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首页> 外文期刊>Pathology International >Primary giant cell malignant fibrous histocytoma of the lung: a case report.
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Primary giant cell malignant fibrous histocytoma of the lung: a case report.

机译:肺原发性巨细胞恶性纤维组织细胞瘤:一例报道。

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摘要

A rare case of malignant fibrous histiocytoma of giant cell type originating in the lung of a 46-year-old woman is presented. The patient complained of having a cough that had lasted for a few weeks. A chest X-ray photograph showed a tumor shadow on the left lung. Histological and cytological examination of the biopsy specimen revealed that the tumor was a kind of sarcoma. An operative procedure was selected because of tumor invasion into the trunk of the left pulmonary artery, which was discovered on computed tomography examination, and because metastatic tumor was excluded clinically. The tumor was almost encapsulated and 6 x 6 x 6 cm in size; however, it also showed invasion into the pulmonary artery and bronchial lumen. A histological survey of the tumor showed a wide range of patterns such as fibrous, pleomorphic, fascicular and osteoclast-like giant cell figures; however, the osteoclast-like giant cell area was predominant. Immunohistochemically, the tumor cells were positive for vimentin, CD68 for histiocytic marker and alpha1-antichymotrypsin, and negative for keratin, epithelial membrane antigen, S-100 protein, MT-1, desmin, myoglobin and lysosome. No primary tumor was found clinically in any part of the patient's body at 2 and 4 months after operation. Consequently, she was diagnosed as having primary giant cell malignant fibrous histiocytoma of the lung.
机译:罕见的恶性纤维组织细胞瘤的巨细胞类型起源于一名46岁妇女的肺部病例。病人抱怨咳嗽持续了几周。胸部X光照片显示左肺有肿瘤阴影。活检标本的组织学和细胞学检查显示,肿瘤是一种肉瘤。选择一种手术方法是因为肿瘤侵入了左肺动脉主干,这是在计算机断层扫描检查中发现的,并且由于临床上排除了转移性肿瘤。肿瘤几乎被包裹起来,大小为6 x 6 x 6 cm。然而,它也显示出侵入肺动脉和支气管腔。肿瘤的组织学检查显示了多种模式,例如纤维状,多形性,束状和破骨细胞样巨细胞形态。然而,破骨细胞样巨细胞区占主导。免疫组织化学检测,肿瘤细胞波形蛋白阳性,组织细胞标记物CD68和α1-抗胰凝乳蛋白酶阳性,角蛋白,上皮膜抗原,S-100蛋白,MT-1,结蛋白,肌红蛋白和溶酶体阴性。术后2个月和4个月,在患者身体的任何部位均未在临床上发现原发性肿瘤。因此,她被诊断为患有肺部原发性巨细胞恶性纤维组织细胞瘤。

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