Ekinci Gulbanu Horzum, Haciomeroglu Osman, Sen Ay Ccedil Im, Alpay Levent, Guney Pinar Atagun, Yilmaz Adnan
Department of Pulmonology, Sureyyapasa Center for Chest Diseases and Thoracic Surgery Training and Investigation Hospital, Istanbul, Turkey.
Department of Pathology, Sureyyapasa Center for Chest Diseases and Thoracic Surgery Training and Investigation Hospital, Istanbul, Turkey.
J Coll Physicians Surg Pak. 2016 Apr;26(4):331-3.
Inflammatory myofibroblastic tumor of the lung is a rare condition, with a reported incidence between 0.04 - 1.2% of all tumors of the lung. We present a case of inflammatory myofibroblastic tumor of the lung. A61-year man presented to the outpatient department complaining of cough and blood-streaked sputum for 5 days. The computed tomography scan of the chest demonstrated a 4.5 x 4 cm, calcified pulmonary mass in the anterior segment of the right upper lobe. Bronchoscophy and computed tomography-guided transthoracic fine needle aspiration was inconclusive. The tumor was removed via wedge resection. Histological and immunohistochemical findings were consistent with inflammatory myofibroblastic tumor of the lung.
肺炎性肌纤维母细胞瘤是一种罕见疾病,据报道其发病率占所有肺部肿瘤的0.04 - 1.2%。我们报告一例肺炎性肌纤维母细胞瘤病例。一名61岁男性因咳嗽和痰中带血5天就诊于门诊。胸部计算机断层扫描显示右上叶前段有一个4.5×4厘米的钙化肺肿块。支气管镜检查和计算机断层扫描引导下经胸细针穿刺活检结果不明确。通过楔形切除术切除肿瘤。组织学和免疫组化结果与肺炎性肌纤维母细胞瘤相符。