Joseph M G, Colby T V, Swensen S J, Mikus J P, Gaensler E A
Department of Pathology, St. Joseph's Health Centre, London, Ontario, Canada.
Mayo Clin Proc. 1990 Feb;65(2):192-7. doi: 10.1016/s0025-6196(12)65014-9.
We describe two adults with multiple cystic fibrohistiocytic tumors of the lung that manifested as bilateral nodular opacities, cystic lesions, or both on chest roentgenograms. One patient had recurrent episodes of pneumothorax and intermittent shortness of breath; the other was asymptomatic. Open-lung biopsy specimens showed identical histologically benign fibrohistiocytic proliferations associated with formation of cysts that were lined by metaplastic bronchiolar, squamous, or type II alveolar epithelium and old hemorrhage in the cysts. In both patients, the lesions grew slowly over a period of years. These unusual multiple bilateral fibrohistiocytic tumors of the lung should be included in the differential diagnosis of bilateral cystic lesions in the lung.
我们描述了两名患有肺部多发性囊性纤维组织细胞瘤的成年人,其在胸部X线片上表现为双侧结节状混浊、囊性病变或两者兼有。一名患者反复出现气胸发作和间歇性呼吸急促;另一名患者无症状。开胸肺活检标本显示,组织学上为相同的良性纤维组织细胞增生,伴有囊肿形成,囊肿内衬化生的细支气管、鳞状或II型肺泡上皮,且囊肿内有陈旧性出血。在两名患者中,病变在数年时间里缓慢生长。这些不寻常的双侧多发性肺部纤维组织细胞瘤应列入肺部双侧囊性病变的鉴别诊断中。