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Primary pulmonary chondrosarcomas: a clinicopathologic study of 4 cases.

机译:原发性肺软骨肉瘤:4例临床病理研究。

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摘要

Malignant cartilaginous tumors of the lung are unusual, and although their occurrence has been reported in the literature in some cases, their separation from other benign cartilaginous tumors of the lung can be very difficult. Four cases of primary chondrosarcomas of the lung are presented. The patients are 2 men and 2 women between the ages of 51 and 69 years. Clinically, the most common symptoms were chest pain, dyspnea, and cough. Two tumors were centrally located, whereas 2 tumors were peripheral. Complete surgical resection was accomplished in all the patients. Histologically, 2 tumors were low grade of the hyaline type, whereas 2 tumors were predominantly myxoid chondrosarcomas. In the 2 myxoid chondrosarcomas immunohistochemical studies for keratin, desmin, smooth muscle actin, and CD31 were negative, whereas S-100 protein shows focal positive staining in both cases. Follow-up showed that one patient with low-grade tumor was alive and well at 36 months, whereas one patient with myxoid chondrosarcoma died 45 days after diagnosis because of surgical complications. Two additional patients were lost to follow-up. Our study highlights the ubiquitous distribution of chondrosarcomas and the histopathologic spectrum that these tumors may show when occurring in the lung.
机译:肺部恶性软骨肿瘤是罕见的,尽管在某些情况下已有文献报道其发生,但将其与其他肺部良性软骨肿瘤分开是非常困难的。介绍了四例肺原发性软骨肉瘤。患者为2名男性和2名女性,年龄在51至69岁之间。临床上,最常见的症状是胸痛,呼吸困难和咳嗽。两个肿瘤位于中心,而两个肿瘤位于周围。所有患者均完成了手术切除。在组织学上,有2个肿瘤是透明性的,但有2个肿瘤主要是粘液样软骨肉瘤。在2个黏液样软骨肉瘤的免疫组织化学研究中,角蛋白,结蛋白,平滑肌肌动蛋白和CD31均为阴性,而S-100蛋白在两种情况下均显示局灶性阳性染色。随访显示,一名低度肿瘤患者活着并在36个月时康复,而一名粘液样软骨肉瘤患者在诊断后45天因手术并发症死亡。另外两名患者失去随访。我们的研究突出了软骨肉瘤的普遍分布以及这些肿瘤在肺部发生时可能显示的组织病理学频谱。

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