Key result
CT, MRI, and immunohistochemistry characterize a primary renal synovial sarcoma in a 48-year-old man.
This case report details the imaging and pathological characteristics of a rare primary renal synovial sarcoma.
Adds rare renal synovial sarcoma to imaging differentials; extends case literature but leaves management implications open.
: Synovial sarcomas (SS) are soft tissue neoplasms that usually occur in the vicinity of large joints. Herein, we present the case of a 48-year-old man with renal synovial sarcoma (RSS). The clinical manifestations, computed tomography (CT) scan and magnetic resonance imaging (MRI) features, microscopic characteristics, and immunohistochemical findings of this uncommon tumor are described.
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Kuai et al. (2019) studied this question. Primary renal synovial sarcoma in a 48-year-old man was characterized using computed tomography, magnetic resonance imaging, microscopic evaluation, and immunohistochemical analysis.
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