A primitive neuroectodermal tumor (PENT) belongs to the category of a Ewing sarcoma. A PENT of the uterus is rare and has been known to be very aggressive by nature. Owing to the rarity of the tumor, there is no optimal treatment at present. In many cases, after hysterectomy, chemotherapy or radiation therapy has been performed. However, an effective chemotherapy regimen was unclear. In the soft tissue sarcoma area, the chemotherapy approach has recently greatly improved. Vincristine, doxorubicin, cyclophosphamide, ifosfamide and etoposide (VDC-IE) therapy has improved the survival rate of patients with Ewing sarcoma/PENT. Thus, VDC-IE therapy may be used for a uterine PENT. Here, we report a case of a uterine PENT in a premenopausal woman successfully treated with multimodality treatment including VDC-IE therapy and discuss the optimal chemotherapy for a uterine PENT through a literature review.
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http://dx.doi.org/10.1111/jog.13753 | DOI Listing |
Cureus
June 2024
Department of Pathology, Hospital AGEL Nový Jičín, Nový Jičín, CZE.
Desmoplastic small round cell tumor is a very rare soft tissue sarcoma with a bleak prognosis and short patient survival. The most common occurrence is in 20-30-year-old men. Our study presents the case report of a 40-year-old patient who was diagnosed with this sarcoma.
View Article and Find Full Text PDFCancer Treat Rev
March 2024
Children's Cancer Centre, The Royal Children's Hospital Melbourne, VIC 3000, Australia; Department of Paediatrics, The University of Melbourne, Parkville VIC 3052 Australia; Murdoch Children's Research Institute, Melbourne, Australia.
Case Rep Oncol Med
December 2023
Department of Cell Therapy and Applied Genomics, King Hussein Cancer Center, Amman, Jordan.
Sarcoma with genetic alteration is an exceptionally rare and emerging subtype of sarcoma. It is categorized into two types: -related gene fusions such as sarcomas and other -rearranged sarcoma and sarcomas with internal tandem duplication of genes such as infantile undifferentiated round cell sarcomas and primitive myxoid mesenchymal tumors of infancy. sarcomas predominantly arise in bone rather than soft tissue and exhibit a higher occurrence in children and adolescent males, whereas sarcomas with internal tandem duplication show a wider age range but usually arise in the first year of life.
View Article and Find Full Text PDFJ Pers Med
April 2023
Department of Pediatrics, Taipei Medical University Hospital, Taipei 110, Taiwan.
J Surg Oncol
July 2023
Department of Orthopedic Surgery, Mayo Clinic, Rochester, Minnesota, USA.
Purpose: Extraskeletal Ewing sarcoma (EES), is a rare soft tissue sarcoma. Treatment for EES commonly involves chemotherapy and surgical resection (ST) or less commonly combined chemotherapy, surgery, and radiotherapy (ST + RT). The purpose of the current study was to evaluate our institutional experience treating EES.
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