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A case of retroperitoneal dedifferentiated liposarcoma initially diagnosed as malignant fibrous histiocytoma: a case report

机译:腹膜后去分化脂肪肉瘤一例初步诊断为恶性纤维组织细胞瘤:一例报告

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摘要

We report a case of retroperitoneal tumor which turned out to be liposarcoma by the histological evaluation of its recurrent tumor, although the initial tumor was diagnosed as malignant fibrous histiocytoma (MFH). A retroperitoneal tumor in a 62-year-old man was removed and pathologically diagnosed as MFH. Five years after the initial surgery, computed tomography (CT) demonstrated a recurrent tumor near the spleen. The tumor was resected together with the spleen, tail of pancreas, and connective tissue due to adhesion and diagnosed as well-differentiated liposarcoma with sclerosing component. Generally dedifferentiated liposarcoma is difficult to distinguish from MFH and the presence of a well-differentiated liposarcoma component in the adjacent adipose tissue leads to the diagnosis of dedifferentiated liposarcoma. The clinical course of the present case indicated that the initial tumor was dedifferentiated liposarcoma and the recurrent tumor developed from the surrounding well-differentiated liposarcoma.
机译:我们报告了一例腹膜后肿瘤,尽管其最初的肿瘤被诊断为恶性纤维组织细胞瘤(MFH),但通过其复发性肿瘤的组织学评估证明它是脂肪肉瘤。一名62岁男子的腹膜后肿瘤被切除,并经病理诊断为MFH。初次手术五年后,计算机断层扫描(CT)显示脾脏附近复发了肿瘤。由于粘附,将肿瘤与脾脏,胰腺尾巴和结缔组织一起切除,并诊断为具有硬化成分的分化良好的脂肪肉瘤。通常,去分化的脂肪肉瘤很难与MFH区别开来,并且在相邻的脂肪组织中存在高度分化的脂肪肉瘤成分会导致去分化的脂肪肉瘤的诊断。本病例的临床过程表明,最初的肿瘤是去分化的脂肪肉瘤,而复发的肿瘤是从周围的高度分化的脂肪肉瘤发展而来的。

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