1994
DOI: 10.1002/mpo.2950230112
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Synovial sarcoma of the larynx in a child: Case report and histological appearances

Abstract: Synovial sarcoma of the larynx is extremely rare having been reported only six times previously in the literature. We add another case report, which to our knowledge is the first recorded case in a child. We discuss the alternative approach of combination chemotherapy and radiotherapy which in this case led to a remission lasting about 3 years. The immunohistological and ultrastructural characteristics of the tumour are also presented.

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Cited by 23 publications
(14 citation statements)
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“…Only two cases underwent chemotherapy to whom ifosfamide was given in high doses. 3,12 In our case a chemotherapy consisting of ifosfamide and adriamycin were applied. The therapy was effective and the metastatic nodules disappeared.…”
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confidence: 89%
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“…Only two cases underwent chemotherapy to whom ifosfamide was given in high doses. 3,12 In our case a chemotherapy consisting of ifosfamide and adriamycin were applied. The therapy was effective and the metastatic nodules disappeared.…”
mentioning
confidence: 89%
“…The literature includes about 10 cases of synovial sarcoma of the larynx. [2][3][4]6,7,[9][10][11][12][13][14] Most cases were treated either with surgery alone or combined with radiotherapy. Only two cases were reported to whom chemotherapy was administered.…”
Section: Introductionmentioning
confidence: 99%
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“…However, it may also arise in unexpected sites, such as head and neck regions1 and even the genitourinary tract 2. Primary intra-abdominal or retroperitoneal synovial sarcoma is a rare condition.…”
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confidence: 99%
“…In most cases it arises from the pharyngeal region rather than from other structures [5,[9][10][11][12][13][14][15][16][17][18][19].…”
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confidence: 99%