Department of Respiratory Medicine, First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Int J Tuberc Lung Dis. 2015 Mar;19(3):362-5. doi: 10.5588/ijtld.14.0647.
Castleman disease (CD) is a rare reactive lymphoproliferative disorder, first identified in 1954. We recently had the opportunity to analyse the characteristics of two variations of CD with pulmonary involvement. Case 1 had localised retroperitoneal hyaline vascular type CD, while Case 2 was diagnosed as multicentric plasma cell type CD. Both patients had pulmonary symptoms and signs, including cough, dyspnoea, hypoxaemia and ventilatory dysfunction; however, they had different physiological manifestations of their pulmonary abnormalities.
血管滤泡性淋巴结增生症(CD)是一种罕见的反应性淋巴组织增生性疾病,于 1954 年首次被发现。我们最近有机会对两种伴有肺部受累的 CD 变体的特征进行了分析。病例 1 为局部腹膜后透明血管型 CD,而病例 2 被诊断为多中心浆细胞型 CD。两名患者均有肺部症状和体征,包括咳嗽、呼吸困难、低氧血症和通气功能障碍;然而,他们的肺部异常表现出不同的生理特征。