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Inflammatory Myofibroblastic Tumour (IMT) is a rare neoplasm of mesenchymal origin, most commonly seen in the lungs of children and adolescents, but it can occur in older persons also. IMT also called inflammatory pseudotumor accounts for less than 1% of all lung tumours. Approximately half of the patients are asymptomatic. However, the patients with symptoms show cough, haemoptysis, dyspnoea and chest pain. Biopsy by thoracotomy or video assisted thoracoscopic surgery is often necessary todoi:10.18203/2349-3933.ijam20150559 fatcat:l5aniyyshrg6xg5ejrxt2kqzty