Nicholson A G, Wotherspoon A C, Diss T C, Singh N, Butcher D N, Pan L X, Isaacson P G, Corrin B
Department of Histopathology, Royal Brompton Hospital, London, UK.
Histopathology. 1996 Oct;29(4):317-24. doi: 10.1111/j.1365-2559.1996.tb01415.x.
Lymphomatoid granulomatosis is currently classified as part of a spectrum of angiocentric immunoproliferative lesions. These were initially thought to be of T-cell phenotype, but recent papers have shown that some cases are B-cell proliferations, sometimes associated with Epstein-Barr virus infection. We reviewed the clinicopathological features of 16 patients with pulmonary lymphomatoid granulomatosis, using immunohistochemistry to assess the phenotype of the infiltrate, the polymerase chain reaction to look for immunoglobulin heavy chain and T-cell receptor gene rearrangements, and in-situ-hybridization to look for Epstein-Barr virus infection. In seven of seven cases the atypical lymphoid population was of B-cell phenotype, with four cases showing evidence of either monoclonality or oligoclonality. All seven cases, including those that lacked unequivocal proof of malignancy, behaved aggressively. Epstein-Barr virus RNA was detected in four cases. We conclude that some cases of lymphomatoid granulomatosis are B-cell lymphomas, sometimes associated with Epstein-Barr virus infection.
淋巴瘤样肉芽肿病目前被归类为血管中心性免疫增殖性病变谱的一部分。这些病变最初被认为是T细胞表型,但最近的论文表明,一些病例是B细胞增殖,有时与爱泼斯坦-巴尔病毒感染有关。我们回顾了16例肺部淋巴瘤样肉芽肿病患者的临床病理特征,采用免疫组织化学评估浸润细胞的表型,聚合酶链反应检测免疫球蛋白重链和T细胞受体基因重排,原位杂交检测爱泼斯坦-巴尔病毒感染。在7例病例中,非典型淋巴细胞群体为B细胞表型,4例显示单克隆性或寡克隆性证据。所有7例病例,包括那些缺乏明确恶性证据的病例,病情进展迅速。4例检测到爱泼斯坦-巴尔病毒RNA。我们得出结论,一些淋巴瘤样肉芽肿病病例是B细胞淋巴瘤,有时与爱泼斯坦-巴尔病毒感染有关。