Olscamp G, Weisbrod G, Sanders D, Delarue N, Mustard R
Radiology. 1980 Apr;135(1):43-8. doi: 10.1148/radiology.135.1.7360978.
Castleman disease was originally described in 1954 as a form of localized mediastinal lymph-node hyperplasia. It has also been reported as a solitary mass in the hilar region or peripheral lymph nodes. The authors describe 4 cases, 3 in the chest and 1 in the neck. The intrathoracic lesions involved (a) the middle portion of the superior mediastinum with extension into the neck, (b) the posterior paravertebral mediastinum with extension into the posterior intercostal spaces, and (c) the extrapleural posterior chest wall, respectively: this last case is unusual in that the tumor recurred in the same site several years after removal. The clinical, radiological, and pathological features are presented.
卡斯特曼病最初于1954年被描述为一种局限性纵隔淋巴结增生症。也有报道称其为肺门区或周围淋巴结的孤立性肿块。作者描述了4例病例，其中3例在胸部，1例在颈部。胸内病变分别累及：(a) 上纵隔中部并延伸至颈部；(b) 椎旁后纵隔并延伸至后肋间隙；(c) 胸膜外后胸壁：最后一例不寻常之处在于肿瘤在切除数年后于同一部位复发。本文呈现了其临床、放射学及病理学特征。
