Abstract: Granular cell tumor of the vulva is a rare vulvar disease without typical clinical features. Preoperative diagnosis is extremely difficult. In this paper, we present a 34-year-old female who underwent local excision of vulvar nodules due to recurrent vulval pain. Because of the rarity in clinical gynecology, multidisciplinary consultation was organized to identify the benign or malignancy, and developed a postoperative follow-up program. The patient has not relapsed.

Key words: Vulvar neoplasms, Granular cell tumor, Pathology;, Diagnosis, Therapy, Case reports