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[去分化脂肪肉瘤。6例临床病理研究]

[Dedifferentiated liposarcoma. A clinico-pathologic study of 6 cases].

作者信息

Coindre J M, de Loynes B, Bui N B, Stockle E, de Mascarel I, Trojani M

机构信息

Laboratoire d'Anatomie Pathologique, Fondation Bergonié, Bordeaux.

出版信息

Ann Pathol. 1992;12(1):20-8.

PMID:1580936
Abstract

During a period of 15 years, 6 cases of dedifferentiated liposarcomas were found among 542 cases of adult soft tissue sarcomas, 77 of which were liposarcomas. They were huge tumors of the retroperitoneum, containing distinct areas of well-differentiated liposarcoma most often of sclerosing type and malignant fibrous histiocytoma or undifferentiated sarcoma most often of high grade malignancy. Immunohistochemistry on the dedifferentiated component showed a positivity with anti-vimentin and alpha-1-antichymotrypsin in 5 cases and with anti-alpha smooth muscular actin in 4 cases. Three patients developed local recurrence and a fourth one quickly died with bone metastasis. Other types of dedifferentiated sarcomas, the process of dedifferentiation and links between malignant fibrous histiocytoma and dedifferentiated sarcomas are discussed.

摘要

在15年期间,在542例成人软组织肉瘤中发现6例去分化脂肪肉瘤,其中77例为脂肪肉瘤。它们是腹膜后巨大肿瘤,包含明显的高分化脂肪肉瘤区域,最常见的是硬化型,以及恶性纤维组织细胞瘤或未分化肉瘤,最常见的是高级别恶性肿瘤。对去分化成分进行免疫组织化学检测,5例显示抗波形蛋白和α-1抗胰凝乳蛋白酶呈阳性,4例显示抗α平滑肌肌动蛋白呈阳性。3例患者出现局部复发,第4例患者很快死于骨转移。文中还讨论了其他类型的去分化肉瘤、去分化过程以及恶性纤维组织细胞瘤与去分化肉瘤之间的联系。

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