Nishizawa Tomotaka, Saraya Takeshi, Ishii Haruyuki, Goto Hajime
Department of Respiratory Medicine, Kyorin University School of Medicine, Mitaka, Japan.
BMJ Case Rep. 2014 Mar 14;2014:bcr2013202661. doi: 10.1136/bcr-2013-202661.
A 59-year-old, previously healthy man presented to our hospital, with a 3-month history of high fever, nocturnal sweating and exertional dyspnoea. Aggressive diagnostic procedures such as multiple random skin biopsies and transbronchial lung biopsy (TBLB) led to an antemortem diagnosis of intravascular large B-cell lymphoma (IVLBCL), which showed abundant CD20 atypical lymphocytes aggregated in lumina of small vessels. The 29 cases diagnosed with IVLBCL during their lifetime by TBLB were reviewed. Their clinical features included respiratory symptoms (hypoxaemia, dyspnoea and dry cough) and persistent fever. IVLBCL patients show various radiological patterns (ground glass opacities, multiple centrilobular nodules, interlobular septal thickening, interstitial shadows and thickening of bronchovascular bundles), suggesting lymphatic or haematological spread. Antemortem diagnosis of IVLBCL is difficult, but a multidisciplinary approach, with aggressive multiple random skin biopsies and/or TBLB, should be considered in patients with respiratory symptoms that are refractory to antibiotics or prednisolone treatment.
一名59岁、既往健康的男性因持续3个月的高热、盗汗及劳力性呼吸困难前来我院就诊。通过多次随机皮肤活检及经支气管肺活检(TBLB)等积极的诊断手段,生前确诊为血管内大B细胞淋巴瘤(IVLBCL),可见大量CD20非典型淋巴细胞聚集于小血管腔内。回顾了29例生前经TBLB诊断为IVLBCL的病例。其临床特征包括呼吸道症状(低氧血症、呼吸困难及干咳)及持续发热。IVLBCL患者表现出多种影像学特征(磨玻璃影、多发小叶中心结节、小叶间隔增厚、间质阴影及支气管血管束增粗),提示淋巴管或血液播散。IVLBCL的生前诊断较为困难,但对于抗生素或泼尼松龙治疗无效的呼吸道症状患者,应考虑采用多学科方法,积极进行多次随机皮肤活检和/或TBLB。