Abstract
Background:
Synovial sarcoma, a rare tumor in the head and neck, has been historically diagnosed by its characteristic biphasic histologic pattern. Monophasic variants exist which can be difficult to diagnose.
Methods:
Two cases of synovial sarcoma of the head and neck are presented. Both cases, cytogenetic analysis was performed using standard protocols.
Results:
Both tumors demonstrated a chromosomal translocation, t(X;18)(p11.2;q11.2), which either made or confirmed the diagnosis.
Conclusions:
Synovial sarcoma contains a characteristic chromosomal translocation which is a useful diagnostic tool, especially when histologic studies are equivocal.
Publication types
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Case Reports
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Research Support, Non-U.S. Gov't
MeSH terms
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Adult
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Aged
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Chromosomes, Human, Pair 18 / genetics*
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Diagnosis, Differential
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Head and Neck Neoplasms / diagnosis
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Head and Neck Neoplasms / genetics*
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Head and Neck Neoplasms / pathology
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Humans
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Leiomyosarcoma / diagnosis
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Male
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Parotid Neoplasms / diagnosis
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Parotid Neoplasms / genetics
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Parotid Neoplasms / pathology
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Pharyngeal Neoplasms / diagnosis
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Pharyngeal Neoplasms / genetics
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Pharyngeal Neoplasms / pathology
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Sarcoma, Synovial / diagnosis
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Sarcoma, Synovial / genetics*
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Sarcoma, Synovial / pathology
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Skull Neoplasms / diagnosis
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Skull Neoplasms / genetics
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Skull Neoplasms / pathology
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Translocation, Genetic / genetics*
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X Chromosome / genetics*