Abstract
Background: Spindle cell rhabdomyosarcoma (SC-RMS) is a rare and recently described variant of rhabdomyosarcoma. It was previously considered a subtype of embryonal rhabdomyosarcoma (ERMS) but spindle cell and sclerosing rhabdomyosarcomas are now described separately in the 2013 World Health Organisation (WHO) classification.1 In adults, SC-RMS is most common in the head and neck region with a 40–50% rate of recurrence and metastasis.
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