Pulmonary sarcomatoid carcinoma - pathohistological and immunohistochemical analysis, prognosis and complex treatment

L. Marinova, B. Yordanova, N. Evgeniev
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Abstract

The pulmonary sarcomatoid carcinoma (PSC) is extremely rarely lung neoplasm. A woman at the age of 55 with a local advanced pulmonary sarcomatoid carcinoma of the right lung and CT data on bilateral adrenal metastases and three brain metastases were established. Diagnosis is placed after bronchoscopy with biopsy and detailed pathochistological and immunohistochemical analysis. PSC is extremely malignant and with high risk of distant haematogenic metastases. This rare clinical case support the need for strict pathohistological and immunohistochemical analysis, a difficult pathohistological differential diagnosis with other primary malignant lung tumors and the assessment of complex treatment. In order to improve the healing results and survival of patients, timely diagnosis is required at early stage with surgical treatment and subsequent adjuvant chemotherapy and targetеd therapy after genetic analysis of surgery or biopsy tissue material.
肺肉瘤样癌的病理组织学及免疫组化分析、预后及综合治疗
肺肉瘤样癌(PSC)是极为罕见的肺肿瘤。本文报告一名55岁的女性,患有局部晚期右肺肉瘤样癌,CT资料显示双侧肾上腺转移和3个脑转移。诊断后放置支气管镜活检和详细的病理组织学和免疫组织化学分析。PSC是一种恶性肿瘤,具有远处血源性转移的高风险。这个罕见的临床病例支持需要严格的病理组织学和免疫组织化学分析,难以与其他原发性恶性肺肿瘤的病理鉴别诊断和复杂的治疗评估。为了提高患者的愈合效果和生存率,需要在早期及时诊断,进行手术治疗,并在手术或活检组织材料基因分析后进行辅助化疗和靶向治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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