肺炎性肌纤维母细胞瘤：一种罕见的实体瘤。
Inflammatory myofibroblastic tumor of the lung: A rare entity.
作者信息
Braham Yosra, Migaou Asma, Njima Manel, Achour Asma, Ben Saad Ahmed, Cheikh Mhamed Saoussen, Fahem Nesrine, Rouatbi Naceur, Joobeur Samah
机构信息
Pulmonology Department, Fattouma Bourguiba Hospital, Monastir, Tunisia.
Pathology Department, Fattouma Bourguiba Hospital, Monastir, Tunisia.
出版信息
Respir Med Case Rep. 2020 Nov 11;31:101287. doi: 10.1016/j.rmcr.2020.101287. eCollection 2020.
Inflammatory myofibroblastic tumor (IMT) is a rare mesenchymal tumor usually seen within the first and second decade. They are extremely rare in adults, constituting less than 1% of adult lung tumors. It's usually benign, but it had a tendency for local recurrence. We report a case of asymptomatic inflammatory myofibroblastic tumor of lung in a 46-year-old non-smoker woman.
炎性肌纤维母细胞瘤（IMT）是一种罕见的间叶性肿瘤，通常见于第一和第二个十年。在成年人中极为罕见，占成人肺部肿瘤的比例不到1%。它通常是良性的，但有局部复发的倾向。我们报告一例46岁不吸烟女性的无症状肺部炎性肌纤维母细胞瘤病例。
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