Key result
Excision, chemotherapy, and radiation yield no 3-year recurrence and excellent hand function in median nerve sarcoma.
Why the study?
Intraneural synovial sarcoma of the median nerve is extremely rare with limited reported cases and outcomes.
Does excision followed by chemotherapy and radiation improve outcomes in a 15-year-old male with intraneural synovial sarcoma of the median nerve?
Case Report (n=1)
Does excision followed by chemotherapy and radiation improve outcomes in a 15-year-old male with intraneural synovial sarcoma of the median nerve?
Excision followed by chemotherapy and radiation resulted in a 3-year recurrence-free survival with excellent hand function in a rare case of intraneural synovial sarcoma of the median nerve.
Supports multimodal limb salvage in rare pediatric intraneural sarcoma; hypothesis-generating and requires validation before practice change.
There have been 8 synovial sarcomas of the median nerve reported. We report a case of a 15-year-old male with synovial sarcoma of the right-hand median nerve. Patient presented with a 2-month history of enlarging mass at the base of the right thenar eminence associated with numbness in the median nerve distribution. Physical examination revealed a soft mass over the thenar eminence and paresthesia in the median nerve distribution. He underwent excision of the tumor, which revealed a well-encapsulated lesion encompassing the median nerve, involving the first, second, and radial aspect of the third web space as well as recurrent branches of the median nerve. Following excision of the tumor, a thorough metastatic workup was negative for metastatic disease. He was staged as III, T2b, N0, M0-poorly differentiated monophasic synovial sarcoma of the right median nerve. Postoperatively the patient was started on chemotherapy and radiation. Intraneural synovial sarcoma is extremely rare. Our case is the youngest with the longest follow-up. He is currently at a status of 3 years posttreatment with no signs of recurrence and excellent use of his right hand. This case is of particular interest due to the rarity of the disease along with this being the best outcome reported in the literature to-date.
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Samia et al. (2021) conducted a case report in Intraneural synovial sarcoma of the median nerve (n=1). Tumor excision, chemotherapy, and radiation was evaluated on Recurrence and hand function. Tumor excision, chemotherapy, and radiation for intraneural synovial sarcoma of the median nerve in a 15-year-old male resulted in no recurrence and excellent hand function at 3 years.
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