Primary intrathoracic synovial sarcoma: a clinicopathologic study of 40 t(X;18)-positive cases from the French Sarcoma Group and the Mesopath Group

Details

Serval ID
serval:BIB_5161EAE8A208
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Primary intrathoracic synovial sarcoma: a clinicopathologic study of 40 t(X;18)-positive cases from the French Sarcoma Group and the Mesopath Group
Journal
American Journal of Surgical Pathology
Author(s)
Begueret  H., Galateau-Salle  F., Guillou  L., Chetaille  B., Brambilla  E., Vignaud  J. M., Terrier  P., Groussard  O., Coindre  J. M.
ISSN
0147-5185 (Print)
Publication state
Published
Issued date
2005
Volume
29
Number
3
Pages
339-346
Notes
PT - Journal Article PT - Research Support, Non-U.S. Gov't
Abstract
Synovial sarcoma (SS), an aggressive neoplasm accounting for up to 14% of soft tissue sarcomas, was recently recognized as a primary tumor in the lung and pleura. SS is characterized by the chromosomal translocation t(X;18)(SYT-SSX) found in more than 95% of the tumors. We report a cooperative study from the French Sarcoma Group and the Mesopath Group on 40 t(X;18)(SYT-SSX)-positive primary intrathoracic SS. There were 22 males and 18 females, whose age ranged from 16 to 79 years (median, 47 years). Neoplasms were mostly circumscribed and of large size (median, 7.5 cm; range, 2-16 cm). Thirty-nine tumors were monophasic SS, including 24 (60%) monophasic fibrous and 15 (37.5%) poorly differentiated cases, and one lesion was a biphasic SS. A larger proportion of poorly differentiated tumors were observed among intrathoracic SS as compared with soft tissue SS. Immunohistochemically, 90% of the cases reacted with at least one epithelial marker. CD34 was focally expressed in 3 cases. SYT-SSX1 fusion transcripts were detected in 22 cases (56.4%) and SYT-SSX2 fusion transcripts in 17 cases. Median and 5-year disease-specific survival in 33 patients was 50 months and 31.6%. Median and 5-year disease-free survival was 24 months and 20.9%. Patient sex, age, tumor size, histologic subtype, grade, and SYS-SSX fusion type had no significant impact on outcome. In conclusion, intrathoracic SS are rare but aggressive tumors with poor prognosis. In this unusual location, the detection of SYT-SSX fusion transcripts is a valuable diagnostic adjunct
Keywords
Adolescent/Adult/Aged/Chromosomes,Human,Pair 18/Chromosomes,Human,X/Female/Humans/Immunoenzyme Techniques/Male/Middle Aged/Oncogene Proteins,Fusion/analysis/Sarcoma,Synovial/chemistry/genetics/secondary/Soft Tissue Neoplasms/Pathology/Thoracic Neoplasms/Translocation,Genetic/Tumor Markers,Biological
Pubmed
Web of science
Create date
29/01/2008 18:33
Last modification date
20/08/2019 14:07
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