Results 151 to 160 of about 17,376 (193)
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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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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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International Journal of Pediatric Otorhinolaryngology, 1993
Synovial sarcomas are very uncommon and highly malignant tumours. This uncommon malignant tumour of mesenchymal origin may rarely present in the neck. Since 1954, nearly 80 cases of synovial sarcoma, located in the head and neck region have been reported. Synovial sarcoma is most prevalent in adolescents and young adults between 15 and 40 years of age.
M, Onerci +4 more
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Synovial sarcomas are very uncommon and highly malignant tumours. This uncommon malignant tumour of mesenchymal origin may rarely present in the neck. Since 1954, nearly 80 cases of synovial sarcoma, located in the head and neck region have been reported. Synovial sarcoma is most prevalent in adolescents and young adults between 15 and 40 years of age.
M, Onerci +4 more
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Heart, Lung and Circulation, 2006
We report a case of synovial sarcoma of the heart in a 14-year-old boy, who presented with signs of mild generalized illness and rapidly progressed to haemodynamic collapse. On operation the tumour was attached to the tricuspid valve, away from the atrioventricular node.
Sylvio Carvalho, Provenzano +3 more
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We report a case of synovial sarcoma of the heart in a 14-year-old boy, who presented with signs of mild generalized illness and rapidly progressed to haemodynamic collapse. On operation the tumour was attached to the tricuspid valve, away from the atrioventricular node.
Sylvio Carvalho, Provenzano +3 more
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ORL, 2004
<i>Background:</i> Synovial sarcoma is a soft tissue sarcoma rarely seen in the head and neck. Due to its rarity and morphologic variations, diagnosis is difficult in most cases. <i>Method:</i> A case of synovial sarcoma arising in the upper neck is presented. The detection of the specific chromosomal translocation t(X;18)(p11.2;
Naoki, Ochi +6 more
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<i>Background:</i> Synovial sarcoma is a soft tissue sarcoma rarely seen in the head and neck. Due to its rarity and morphologic variations, diagnosis is difficult in most cases. <i>Method:</i> A case of synovial sarcoma arising in the upper neck is presented. The detection of the specific chromosomal translocation t(X;18)(p11.2;
Naoki, Ochi +6 more
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European Archives of Oto-Rhino-Laryngology, 1997
Primary synovial sarcoma of the head and neck region is a rare tumor. This report describes seven cases of primary synovial sarcomas, of which two were in the parapharyngeal region, two in the supraclavicular region, and one each in the hypopharynx, sternocleidomastoid and submandibular regions.
D C, Doval +5 more
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Primary synovial sarcoma of the head and neck region is a rare tumor. This report describes seven cases of primary synovial sarcomas, of which two were in the parapharyngeal region, two in the supraclavicular region, and one each in the hypopharynx, sternocleidomastoid and submandibular regions.
D C, Doval +5 more
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The Journal of Foot and Ankle Surgery, 2013
We report the case of a 75-year-old male who underwent lung lobectomy for presumed lung cancer. Thereafter, he presented with a painful mass between the third and fourth metatarsal heads in the foot that was assumed to be Morton's neuroma. After extensive oncologic evaluation, the foot mass was diagnosed as a synovial sarcoma.
Mikhail, Bekarev +4 more
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We report the case of a 75-year-old male who underwent lung lobectomy for presumed lung cancer. Thereafter, he presented with a painful mass between the third and fourth metatarsal heads in the foot that was assumed to be Morton's neuroma. After extensive oncologic evaluation, the foot mass was diagnosed as a synovial sarcoma.
Mikhail, Bekarev +4 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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Synovial sarcoma of the kidney
Annals of Diagnostic Pathology, 2008The renal parenchyma is a rare site of origin for primary synovial sarcoma (SS). The present study describes the clinicopathologic, immunohistochemical, and molecular analysis of 7 cases of SS occurring in the kidney. There were 5 female and 2 male patients, with an age range of 15 to 46 years.
Mukul, Divetia +3 more
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Synovial sarcoma of the extremities
International Orthopaedics, 1993From May 1985 to March 1990, 18 cases of Enneking's stage II synovial sarcoma of the extremities were treated by a combination of surgery and CYVADIC chemotherapy with or without radiotherapy. The average follow up was 34.7 months. The estimated 5-year survival rate was 78.4% and the continuously disease-free 5-year survival rate was 44.4%. The results
S Y, Lee, D G, Jeon, S S, Kim
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