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Erratum: Malignant Peripheral Nerve Sheath Tumors with t(X;18). A Pathologic and Molecular Genetic Study
Spindle cell sarcomas often present the surgical pathologist with a considerable diagnostic challenge. Malignant peripheral nerve sheath tumor, leiomyosarcoma, fibrosarcoma, and monophasic synovial sarcoma may all appear similar histologically. The application of ancillary diagnostic modalities, suc...
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Published in: | Modern pathology 2000-12, Vol.13 (12), p.1336-1346 |
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description | Spindle cell sarcomas often present the surgical pathologist with a considerable diagnostic challenge. Malignant peripheral nerve sheath tumor, leiomyosarcoma, fibrosarcoma, and monophasic synovial sarcoma may all appear similar histologically. The application of ancillary diagnostic modalities, such as immunohistochemistry and electron microscopy, may be helpful in the differentiation of these tumors, but in cases in which these adjunctive techniques fail to demonstrate any more definitive evidence of differentiation, tumor categorization may remain difficult. Cytogenetic and molecular genetic characterization of tumors have provided the basis for the application of molecular assays as the newest components of the diagnostic armamentarium. Because the chromosomal translocation t(X;18) has been observed repeatedly in many synovial sarcomas, it has been heralded as a diagnostic hallmark of synovial sarcoma. To formally test the specificity of this translocation for the diagnosis of synovial sarcoma, RNA extracted from formalin-fixed, paraffin-embedded tissue from a variety of soft tissue and spindle cell tumors was evaluated for the presence of t(X;18) by reverse transcriptase-polymerase chain reaction. Although 85% of the synovial sarcomas studied demonstrated t(X;18), 75% of the malignant peripheral nerve sheath tumors in our cohort also demonstrated this translocation. We conclude that the translocation t(X;18) is not specific to synovial sarcoma and discuss the implications of the demonstration of t(X;18) in a majority of malignant peripheral nerve sheath tumors. |
doi_str_mv | 10.1038/modpathol.3880247 |
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We conclude that the translocation t(X;18) is not specific to synovial sarcoma and discuss the implications of the demonstration of t(X;18) in a majority of malignant peripheral nerve sheath tumors.</description><subject>Chromosomal translocation</subject><subject>Erratum</subject><subject>Laboratory Medicine</subject><subject>malignant peripheral nerve sheath tumor</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Pathology</subject><subject>specificity</subject><subject>synovial sarcoma</subject><subject>t(X;18)</subject><issn>0893-3952</issn><issn>1530-0285</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><recordid>eNp9kE9PwkAQxTdGExH9AN72qIfi_qHtVk6EIJqAkoCJt2bbndIlbZfsthi-vasQj5xmMpnfmzcPoXtKBpRw8VQbtZNtaaoBF4KwYXyBejTkJCBMhJeoR0TCA56E7BrdOLclhA5DwXqonFor265-xgtZ6U0jmxYvwepdCVZW-B3sHvCqBK-N111trMPf2vftw9eIiscBHuPl312z0TmWjcILU0HeVdLiGTTQ-umq7dThFl0VsnJwd6p99PkyXU9eg_nH7G0yngc5YyIO4ogIykjB4pgJmnHJYcgLJrKCkjCHJONA4zjkQAhhNIuySCVRopQKIyHCJOF9RI-6uTXOWSjSndW1tIeUkvQ3qvQ_qvQUlWfYkXF-t9mATbems423eRYaHSHw3-y1h1yuoclBaQt5myqjz9A_Zw-DrA</recordid><startdate>20001201</startdate><enddate>20001201</enddate><creator>O'Sullivan, Maureen J</creator><creator>Kyriakos, Michael</creator><creator>Zhu, Xiaopei</creator><creator>Wick, Mark R</creator><creator>Swanson, Paul E</creator><creator>Dehner, Louis P</creator><creator>Humphrey, Peter A</creator><creator>Pfeifer, John D</creator><general>Elsevier Inc</general><general>Nature Publishing Group US</general><scope>6I.</scope><scope>AAFTH</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20001201</creationdate><title>Erratum: Malignant Peripheral Nerve Sheath Tumors with t(X;18). 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Cytogenetic and molecular genetic characterization of tumors have provided the basis for the application of molecular assays as the newest components of the diagnostic armamentarium. Because the chromosomal translocation t(X;18) has been observed repeatedly in many synovial sarcomas, it has been heralded as a diagnostic hallmark of synovial sarcoma. To formally test the specificity of this translocation for the diagnosis of synovial sarcoma, RNA extracted from formalin-fixed, paraffin-embedded tissue from a variety of soft tissue and spindle cell tumors was evaluated for the presence of t(X;18) by reverse transcriptase-polymerase chain reaction. Although 85% of the synovial sarcomas studied demonstrated t(X;18), 75% of the malignant peripheral nerve sheath tumors in our cohort also demonstrated this translocation. We conclude that the translocation t(X;18) is not specific to synovial sarcoma and discuss the implications of the demonstration of t(X;18) in a majority of malignant peripheral nerve sheath tumors.</abstract><cop>New York</cop><pub>Elsevier Inc</pub><doi>10.1038/modpathol.3880247</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Chromosomal translocation Erratum Laboratory Medicine malignant peripheral nerve sheath tumor Medicine Medicine & Public Health Pathology specificity synovial sarcoma t(X 18) |
title | Erratum: Malignant Peripheral Nerve Sheath Tumors with t(X;18). A Pathologic and Molecular Genetic Study |
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