Results 181 to 190 of about 29,165 (230)
Some of the next articles are maybe not open access.
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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Asian Cardiovascular and Thoracic Annals, 2013
We describe the case of a 36-year-old man who presented with chest pain and a mass lesion occupying 2/3rds of the left hemithorax on a chest radiograph. A malignant pulmonary tumor was suspected, and after all diagnostic procedures, spindle-cell carcinoma was considered.
Koray, Aydogdu +3 more
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We describe the case of a 36-year-old man who presented with chest pain and a mass lesion occupying 2/3rds of the left hemithorax on a chest radiograph. A malignant pulmonary tumor was suspected, and after all diagnostic procedures, spindle-cell carcinoma was considered.
Koray, Aydogdu +3 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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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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Skeletal Radiology, 1997
This report describes and discusses the clinical, MRI, and pathologic findings in a case of synovial sarcoma arising within a peripheral nerve. Intraneural origin of synovial sarcoma is very unusual, and the MR imaging appearance of this condition has not been previously reported.
A, Spielmann +3 more
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This report describes and discusses the clinical, MRI, and pathologic findings in a case of synovial sarcoma arising within a peripheral nerve. Intraneural origin of synovial sarcoma is very unusual, and the MR imaging appearance of this condition has not been previously reported.
A, Spielmann +3 more
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Otolaryngology–Head and Neck Surgery, 1980
Synovial sarcoma of the head and neck is a rare lesion. Based on previous literature reports, these lesions carry a poor prognosis. Case reports of two patients diagnosed and treated recently for head and neck lesions of this type are presented. A review of pathologic sections at the Armed Forces Institute of Pathology (AFIP) suggests that this lesion ...
R H, Hirokawa +2 more
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Synovial sarcoma of the head and neck is a rare lesion. Based on previous literature reports, these lesions carry a poor prognosis. Case reports of two patients diagnosed and treated recently for head and neck lesions of this type are presented. A review of pathologic sections at the Armed Forces Institute of Pathology (AFIP) suggests that this lesion ...
R H, Hirokawa +2 more
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RETINAL Cases & Brief Reports, 2017
Purpose: To describe the first reported case of intraocular synovial sarcoma. Methods: A 29-year-old man was enucleated for a blind, painful eye. Pathologic examination revealed an unexpected intraocular spindle cell tumor.
Nikisha Q, Richards +3 more
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Purpose: To describe the first reported case of intraocular synovial sarcoma. Methods: A 29-year-old man was enucleated for a blind, painful eye. Pathologic examination revealed an unexpected intraocular spindle cell tumor.
Nikisha Q, Richards +3 more
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Intravascular synovial sarcoma
Human Pathology, 1987A biphasic synovial sarcoma occurring in the wall of a pathologically thickened femoral vein was diagnosed in a 34-year-old woman. This sarcoma was resected together with removal of a thrombus. A local recurrence was seen 5 years later, but the patient is alive and well 11 years after the first operation.
M, Miettinen, S, Santavirta, P, Slätis
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Ophthalmology, 2006
To describe the clinicopathologic and immunohistochemical features and treatment of a rare case of primary synovial sarcoma of the orbit.Retrospective interventional case report.A 14-year-old young man with histologically proven synovial sarcoma of the orbit.
Morris E, Hartstein +3 more
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To describe the clinicopathologic and immunohistochemical features and treatment of a rare case of primary synovial sarcoma of the orbit.Retrospective interventional case report.A 14-year-old young man with histologically proven synovial sarcoma of the orbit.
Morris E, Hartstein +3 more
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Journal of Cardiac Surgery, 2009
Synovial sarcomas of the pericardium are very rare. This report describes the case of a 61-year-old man presenting with increasing dyspnea on exertion and recurrent pericardial effusions. Echocardiography, computed tomography, and magnetic resonance imaging demonstrated a 6 x 4-cm pericardial mass lying predominantly over the left atrium.
Narain, Moorjani +3 more
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Synovial sarcomas of the pericardium are very rare. This report describes the case of a 61-year-old man presenting with increasing dyspnea on exertion and recurrent pericardial effusions. Echocardiography, computed tomography, and magnetic resonance imaging demonstrated a 6 x 4-cm pericardial mass lying predominantly over the left atrium.
Narain, Moorjani +3 more
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