炎性肌成纤维细胞瘤：一种罕见的仅累及胸膜的病例报告。
Inflammatory myofibroblastic tumour: report of a rare form with exclusive pleural involvement.
作者信息
Nobre de Jesus Gustavo, Rocha Sara Lemos, Lopes João Madeira, Santos João Meneses, Oliveira Pedro Soares, Victorino Rui M M
机构信息
Medicina 2, Hospital de Santa Maria/CHLN, Faculdade de Medicina da Universidade de Lisboa, Avenida Egaz Moniz, 1649-035 Lisboa, Portugal.
Departamento de Anatomia Patológica, Hospital da Luz, Avenida Lusiada, 1500-650 Lisboa, Portugal.
出版信息
Case Rep Pulmonol. 2014;2014:621941. doi: 10.1155/2014/621941. Epub 2014 Nov 26.
Inflammatory myofibroblastic tumour (IMT) is a rare scleroinflammatory lesion, characterized by a myofibroblastic proliferation with inflammatory infiltrates, with many possible locations and diagnosis based on immunohistochemistry. Pleural IMT is uncommon and is usually an extension of a pulmonary involvement. We report on a 28-year-old woman with a new form of this rare entity, characterized by exclusive pleural involvement.
炎性肌成纤维细胞瘤（IMT）是一种罕见的硬化性炎性病变，其特征为肌成纤维细胞增生伴炎性浸润，可发生于多种部位，依靠免疫组织化学进行诊断。胸膜IMT较为少见，通常是肺部病变的延伸。我们报告了一名28岁女性，患有这种罕见疾病的一种新形式，其特征为仅累及胸膜。
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