PDF(Pubmed)
Abstract：
Inflammatory myofibroblastic tumors (IMTs) of the lung are a rare type of mesenchymal tumors that tend to occur more in the lungs of children. They are extremely rare in adults. IMTs require extensive pulmonary resection because they are commonly locally invasive. The key to preventing recurrence is complete resection, and the prognosis is excellent after surgery. We report a case of a patient with an inflammatory pseudotumor of the lung. The patient is a 27-year-old female who presented with a dry cough. A chest radiograph and computed tomography showed a lesion in the left main bronchus and near-total left lung collapse. As surgery was necessary to establish the diagnosis, left pneumonectomy was performed followed by a histological examination of the surgical specimen which confirmed inflammatory pseudotumor.
摘要：
肺部的炎性肌纤维母细胞瘤（IMT）是一种罕见的间充质肿瘤，倾向于在儿童肺部发生更多。在成年人中极为罕见。IMT需要广泛的肺切除术，因为它们通常是局部侵入性的。防止复发的关键是完全切除,手术后预后良好。我们报告了一例肺部炎性假瘤患者。患者是一名27岁的女性，出现干咳。胸部X光片和计算机断层扫描显示左主支气管有病变，左肺几乎完全塌陷。因为手术是必要的，以确定诊断，进行左肺切除术,然后对手术标本进行组织学检查,证实是炎性假瘤.
