Results 141 to 150 of about 16,784 (197)
BRAF <sup><b>V600E</b></sup> Metastatic Synovial Sarcoma Treated with BRAF & MEK Inhibitors Achieves Complete Response. A Case Report & Literature Review. [PDF]
Burg D +20 more
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Tumefaction of the Parotid Region in a 10-Month-Old Infant Revealing a Synovial Sarcoma: A Diagnostic Challenge, Case Report, and Review of the Literature. [PDF]
Rachidi H +3 more
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The Journal of Dermatologic Surgery and Oncology, 1982
The authors, after a review of the world's literature and histogenetic theories, present a case of synovial sarcoma and emphasize the importance to dermatologists of knowledge of this neoplasm.
CHIMENTI S +2 more
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The authors, after a review of the world's literature and histogenetic theories, present a case of synovial sarcoma and emphasize the importance to dermatologists of knowledge of this neoplasm.
CHIMENTI S +2 more
openaire +3 more sources
Journal of Hand Surgery, 1986
The presence of a calcified mass in the soft tissue may be the result of any number of processes. Post-traumatic changes and metabolic alterations may both lead to such calcification. The presence of calcification is much less commonly seen in malignant neoplasms. A case of calcifying synovial sarcoma with unusual features was recently seen.
D S, Louis +3 more
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The presence of a calcified mass in the soft tissue may be the result of any number of processes. Post-traumatic changes and metabolic alterations may both lead to such calcification. The presence of calcification is much less commonly seen in malignant neoplasms. A case of calcifying synovial sarcoma with unusual features was recently seen.
D S, Louis +3 more
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Synovial Sarcoma of the Finger
Hand, 1982Synovial sarcoma is a rare tumour in the hand. We report an unusual case of such a tumour that was located in the distal phalanx of a finger of an elderly woman. A synovial tumour in this location and at such an age seems to be unique.
D R, Goodwin, R, Salama
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Current Diagnostic Pathology, 1994
Synovial sarcoma is a rare soft tissue tumor of children and adults that is unrelated to synovium and can occur in almost any part of the body. The familiar biphasic synovial sarcoma has discernible glandular or solid epithelial structures, and monophasic forms have characteristic ovoid or spindle cells with only immunohistochemical or ultrastructural ...
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Synovial sarcoma is a rare soft tissue tumor of children and adults that is unrelated to synovium and can occur in almost any part of the body. The familiar biphasic synovial sarcoma has discernible glandular or solid epithelial structures, and monophasic forms have characteristic ovoid or spindle cells with only immunohistochemical or ultrastructural ...
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Annals of Diagnostic Pathology, 2001
A case of synovial sarcoma of the paraspinal region showing massive cystic changes is described. The tumor presented in a 53-year-old white woman who noticed a lump on the upper aspect of her back. Magnetic resonance imaging of the cervical spine showed a heterogeneous paraspinal mass with well-defined margins and a multilocular quality with foci of ...
C, Morrison +4 more
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A case of synovial sarcoma of the paraspinal region showing massive cystic changes is described. The tumor presented in a 53-year-old white woman who noticed a lump on the upper aspect of her back. Magnetic resonance imaging of the cervical spine showed a heterogeneous paraspinal mass with well-defined margins and a multilocular quality with foci of ...
C, Morrison +4 more
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Synovial Sarcoma of the Hypopharynx
Annals of Otology, Rhinology & Laryngology, 1978— Primary synovial sarcoma of the hypopharynx is an extremely rare neoplasm. Only 16 cases could be traced in the literature so far. An additional case, in a 29-year-old male patient, is presented. Progressive disturbance of deglutition and speech, choking sensation, and mild respiratory distress were his original complaints.
B, Gapany-Gapanavicius +2 more
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Intraarticular Synovial Sarcoma
The American Journal of Surgical Pathology, 1992A 43-year-old man presented with decreased range of motion in his left knee and a painful medial joint mass that was grossly visible. Arthroscopy demonstrated a mobile, flat mass 3 cm in diameter in the knee joint that seemed to be loosely tethered to the synovium. The mass was excised, and light microscopic examination demonstrated a biphasic synovial
C D, McKinney, S E, Mills, R E, Fechner
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Synovial Sarcoma of the Tongue
Archives of Otolaryngology - Head and Neck Surgery, 1971A previously unreported primary synovial sarcoma of the tongue occurred in a 21-year-old man. Because of refusal of surgery, the lesion was treated with a radiation dose of 6,000 rads with apparent success over a two-year follow-up, an experience not in keeping with the generally known behavior of such tumors.
G M, Novotny, T C, Fort
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