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对一名4岁男孩的炎性肌纤维母细胞瘤进行完整手术切除并隆突重建。

Complete surgical resection of inflammatory myofibroblastic tumor with carinal reconstruction in a 4-year-old boy.

作者信息

Hoseok I, Joungho Han, Ahn Kang Mo, Lee Sang Il, Jhingook Kim

机构信息

Department of Thoracic and Cardiovascular Surgery, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul 135-710, Korea.

出版信息

J Pediatr Surg. 2005 Dec;40(12):e23-5. doi: 10.1016/j.jpedsurg.2005.08.043.

Abstract

Inflammatory myofibroblastic tumor of the carina and the main bronchus is a rare tumor. The authors report here on a case of a 4-year-old boy with an inflammatory myofibroblastic tumor at the carina and extending to the left main bronchus. He presented with fever and a cough of 2 months' duration. Preoperative assessment of the tumor revealed an intraluminal round mass arising from the carina and extending into the left main bronchus, and this caused near-total obstruction of the left main bronchus and the subsequent total collapse of the entire left lung. The complete resection of the mass with carinal reconstruction was successful. The tumor was a round mass measuring 1.5 x 1 cm. It had characteristic features of an inflammatory myofibroblastic tumor, namely, the proliferation of spindle-shaped fibroblasts and myofibroblasts.

摘要

隆突及主支气管炎性肌纤维母细胞瘤是一种罕见的肿瘤。作者在此报告一例4岁男孩,其隆突处患有炎性肌纤维母细胞瘤并延伸至左主支气管。他出现发热和持续2个月的咳嗽症状。术前对肿瘤的评估显示,一个腔内圆形肿物起源于隆突并延伸至左主支气管,这导致左主支气管几乎完全阻塞,随后整个左肺完全萎陷。成功地完整切除肿物并进行了隆突重建。肿瘤为一个大小为1.5×1厘米的圆形肿物。它具有炎性肌纤维母细胞瘤的特征性表现,即梭形成纤维细胞和肌成纤维细胞的增殖。

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