Joseph R, Chacko B, Manipadam M T, Sureka J, Cherian V K, John G T
Department of Nephrology, Christian Medical College, Vellore, India.
Transpl Infect Dis. 2008 Feb;10(1):52-5. doi: 10.1111/j.1399-3062.2007.00234.x. Epub 2007 May 19.
Lymphomatoid granulomatosis (LYG) is a rare multisystemic angiocentric lymphoproliferative disease, which can masquerade as necrotic tissue. There is a paucity of reports of LYG in renal transplant recipients. Herein, we describe LYG in a 56-year-old renal allograft recipient 11 years after transplantation, on azathioprine and prednisolone maintenance immunosuppression, presenting to us with fever, weight loss, and nodular and patchy opacities in both lung fields. Initial percutaneous samples showed necrotic tissue while open biopsy revealed characteristic histopathology with evidence of Epstein-Barr virus. We have reviewed the radiological and pathological findings, and discussed clinical features, differential diagnosis, and treatment of LYG.
淋巴瘤样肉芽肿病(LYG)是一种罕见的多系统血管中心性淋巴增殖性疾病,可表现为坏死组织。肾移植受者中关于LYG的报道较少。在此,我们描述了一名56岁的肾移植受者,在移植11年后,接受硫唑嘌呤和泼尼松龙维持免疫抑制治疗,出现发热、体重减轻以及双肺野结节状和斑片状阴影。最初的经皮穿刺样本显示为坏死组织,而开放活检显示出具有爱泼斯坦-巴尔病毒证据的特征性组织病理学表现。我们回顾了影像学和病理学发现,并讨论了LYG的临床特征、鉴别诊断和治疗。