Key result
Incomplete resection of primary thyroid synovial sarcoma linked to repeated recurrences and worsening differentiation.
Why the study?
Primary synovial sarcoma of the thyroid is rare and tends to present poor biological behavior requiring tailored initial treatment to improve prognosis.
Case Report (n=1)
No
Incomplete initial surgical resection of primary thyroid synovial sarcoma can lead to rapid local recurrences with progressively poorer tumor differentiation.
Supports complete initial resection for rare primary thyroid synovial sarcoma; single case leaves open optimal adjuvant strategies.
The primary occurrence of synovial sarcoma (SS) in the thyroid is quite rare. As other SS arise from the head and neck structure, it tends to present poor biological behaviors and is generally treated as a high-grade sarcoma. The present study reports the case of a 31-year-old male who presented a neck mass, involving the thyroid, as shown by ultrasonography. The tumor was resected by total thyroidectomy and diagnosed as SS by histopathology. However, the initial surgery was considered as incomplete (R2) and no adjuvant protocol was followed. At the follow-up, neck recurrences within local lymph nodes were found repeatedly. The tumor grade increased for the metastatic lesions, indicating poorer differentiations with repeated relapses. The accurate evaluations of the primary tumor facilitated it to tailor the initial treatments, otherwise, the prognosis may be deteriorated by inappropriate management.
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Shi et al. (2016) conducted a case report in Primary synovial sarcoma of the thyroid (n=1). Total thyroidectomy was evaluated on Local recurrence and histological transformation. A 31-year-old male with primary synovial sarcoma of the thyroid experienced repeated local recurrences with increasingly poor differentiation following an initial incomplete surgical resection.
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