eMedicine Specialties > Orthopedic Surgery > Neoplasms
Synovial Cell Sarcoma: Workup
Updated: Aug 7, 2008
Workup
Laboratory Studies
- Other than molecular diagnostic tests (see below), no laboratory studies are specific for this diagnosis.
Imaging Studies
- Plain radiographs may aid in the diagnosis, as synovial sarcoma typically produces a spotty calcification (snowstorm) within the matrix of the soft tissue tumor that may be visualized on plain radiographs (see Image 1).
- CT scanning is used to confirm the presence of a mass, its size, and its location, but it is nondiagnostic. CT scan also may detect secondary bony involvement, which is not uncommon with larger synovial sarcomas. Synovial sarcoma is a malignant disease; therefore, CT scanning of the chest is mandatory to exclude metastatic disease.
- MRI is the investigation of choice for soft tissue sarcomas. Low signal intensity is observed on T1-weighted images (see Image 2), and high signal intensity is observed on T2-weighted images (see Image 3). The signal from the matrix is fairly homogeneous unless calcification is present.
Other Tests
- Cytogenetic analysis aids the physician in detecting the specific chromosomal translocation t(X;18)(p11;q11).13
- The chromosomal translocation produces either the SYT/SSX1 or SYT/SSX2 fusion gene, which can be identified by reverse transcriptase-polymerase chain reaction (RT-PCR) in tumor tissue and possibly in blood.9,10,14
Diagnostic Procedures
The histologic picture can be confused with many other round blue cell tumors. Cytogenetic analysis aids the physician in detecting the specific chromosomal translocation between chromosome 18 and chromosome X.13 This translocation produces either the SYT/SSX1 SYT/SSX2, or SYT/SSX4 fusion gene. Identification of this anomaly is obtained by reverse transcriptase-polymerase chain reaction (RT-PCR) in tumor tissue, with a sensitivity of 96% and specificity of 100%. Detection of fusion transcripts is possible by molecular diagnostic techniques in biopsy samples. Fluorescence in situ hybridization (FISH test) is less expensive than RT-PCR. It has been suggested as a good method of first choice.14 This method has a lower sensitivity than RT-PCR, but they are concordant in 76% of cases.
Histologic Findings
Macroscopically, the tumor is a grayish-white and often has a greasy feel. Histologic features of synovial sarcoma are identical in children and adults.
Three types have been described:
- In monophasic type there is a predominance of spindle cells, mixed with round cells. Cells are arranged in fascicles with a poorly defined cytoplasm. The monophasic variant does not have glandular areas.
- The biphasic type has a layer of columnar epithelium in addition to spindle cells. It consists of plump, round cells and spindle-shaped fibroblasts alternating with glandular-like areas that are lined by synovial-like cells and contain mucin.
- A third type, called poorly differentiated, has numerous mitosis, high cellularity, and tumor necrosis.
Staging
Staging requires local imaging with MRI. The most likely site of distant spread (the lungs) can be observed with CT scanning. Synovial sarcoma is a high-grade lesion.
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References
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Further Reading
Keywords
synovial cell sarcoma, synovial sarcoma, synovial cell, connective tissue tumor, connective tissue neoplasm, synovioma, malignant neoplasm, malignant tumor, joint tumors
Workup: Synovial Cell Sarcoma