A Case of Capd-Related Cryptococcus Peritonitis after Kidney Transplant Failure

M. Cabibbe, M. Querques, C. Brunati, M. Grotti, A. Montoli, G. Colussi
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Abstract

A 80-year-old man with severe atherosclerosis and chronic renal disease related to ischemic nephropathy gradually developed diabetes and uraemia six years after a kidney transplant. Immunosuppression included rapamycin 1 mg qd, mycophenolic acid 500 mg qd and prednisone 2.5 mg qd. When CAPD was started only low dose prednisone was maintained to preserve residual kidney function. Thirty days into CAPD, the patient presented with fever (38.4°C): the abdomen was tender, the PD catheter exit site was healthy, the peritoneal fluid was clear. Chest, abdomen and brain imaging were negative. He had blood (17.340/mm3,) and peritoneal fluid (190/mm3) leucocytosis, CRP was increased at 10.2 mg/dl. Blood, urine and peritoneal effluent cultures were collected and iv. ceftriaxone 2 g qd was administered. Three days later the fever had disappeared but CRP increased to 17.8 mg/dl and peritoneal fluid leukocytes rose to 600/mm3. On day 6 the peritoneal effluent culture grew Cryptococcus Neoformans. Intravenous liposomal Amphotericine B 200 mg/day and Flucytosine 2.5 g/day were administered for 4 weeks, with prompt clinical improvement. The PD catheter was removed, and hemodialysis was started. Cryptococcal peritonitis is uncommon, with only 15 cases described in peritoneal dialysis (PD) patients out of 61 reported between 1951 and 2012, but infection with the pathogen is a recognized complication of immunosuppression. Diagnosis is often difficult while prompt treatment is required. This potentially severe infection should be considered in any PD patients with clinical signs of culture negative peritonitis and recent or ongoing immunosuppressive therapy.
肾移植失败后发生capd相关隐球菌性腹膜炎1例
一位80岁的男性,患有严重动脉粥样硬化和缺血性肾病相关的慢性肾脏疾病,在肾移植6年后逐渐发展为糖尿病和尿毒症。免疫抑制包括雷帕霉素1 mg qd、霉酚酸500 mg qd、强的松2.5 mg qd。当CAPD开始时,仅维持低剂量强的松以保持剩余肾功能。进入CAPD第30天,患者出现发热(38.4℃):腹部压痛,PD导管出口部位健康,腹膜液清澈。胸部、腹部和脑部成像均为阴性。血(17.340/mm3)、腹膜液(190/mm3)白细胞增多,CRP升高10.2 mg/dl。收集血、尿和腹膜流出液培养,静脉注射头孢曲松2 g / d。3天后发烧消失,但CRP升高至17.8 mg/dl,腹膜液白细胞升高至600/mm3。第6天,腹膜流出物培养出新型隐球菌。两性霉素B脂质体200 mg/d、氟胞嘧啶2.5 g/d静脉注射4周,临床立即改善。取下PD导管,开始血液透析。隐球菌性腹膜炎并不常见,1951年至2012年间报道的61例腹膜透析(PD)患者中只有15例被描述为隐球菌性腹膜炎,但病原体感染是公认的免疫抑制并发症。诊断通常很困难,需要及时治疗。任何有培养阴性腹膜炎临床症状且近期或正在接受免疫抑制治疗的PD患者都应考虑这种潜在的严重感染。
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