):  
Soft Tissue ◽  
Synovial Sarcoma ◽  
Soft Tissue Tumors ◽  
Cytologic Diagnosis

scholarly journals Intraneural synovial sarcoma of the tibial nerve

Rare Tumors ◽  
2018 ◽  
Vol 10 ◽  
pp. 203636131877649 ◽  
Author(s):  
Kazuhiko Hashimoto ◽  
Shunji Nishimura ◽  
Kousuke Fujii ◽  
Ryosuke Kakinoki ◽  
Masao Akagi
Keyword(s):  
Soft Tissue ◽  
Synovial Sarcoma ◽  
Tibial Nerve ◽  
Metastatic Potential ◽  
Soft Tissue Tumors ◽  
Extensive Resection ◽  
Malignant Soft Tissue Tumors ◽  
Limb Preservation ◽  
Synovial Sarcomas ◽  
Malignant Soft Tissue

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.

scholarly journals Immunostaining for SYT protein discriminates synovial sarcoma from other soft tissue tumors: analysis of 146 cases

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

Synovial Sarcoma in the Foot of a 5-Year-Old Child

2016 ◽  
Vol 106 (4) ◽  
pp. 283-288 ◽  
Author(s):  
Gary M. Lepow ◽  
Daniel L. Grimmer ◽  
Onya V. Lemar ◽  
Evan A. Bridges
Keyword(s):  
Soft Tissue ◽  
Synovial Sarcoma ◽  
Soft Tissue Sarcomas ◽  
Excisional Biopsy ◽  
Soft Tissue Tumors ◽  
Tibialis Posterior ◽  
Unexpected Finding ◽  
Tibialis Posterior Tendon ◽  
History Of ◽  
Soft Tissue Masses

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.

Angiography of Histopathologic Variants of Synovial Sarcoma

1986 ◽  
Vol 27 (4) ◽  
pp. 449-454 ◽  
Author(s):  
J. F. Lois ◽  
H. J. Fischer ◽  
J. M. Mirra ◽  
A. S. Gomes
Keyword(s):  
Soft Tissue ◽  
Synovial Sarcoma ◽  
Tumor Size ◽  
Soft Tissue Tumors ◽  
Vascular Pattern ◽  
Tumor Vessels ◽  
Soft Tissue Masses ◽  
Synovial Sarcomas ◽  
Histopathologic Analysis

Synovial sarcomas are rare soft tissue tumors which histopathologically can be divided into monophasic, biphasic and mixed variants. As part of a protocol for intra-arterial chemotherapy 12 patients with biopsy proven synovial sarcoma underwent angiography. The angiograms on these patients were reviewed to determine whether synovial sarcomas and their variants demonstrated a characteristic angiographic appearance. Synovial sarcomas appeared angiographically as soft tissue masses which showed a fine network of tumor vessels with an inhomogeneous capillary blush. Their degree of vascularity varied according to their histopathology. Monophasic synovial sarcomas demonstrated in general a higher degree of neovascularity than the biphasic form. This finding was also suggested by histopathologic analysis of the vessels in the tumor. Although angiography did not show a distinctive vascular pattern it may be useful to evaluate tumor size and vascularity.

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