Walter M, Thomson N M, Dowling J, Fox R, Atkins R C
Aust N Z J Med. 1979 Aug;9(4):434-6. doi: 10.1111/j.1445-5994.1979.tb04175.x.
Lymphomatoid granulomatosis is a multi-system disorder of high mortality and characterised by angiocentric and angiodestructive lymphoreticular proliferative and granulomatous change. A case is described of this disease occurring in a renal transplant patient. The patient underwent a rapid remission of the disease after a course of combined cytotoxic therapy and remains free of disease three years after treatment. This case is the second described renal transplant patient to develop the disease and the first to be successfully treated. It is likely that the disease originated as a consequence of immunosuppression similar to the development of lymphomas in allograft recipients.
淋巴瘤样肉芽肿病是一种死亡率很高的多系统疾病，其特征为血管中心性和血管破坏性淋巴网状细胞增生及肉芽肿性改变。本文描述了一例发生在肾移植患者身上的该疾病病例。该患者在接受了一个疗程的联合细胞毒性治疗后疾病迅速缓解，治疗三年后仍无疾病复发。此病例是第二例被描述的发生该疾病的肾移植患者，也是第一例成功治疗的患者。该疾病很可能是免疫抑制的结果，类似于同种异体移植受者中淋巴瘤的发生。
