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Primary diffuse large B-cell lymphoma or lymphomatoid granulomatosis grade 3: \ud a still-puzzling diagnosis in autopsy

机译:原发性弥漫性大B细胞淋巴瘤或淋巴瘤样肉芽肿病3级:\ ud 尸检中仍然令人费解的诊断

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摘要

Primary lung lymphoma is a rare entity accounting for approximately 0.3% of\udall primary neoplasia of the lung and includes diffuse large B-cell lymphoma\ud(DLBL) and lymphomatoid granulomatosis (LYG). Considering that clinical\udfeatures may be similar, whereas epidemiology, morphology, and radiological\udfeatures are different, the authors report a case of a middle-aged man\udwho presented multiple pulmonary nodules in the lower lobes and groundglass\udopacities scattered bilaterally on computed tomography. Clinically, he\udpresented a consumptive syndrome with respiratory failure and pleurisy,\udwhich progressed until death. The autopsy findings were consistent with\udlymphomatoid granulomatosis (LYG) grade 3/ diffuse large B-cell lymphoma\ud(DLBL). The authors call attention to the difficulty of establishing an accurate\uddiagnosis, mainly when the demonstration of EBV-infected atypical B-cells\udfails.
机译:原发性肺淋巴瘤是一种罕见的实体,约占肺原发性肿瘤的0.3%,包括弥漫性大B细胞淋巴瘤ud(DLBL)和淋巴瘤样肉芽肿(LYG)。考虑到临床\特征可能相似,而流行病学,形态学和放射学\特征不同,作者报告了一个中年男子的病例,该人在下叶有多个肺结节,而在计算时双侧散布了玻璃\不透明断层扫描。在临床上,他表现为一种患有呼吸衰竭和胸膜炎的消耗性综合症,其发展一直持续到死亡。尸检结果与\ udmphomatoid肉芽肿病(LYG)3级/弥漫性大B细胞淋巴瘤\ ud(DLBL)一致。作者提请注意建立准确的\ ud诊断的困难,主要是在证明EBV感染的非典型B细胞\ udfails失败时。

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