Key result
Wide surgical resection of a primary epithelioid sarcoma of the scalp resulted in no evidence of tumor recurrence at 36 months of follow-up.
Why the study?
Primary epithelioid sarcoma of the scalp is extremely rare and challenging to diagnose, largely due to a lack of literature on its imaging features.
Case Report (n=1)
Wide surgical resection of a rare primary scalp epithelioid sarcoma resulted in no recurrence at 36 months.
Supports wide resection for rare scalp epithelioid sarcoma; hypothesis-generating and requires validation in larger cohorts.
Primary epithelioid sarcoma is an extremely rare malignancy of the scalp. To date, less than a dozen such cases have been reported in the literature. The diagnosis often is a challenge to both radiologists and clinicians. This is largely attributed to the lack of literature on the imaging features of scalp epithelioid sarcoma. In this report, we highlight the role of multimodality imaging in the diagnosis of primary scalp epithelioid sarcoma and review the epidemiology, imaging, treatment options, and prognosis of these malignant scalp tumors. Displaying a multilobulated morphology, heterogeneous enhancement, and restricted diffusion on MRI, these tumors typically show central degeneration with hemorrhage, necrosis, and calcification. Wide surgical resection and adjuvant radiotherapy are the mainstays of treatment for localized scalp tumors. Nevertheless, the prognosis of patients with distant metastases at diagnosis is extremely poor compared to those with local or regional diseases.
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Zhang et al. (2021) conducted a case report in Primary epithelioid sarcoma of the scalp (n=1). Wide surgical resection and split skin graft was evaluated on Tumor recurrence. Wide surgical resection of a primary epithelioid sarcoma of the scalp resulted in no evidence of tumor recurrence at 36 months of follow-up.
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