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Updated: May 1, 2026

In Vivo, Percutaneous, Needle Based, Optical Coherence Tomography of Renal Masses
Published on: March 30, 2015
Primary renal synovial sarcoma: computed tomography imaging findings.
Xiao-Fei Lv1, Ying-Wei Qiu2, Lu-Jun Han1
1Imaging and Interventional Radiology, Sun Yat-sen University Cancer Center; State Key Laboratory of Oncology in South China; Collaborative Innovation Center for Cancer Medicine, Guangzhou, PR China.
Primary renal synovial sarcomas (PRSSs) are rare kidney tumors. CT scans reveal them as solid-cystic masses with specific enhancement patterns, aiding in diagnosis for young adults.
Area of Science:
- Oncology
- Radiology
- Medical Imaging
Background:
- Synovial sarcoma of the kidney is exceptionally rare, with limited data on its imaging characteristics.
- Accurate radiological identification is crucial for timely diagnosis and treatment.
Purpose of the Study:
- To delineate the characteristic computer tomography (CT) findings of primary renal synovial sarcomas (PRSSs).
Main Methods:
- Retrospective analysis of five histopathologically and cytogenetically confirmed PRSS cases.
- Evaluation of unenhanced and multiphase enhanced CT scans for tumor morphology, size, margins, attenuation, and enhancement patterns.
Main Results:
- Tumors presented as solid-cystic masses with well-defined borders, cyst walls, or pseudo-capsules.
- Heterogeneous enhancement with a "rapid wash-in and slow wash-out" pattern was observed in the solid components.
- Renal vein and inferior vena cava thrombus occurred in one case; lymphadenopathy was absent.
Conclusions:
- PRSS should be considered in the differential diagnosis of renal neoplasms in adolescents and young adults.
- Key CT features include solid-cystic appearance, well-defined borders, cystic wall/pseudo-capsule, heterogeneous/septate enhancement, and specific enhancement kinetics.
- Absence of lymphadenopathy is a notable feature.
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