Ansari S, Dubaybo H, Levi E, Dubaybo B A
Department of Internal Medicine, Wayne State University School of Medicine, 4201 St. Antoine, UHC-2E, Detroit, MI 48201, USA.
Case Rep Pulmonol. 2012;2012:146081. doi: 10.1155/2012/146081. Epub 2012 Aug 30.
We describe an unusual case of severe pulmonary bullous disease developing during treatment of marginal zone B-Cell lymphoma (MALT) involving the pulmonary parenchyma. The patient originally presented with pneumonia-like symptoms along with hemoptysis and was diagnosed with MALT lymphoma after a video-assisted thoracic surgical (VATS) lung biopsy. Computed tomography (CT) of the chest at diagnosis revealed multiple opacities, but no bullous disease. During the ensuing 4 years, and while on chemotherapy for the MALT lymphoma, sequential CT and pulmonary function tests revealed the development of progressive bullous disease resulting in the replacement of large portions of the lung parenchyma with bilateral bullae. This complication is rare, has been reported only once before in a patient with concomitant amyloidosis, and may be related to activation of proteolytic enzymes by lymphoma cells or chemotherapeutic agents.
我们描述了一例罕见病例,在治疗累及肺实质的边缘区B细胞淋巴瘤(MALT)期间发生了严重的肺大疱病。患者最初表现为类似肺炎的症状并伴有咯血,经电视辅助胸腔镜手术(VATS)肺活检后被诊断为MALT淋巴瘤。诊断时胸部计算机断层扫描(CT)显示有多个混浊影,但无大疱病。在随后的4年里,在接受MALT淋巴瘤化疗期间,连续的CT和肺功能测试显示进行性大疱病逐渐发展,导致双侧肺大疱取代了大部分肺实质。这种并发症很罕见,之前仅在一名伴有淀粉样变性的患者中报道过一次,可能与淋巴瘤细胞或化疗药物激活蛋白水解酶有关。