Habib Sayed Meelad, Dor Frank Johan Marinus Frederik, Korte Mario Richard, Hagen Sander Martijn, Betjes Michiel Gerardus Henricus
Department of Internal Medicine, Division of Nephrology and Transplantation, Erasmus Medical Center, D-414, P,O, Box 2040, Rotterdam 3000, CA, The Netherlands.
BMC Nephrol. 2013 Sep 26;14:203. doi: 10.1186/1471-2369-14-203.
Post-transplantation encapsulating peritoneal sclerosis (EPS) causing bowel obstruction has been identified as a serious complication after kidney transplantation in patients previously treated with peritoneal dialysis. Systemic inflammation and abnormalities on an abdominal computed tomography (CT) scan are important hallmarks of EPS. To our knowledge, this is the first report of a case being diagnosed with late-onset post-transplantation EPS without systemic inflammation or abnormalities on a CT scan which could only be diagnosed by laparotomy.
A 59-year old female presented because of symptoms of bowel obstruction 33 months after kidney transplantation. The patient had a 26-month history of peritoneal dialysis before her first kidney transplantation and was treated with peritoneal dialysis for 4 years before undergoing a second kidney transplantation. Physical examination was unremarkable and laboratory tests showed no signs of systemic inflammation (C-reactive protein <1 mg/L). An abdominal CT scan did not reveal any abnormalities fitting the diagnosis of EPS, except a "feces sign". Given the severity of the progressive symptoms, a diagnostic laparotomy was performed, visualizing a classical EPS. Total peritonectomy and enterolysis were performed, leading to restoration of peristalsis.
EPS may occur several years after kidney transplantation in the absence of inflammation and typical radiological abnormalities. Obtaining a diagnosis of post-transplantation EPS is challenging, however, a low threshold for surgical exploration in case of high clinical suspicion and negative findings on the CT scan is mandatory.
移植后包裹性腹膜硬化症(EPS)导致肠梗阻已被确认为既往接受腹膜透析治疗的患者肾移植后的一种严重并发症。全身炎症反应和腹部计算机断层扫描(CT)异常是EPS的重要特征。据我们所知,这是首例在无全身炎症反应或CT扫描异常的情况下被诊断为迟发性移植后EPS的病例,该病例只能通过剖腹探查确诊。
一名59岁女性在肾移植33个月后因肠梗阻症状就诊。该患者在首次肾移植前有26个月的腹膜透析史,在接受第二次肾移植前接受了4年的腹膜透析治疗。体格检查无异常,实验室检查未显示全身炎症反应迹象(C反应蛋白<1mg/L)。腹部CT扫描未发现任何符合EPS诊断的异常,仅见“粪便征”。鉴于进行性症状的严重性,进行了诊断性剖腹探查,发现典型的EPS。行全腹膜切除术和肠粘连松解术,恢复了肠蠕动。
EPS可能在肾移植数年后发生,且无炎症反应和典型的影像学异常。然而,要获得移植后EPS的诊断具有挑战性,对于临床高度怀疑但CT扫描结果为阴性的病例,应保持较低的手术探查阈值。