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多形性(“去分化型”)软骨肉瘤。1例经细针穿刺活检初步检查的病例报告。

Pleomorphic ("dedifferentiated") chondrosarcoma. Report of a case initially examined by fine needle aspiration biopsy.

作者信息

Dee S, Meneses M, Ostrowski M L, Murakami M, Horowitz M, Graf W

机构信息

Department of Pathology, University of Florida Health Science Center, Jacksonville 32209.

出版信息

Acta Cytol. 1991 Jul-Aug;35(4):467-71.

PMID:1927183
Abstract

Fine needle aspiration (FNA) biopsy of a predominantly radiolucent, destructive lesion of the right distal femoral metaphysis of a 69-year-old man produced smears containing spindle-shaped cells with cytologic features consistent with a malignant fibrous histiocytoma. This initial diagnosis was supported by immunoperoxidase staining, which was strongly positive for vimentin and alpha-1-antichymotrypsin, focally positive for S-100 protein and negative for desmin, muscle-specific actin, keratin, carcinoembryonic antigen and epithelial membrane antigen. Subsequent surgical resection revealed a lesion with a predominance of malignant fibrous histiocytoma-type regions; however, focal microscopic areas contained a low-to-medium-grade cartilaginous component. The final diagnosis rendered was thus pleomorphic or so-called "dedifferentiated" chondrosarcoma. This rare lesion should be included in the differential diagnosis of malignant spindle-cell lesions of bone assessed by FNA biopsy.

摘要

对一名69岁男性右股骨远端干骺端主要为透射线的破坏性病变进行细针穿刺抽吸(FNA)活检,涂片显示有梭形细胞,其细胞学特征与恶性纤维组织细胞瘤一致。免疫过氧化物酶染色支持这一初步诊断,波形蛋白和α-1抗糜蛋白酶呈强阳性,S-100蛋白局灶阳性,结蛋白、肌肉特异性肌动蛋白、角蛋白、癌胚抗原和上皮膜抗原呈阴性。随后的手术切除显示病变主要为恶性纤维组织细胞瘤型区域;然而,局灶性显微镜下区域含有低至中等级别的软骨成分。因此最终诊断为多形性或所谓的“去分化”软骨肉瘤。这种罕见病变应纳入通过FNA活检评估的骨恶性梭形细胞病变的鉴别诊断中。

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