Stainer Anna, Faverio Paola, Bono Francesca, Pesci Alberto
University of Milan Bicocca, San Gerardo Hospital, Respiratory Unit.
Monaldi Arch Chest Dis. 2018 May 14;88(1):907. doi: 10.4081/monaldi.2018.907.
Primary lung lymphoma (PLL) is a rare type of lymphoma confined to the lung at the time of diagnosis. Pulmonary diffuse large B cells lymphoma (P-DLBCL) is the second most common type of PLL and it usually appears radiologically as solitary or multiple nodules or areas of consolidation. We present the case of a 63-year-old Caucasian male who developed severe acute respiratory failure and diffuse ground glass opacities (GGO) on chest computerized tomography. Diffuse GGO may be the radiological expression of very different diseases, ranging from infectious processes to interstitial lung diseases (ILDs) and neoplastic diseases. In our case, pneumonia and de novo ILD were initially considered given the symptoms and past medical history. However, bronchoscopy with trans-bronchial biopsies demonstrated the presence of P-DLBCL, despite an unusual radiological presentation and negative cytological analyses on bronchoalveolar lavage. In conclusion, P-DLBCL should be considered among the many differential diagnoses of diffuse GGO.
原发性肺淋巴瘤(PLL)是一种罕见的淋巴瘤类型,在诊断时局限于肺部。肺弥漫性大B细胞淋巴瘤(P-DLBCL)是第二常见的PLL类型,其影像学表现通常为孤立或多发结节或实变区域。我们报告一例63岁的白种男性病例,该患者出现严重急性呼吸衰竭,胸部计算机断层扫描显示弥漫性磨玻璃影(GGO)。弥漫性GGO可能是多种不同疾病的影像学表现,从感染性疾病到间质性肺疾病(ILD)和肿瘤性疾病。在我们的病例中,鉴于症状和既往病史,最初考虑为肺炎和新发ILD。然而,经支气管活检的支气管镜检查显示存在P-DLBCL,尽管其影像学表现不寻常且支气管肺泡灌洗的细胞学分析为阴性。总之,在弥漫性GGO的众多鉴别诊断中应考虑P-DLBCL。