肺的炎性假瘤

Marina D. Petrovic , Miroslav S. Tomovic , Vesna D. Stankovic
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引用次数: 4

摘要

肺炎性假瘤(IPT)是一种罕见的良性肿瘤,实际上是炎症细胞的非肿瘤性无调节生长。虽然网状内皮细胞常见于浆细胞,但这类肿瘤常被描述为“浆细胞肉芽肿”。大多数病例累及肺和气道,然而,纵隔、胸淋巴结和其他结构很少受到影响(1)。这种来源不明的良性实体通常是局部侵入性的,需要广泛的肺切除术(2)。因为炎性假肿瘤在临床和影像学上都与恶性肿瘤相似,放射科医生应该熟悉这个实体,并在可能的情况下通过在鉴别诊断中包括假肿瘤来避免不必要的根治性手术(3)。放射检查结果和计算机断层扫描是区分恶性肿瘤的必要诊断程序。在IPT的临床过程中,已经描述了非常缓慢的生长、转化为肉瘤和消退(自发或在皮质类固醇治疗后)(4)。
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Inflammatory pseudotumor of the lungs

Inflammatory pseudotumor (IPT) of the lung is rare benign tumor which is in fact, nonneoplastic unregulated growth of inflammatory cells. Although plasma cells with reticuloendothelial elements are often seen, this kind of tumors is often described as a “plasma cell granuloma”. The lungs and airways are involved in the majority of cases, however, the mediastinum, thoracic lymph nodes and other structures are rarely affected (1). This benign entity of unknown origin is often locally invasive requiring extensive pulmonary resection (2). Because inflammatory pseudotumors mimic malignant tumors both clinically and radiologically, the radiologist should be familiar with this entity and help avoid unnecessary radical surgery when possible by including pseudotumor in the differential diagnosis (3). Radiographic findings as well as computed tomography are esential diagnostic procedures for malignancy distinction. Very slow growth, transformation to a sarcoma and regression (spontaneously or after corticosteroid therapy) have been described in the in clinical course of IPT (4).

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