2001
DOI: 10.1016/s1072-7515(00)00806-1
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Synovial Sarcoma in Children: Surgical Lessons From A Single Institution and Review of The Literature

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Cited by 75 publications
(45 citation statements)
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“…During the last several decades, much effort has been invested in determining prognostic factors affecting overall survival in patients with synovial sarcoma. Histologic subtype, tumor grade, anatomic location, age, gender, tumor size, and surgical margins have been reported to have prognostic implication for a patient's overall survival [1,2,6,9,12,16,17,[19][20][21][22][23][24]. In our study, histologic subtype, grade, anatomic location, size, age, and surgical margins did not predict overall survival.…”
Section: Discussioncontrasting
confidence: 45%
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“…During the last several decades, much effort has been invested in determining prognostic factors affecting overall survival in patients with synovial sarcoma. Histologic subtype, tumor grade, anatomic location, age, gender, tumor size, and surgical margins have been reported to have prognostic implication for a patient's overall survival [1,2,6,9,12,16,17,[19][20][21][22][23][24]. In our study, histologic subtype, grade, anatomic location, size, age, and surgical margins did not predict overall survival.…”
Section: Discussioncontrasting
confidence: 45%
“…Primary tumor size [1,2,12,16,17,[20][21][22][23]27], tumor stage [20,23], gender [6,23,27], age [2,6,12,17,19,21,27], tumor grade [6,23], histologic subtype [2,17,19,20,23], tumor necrosis [23], mitotic activity [23], invasion of bone and neurovascular structures [1,16], and anatomic tumor location [6,9,17,19,23] all influence the natural history of primary synovial sarcomas. However, many of these findings have not been consistent so definitive conclusions based on them cannot be made.…”
Section: Introductionmentioning
confidence: 99%
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“…Desmin often is positive in rhabdomyosarcoma [37,38] and it also is seen in AFH [20]. Synovial sarcoma is the most common nonrhabdomyosarcoma soft tissue malignancy seen in children, comprising 7% to 8% of all pediatric malignant soft tissue tumors [1]. Similar to AFHs, synovial sarcomas primarily occur in the extremities [22,42] and are deepseated [22].…”
Section: Discussion and Treatmentmentioning
confidence: 99%
“…Joint cavity involvement has been reported to occur in less than 5% of patients. [4,5] In the extremities, the single most common site for synovial sarcoma is the knee joint, followed by the ankle/foot, elbow, and upper arm/shoulder joint. Joint cavity involvement is rare, and the joint most commonly affected is the knee.…”
Section: Discussionmentioning
confidence: 99%