Querido Sara, Sousa Henrique Silva, Pereira Tiago Assis, Birne Rita, Matias Patrícia, Jorge Cristina, Weigert André, Adragão Teresa, Bruges Margarida, Machado Domingos
Department of Nephrology, Centro Hospitalar do Médio Tejo, Avenida Xanana Gusmão, Apartado 45, 2350-754 Torres Novas, Portugal.
Department of Nephrology, Centro Hospitalar de Lisboa Ocidental, Avenida Professor Reinaldo dos Santos, 2790-134 Carnaxide, Portugal.
Case Rep Transplant. 2015;2015:424508. doi: 10.1155/2015/424508. Epub 2015 Dec 10.
A 56-year-old African patient received a kidney from a deceased donor with 4 HLA mismatches in April 2013. He received immunosuppression with basiliximab, tacrolimus, mycophenolate mofetil, and prednisone. Immediate diuresis and a good allograft function were soon observed. Six months later, the serum creatinine level increased to 2.6 mg/dL. A renal allograft biopsy revealed interstitial fibrosis and tubular atrophy grade II. Toxicity of calcineurin inhibitor was assumed and, after a switch for everolimus, renal function improved. However, since March 2014, renal function progressively deteriorated. A second allograft biopsy showed no new lesions. Two months later, the patient was admitted due to anuria, haematochezia with anaemia, requiring 5 units of packed red blood cells, and diffuse skin thickening. Colonoscopy showed haemorrhagic patches in the colon and the rectum; histology diagnosis was Kaposi sarcoma (KS). A skin biopsy revealed cutaneous involvement of KS. Rapid clinical deterioration culminated in death in June 2014. This case is unusual as less than 20 cases of KS with gross gastrointestinal bleeding have been reported and only 6 cases had the referred bleeding originating in the lower gastrointestinal tract. So, KS should be considered in differential diagnosis of gastrointestinal bleeding in some kidney transplant patients.
一名56岁的非洲患者于2013年4月接受了来自一名已故供体的肾脏,该供体与患者有4个HLA错配。他接受了巴利昔单抗、他克莫司、霉酚酸酯和泼尼松的免疫抑制治疗。很快观察到立即利尿且移植肾功能良好。6个月后,血清肌酐水平升至2.6mg/dL。移植肾活检显示间质纤维化和肾小管萎缩为II级。考虑是钙调神经磷酸酶抑制剂的毒性作用,改用依维莫司后,肾功能有所改善。然而,自2014年3月起,肾功能逐渐恶化。第二次移植肾活检未发现新病变。两个月后,患者因无尿、便血伴贫血入院,需要输注5单位浓缩红细胞,且皮肤弥漫性增厚。结肠镜检查显示结肠和直肠有出血斑;组织学诊断为卡波西肉瘤(KS)。皮肤活检显示KS累及皮肤。临床迅速恶化,最终于2014年6月死亡。该病例不同寻常,因为据报道,胃肠道大出血的KS病例不到20例,只有6例出血源自下消化道。因此,对于一些肾移植患者胃肠道出血的鉴别诊断,应考虑KS。