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Author Credentials

Samantha A. Smith BS Nadim Bou Zgheib MD, FACOG Andrea M. Vallejos MD Jonathan D. Cuda MD

Author ORCID Identifier

https://orcid.org/0000-0001-8716-3264

DOI

10.33470/2379-9536.1294

Abstract

Leiomyosarcoma (LMS) of the vulva is rare. However it is the most common histologic subtype of vulvar sarcoma, accounting for approximately 1% of all vulvar malignancies. [1-8] Whether genetics and epigenetics play a role in pathogenesis is unclear. [1] The tumor is slow-growing with non-specific symptoms, has high metastatic potential, and follows a bimodal age distribution. [1-8] Diagnosis and prognosis are based upon immunohistochemical expression and criteria from early literature. [1,3,5-7] The most common therapeutic approach involves radical vulvectomy with lymph node resection. The value of adjuvant chemotherapy and radiation remains unknown. [1,3,5-8] Our case describes a 46-year-old Caucasian G2P2 female with LMS of the left labia.

Conflict(s) of Interest

The authors have no financial disclosures to declare and no conflicts of interest to report.

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