primitive neuroectodermal tumor of the cervix uteri: a case report and review of literature
نویسندگان
چکیده
ewing’s sarcoma is a round cell malignancy of bone and soft tissue that occurs predominately in adolescents and young adults.it is an uncommon malignancy, but is recognized as the second most prevalent primary bone tumor worldwide. extraosseous ewing’s sarcoma is extremely rare and can affect the skin, soft tissues, or viscera. prognostic and therapeutic features of ewing’s extraosseous tumors are similar to those of ewing’s sarcoma. a primary ewing’s sarcoma arising from the cervix is highly rare. most of these patients presented with abnormal vaginal bleeding. we report a case of extraskeletal ewing’s sarcoma arising in the cervix in a 25-year-old woman.
منابع مشابه
Primitive neuroectodermal tumor of the cervix: a case report
INTRODUCTION Peripheral primitive neuroectodermal tumor of the cervix uteri is extremely rare. Between 1987 and 2010, there were only nine cases reported in the English literature, with considerably different management policies. CASE PRESENTATION A 45-year-old Iranian woman presented to our facility with a primitive neuroectodermal tumor of the cervix uteri. Her clinical stage IB2 tumor was ...
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Extraskeletal Ewing’s Sarcoma is a rare soft tissue tumor that is morphologically indistinguishable from the more common Ewing’s sarcoma of the bone. Primitive Ewing’s sarcoma of the breast is exceptionally reported. We present the case of a 26-year-old woman with Ewing sarcoma/PNET diagnosed by molecular biology showing the specific t ranscr ipt of Ewing/ per ipheral pr imi t ive neuroectoderm...
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عنوان ژورنال:
international journal of hematology-oncology and stem cell researchجلد ۶، شماره ۴، صفحات ۳۰-۳۲
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