Extraskeletal Ewing's sarcoma: An adrenal localization
نویسندگان
چکیده
منابع مشابه
Primary Extraskeletal Ewings Sarcoma of Ala of Nose . 1
Extra skeletal Ewing's sarcoma is often described as a tumour involving the soft tissues of the lower extremities and the para vertebral region. Ewing's sarcoma presents a rare tumour of the head and neck, and even rarer in the nasal cavity and/or paranasal sinuses. Primary Ewing’s sarcoma of the ala of the nose has not been commonly described previously in the English literature. We present a ...
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Ewing sarcoma is most commonly a bone tumour which has usually extended into the soft tissues at the time of diagnosis. Exceptionally, this tumour can have an extraskeletal origin. Clinical or imaging findings are non-specific and diagnosis is based on histology. We report a case of an extraskeletal Ewing sarcoma developed in the soft tissues of the abdominal wall in a 35-year-old woman who pre...
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Extraskeletal Ewing's Sarcoma/Primitive Neuroectodermal Tumor presenting as a breast mass is uncommon. It may pose a diagnostic challenge. In order to increase awareness and identify potential diagnostic pitfalls, we report a 24 year-old woman extraosseous Extraskeletal Ewing's Sarcoma/Primitive Neuroectodermal Tumor arising in the breast.
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Primary malignant sarcomas of the spine are extremely rare. Because of biological heterogeneity, these tumors have variable sensitivity to radiation and chemotherapy. Adequate local control through complete tumor removal is an important therapeutic goal. However, aggressive resection of tumors in the spinal column must be coupled with restoration of spinal column stability and minimization of n...
متن کامل18q-syndrome and extraskeletal Ewing's sarcoma.
Cytogenetic studies carried out in a boy with multiple congenital anomalies showed a partial deletion of the long arm of chromosome 18. The child later developed an extraskeletal Ewing's sarcoma. The possible association of the tumour with 18q- syndrome is discussed.
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ژورنال
عنوان ژورنال: International Journal of Case Reports and Images
سال: 2016
ISSN: 0976-3198
DOI: 10.5348/ijcri-2016134-cr-10722