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Carvajal, R. and Meyers, P. (2005) Ewing’s Sarcoma and Primitive Neuroectodermal Family of Tumors. Hematology/Oncology Clinics of North America, 19, 501-525.
https://doi.org/10.1016/j.hoc.2005.03.004

has been cited by the following article:

• TITLE: Primary Vulvar Ewing Sarcoma in a 30-Year-Old Woman: A Case Report

  AUTHORS: Fatoumata Matokoma Sidibe, Hajar Ouahbi, Rajae Kanab, Layla Tahiri, Fatim Zhara El Mrabet, Samia Arifi, Hind El Fatemi, Nawfel Mellas

  KEYWORDS: Ewing Sarcoma/Primitive Neuroectodermal Tumor, Vulva, Advanced Disease, Multimodal Treatment

  JOURNAL NAME: Case Reports in Clinical Medicine, Vol.7 No.3, March 21, 2018

  ABSTRACT: Primary Ewing sarcoma (ES) and primitive neuroectodermal tumor (PNET) are considered as Ewing sarcoma family of tumors (ESFT), characterized by chromosomal translocation t(11; 22) (q24; q12) leading to a chimeric transcript EWS-FLI1 in 85% of cases. It typically involves the soft tissues of the chest wall, pelvis, paravertebral region, abdominal wall, retroperitoneal region and extremities in children, adolescents and young adults. It rarely occurs in the female genital tract. We report an extremely rare case of advanced vulvar Ewing sarcoma/PNET of the vulva confirmed by Fluorescence In Situ Hybridization (FISH) in a 30-year-old woman. The patient was treated by 6 cycles of chemotherapy followed by radiotherapy with favourable outcome.