Streem S B
J Urol. 1984 Jul;132(1):10-2. doi: 10.1016/s0022-5347(17)49440-7.
The management of genitourinary malacoplakia in renal transplant recipients has been unsatisfactory previously, as evidenced by an unacceptably high rate of graft loss and mortality. To optimize future management of this problem we studied 2 poorly recognized factors in the pathogenesis and prognosis of genitourinary malacoplakia in transplant recipients: 1) the probable role of azathioprine as the specific immunosuppressive agent responsible for the pathogenesis of malacoplakia, and 2) the importance of the localization of the disease and its impact on the ultimate prognosis. A new therapeutic regimen is suggested, which includes long-term antibiotics combined with an immediate modification of azathioprine therapy and early graft nephrectomy in selected cases with renal parenchymal involvement.
肾移植受者泌尿生殖系统软斑病的管理以前一直不尽人意,移植肾丢失率和死亡率高得令人无法接受就证明了这一点。为了优化对这一问题的未来管理,我们研究了移植受者泌尿生殖系统软斑病发病机制和预后中两个未得到充分认识的因素:1)硫唑嘌呤作为导致软斑病发病的特定免疫抑制剂的可能作用,以及2)疾病定位的重要性及其对最终预后的影响。我们提出了一种新的治疗方案,包括长期使用抗生素,同时立即调整硫唑嘌呤治疗方案,并对选定的有肾实质受累的病例早期进行移植肾切除术。