Primary primitive neuroectodermal tumor of the cervix

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Abstract

Primary primitive neuroectodermal tumors (PNETs) are rare and high-grade malignant tumors that mostly occur in children and young adults. The most common sites are the trunk, limbs, and retroperitoneum. Herein, we present a case of a PNET involving the cervix uteri in a 27-year-old woman. The lesion showed characteristic histologic features of a PNET and was positive for the immunohistochemical markers cluster of differentiation (CD) 99, vimentin, neuron-specific enolase, neural cell adhesion molecule 1 (CD56), and CD117 (c-kit), further defining the tumor while helping to confirm PNET. The clinical Stage IIIB tumor was treated with chemotherapy and radiotherapy. © 2013 Li et al, publisher and licensee Dove Medical Press Ltd.

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Li, B., Ling, O., Han, X., Zhou, Y., Tong, X., Zhang, S., & Zhang, Q. (2013). Primary primitive neuroectodermal tumor of the cervix. OncoTargets and Therapy, 6, 707–711. https://doi.org/10.2147/OTT.S45889

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