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肺炎性肌纤维母细胞瘤的临床及病理特征

张春荣 樊怿辉 谢鹏飞 施民新

中国临床医学2012,Vol.19Issue(4):360-361,2.
中国临床医学2012,Vol.19Issue(4):360-361,2.

肺炎性肌纤维母细胞瘤的临床及病理特征

Clinicopathological Features of Inflammatory Myofibroblastic Tumor of the Lung

张春荣 1樊怿辉 1谢鹏飞 1施民新1

作者信息

  • 1. 江苏省南通市肿瘤医院胸外科,江苏南通226361
  • 折叠

摘要

Abstract

Objective: To study the clinical, pathological and immunohistochemical features of inflammatory myofibroblastic tumor (IMT) of the lung. Methods:Three patients with IMT of the lung have been enrolled. Chest radiograph and computed tomography of the chest revealed two masses in the left upper lobe and one mass in the right upper lobe. All the 3 cases underwent pulmonary lobectomy and local lymph nodes dissection. Results; All masses have been resected successfully. No intraop-erative or perioperative complications occurred. Smooth muscle actin (SMA) were positive in all cases. Conclusions: Complete surgical resection of inflammatory myofibroblastic tumor of the lung is usually curative, but local recurrence may occur years after the surgery, therefore clinical follow-up is necessary.

关键词

/炎性肌纤维母细胞瘤/手术/免疫组化

Key words

Lung/ Inflammatory myofibroblastic tumor/ Surgical resection/ Immunohistochemistry

分类

医药卫生

引用本文复制引用

张春荣,樊怿辉,谢鹏飞,施民新..肺炎性肌纤维母细胞瘤的临床及病理特征[J].中国临床医学,2012,19(4):360-361,2.

中国临床医学

OACSTPCD

1008-6358

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