Giant Retroperitoneal Sarcoma
نویسندگان
چکیده
Soft-tissue sarcomas are relatively rare with approximately 8,600 new cases annually and represent less than 1% of all n ew l y d i agnosed ma l i gnanc i e s . Retroperitoneal sarcomas are malignant tumours arising from mesenchymal cells, which are usually located in muscle, fat, and connective tissues. One-third of malignant tumours located in the retroperitoneum are sarcomas, and approximately 15% of soft tissue sarcomas
منابع مشابه
Giant retroperitoneal sarcoma.
0.1%–0.2% of all malignant tumours and about 15% of all sarcomas. Liposarcoma is the most common type of retroperitoneal sarcoma (41%), followed by leiomyosarcoma, malignant fibrous histiocytoma, fibrosarcoma and other undifferentiated sarcomas. We report the case of a woman with a giant retroperitoneal sarcoma and show that large tumour size is not necessarily a contraindication to surgical ex...
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Background. The concomitant occurrence of a renal cell carcinoma and retroperitoneal sarcoma is extremely rare with only few cases being reported. Methods. We present a case of simultaneous renal cell carcinoma and exceptionally large size retroperitoneal sarcoma involving small intestine. Surgical resection of retroperitoneal sarcoma and simultaneous right nephrectomy were performed. Results. ...
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Soft tissue sarcomas represent less than 1% of all human neoplasms. One-third of malignant tumors that arise in the retroperitoneum are sarcomas and liposarcoma is the most common retroperitoneal sarcoma. More often than not, patients report late to the hospital due to the slow progress and few late symptoms. Thus, the tumor is known to grow to enormous sizes. Here, we report a case of giant re...
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The differential diagnosis of retroperitoneal mass includes liposarcoma, leiomyosarcoma, malignant fibrous histiocytoma, neurofibroma, stromal tumor, teratoma, and lymphoma. Leiomyosarcoma is rare with poorer prognosis than other soft tissue sarcomas. Soft tissue sarcoma of retroperitoneal origin often remains asymptomatic until tumor enlargement, leading to diagnosis at advanced stages.
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Malignant fibrous histiocytoma, usually seen in patients older than 10 years, is an aggressive soft-tissue sarcoma occurring mostly in the extremities and the trunk, but it is extremely rare in children. We report the clinical, radiological and pathologic features of a five-year-old boy who was diagnosed as a retroperitoneally originated malignant fibrous histiocytoma. The patient with unresect...
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