Inflammatory Myofibroblastic Tumour of Lung, A Rare Entity

Bilal Umair, Sohail saqib, Rashid Husnain, R. Khan, F. Ullah
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Abstract

Inflammatory fibroblastic tumour of lung is a rare mesenchymal tumour usually affecting the children and young adults. It is usually considered as a benign entity however it has high potential for recurrence and local invasion. Exact pathogenesis of tumour is not known. Complete surgical excision is the treatment of choice. Due to high chance of recurrence, patients are usually kept on close follow up. Here we present a case of inflammatory myofibroblastic tumour of lung , who presented with history of pain and shortness of breath.She was diagnosed  a case of inflammatory myofibroblastic tumour with the help of CT scan chest and CT Guided biopsy.She underwent  right sided pneumonectomy and remained symptom free on follow up. Key Words. Inflammatory, Myofibroblasts, Pneumonectomy, Tumour.  
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肺炎性肌成纤维细胞瘤,一种罕见的肿瘤
肺炎性纤维母细胞瘤是一种罕见的间充质肿瘤,多见于儿童和青年。它通常被认为是一种良性实体,但它有很高的复发和局部侵袭的可能性。肿瘤的确切发病机制尚不清楚。完全的手术切除是治疗的选择。由于复发率高,患者通常保持密切随访。我们在此报告一例肺炎性肌纤维母细胞瘤,其表现为疼痛和呼吸短促。经胸部CT扫描及CT引导下活检诊断为炎性肌成纤维细胞瘤。她接受了右侧全肺切除术,并在随访中保持无症状。关键字。炎性,肌成纤维细胞,全肺切除术,肿瘤。
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发文量
35
审稿时长
16 weeks
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