Lee In Hee, Kim Hong Ik, Kim Min-Kyung, Ahn Dong Jik
Department of Internal Medicine, Daegu Catholic University School of Medicine, Daegu, South Korea.
Department of Pathology, Dongguk University College of Medicine, Gyeongju, South Korea.
Am J Case Rep. 2021 Apr 13;22:e930677. doi: 10.12659/AJCR.930677.
BACKGROUND Pediatric patients with nephrotic syndrome have a high risk of developing spontaneous bacterial peritonitis (SBP). However, SBP in adults with nephrotic syndrome is very rare. We report a case of SBP induced by Escherichia coli in a 60-year-old male patient on immunosuppressive therapy for the treatment of minimal change disease (MCD). CASE REPORT The patient was hospitalized with abdominal pain and generalized edema that had lasted for 2 weeks. The patient first started treatment with high-dose oral prednisolone after being diagnosed with MCD 6 months ago. Complete remission of nephrotic syndrome was not achieved even after 5 months of treatment. Thus, the treatment was changed to combination therapy with cyclosporine and low-dose prednisolone. At the time of admission, leukocytosis, hypoalbuminemia, decreased serum immunoglobulin G (IgG), azotemia, and nephrotic-range proteinuria were observed. Ascitic fluid analysis showed a leukocyte count of 4960/μL (neutrophils 90%). On the suspicion of SBP associated with MCD, intravenous administration of empirical cefotaxime and supportive therapy were initiated; however, symptoms of peritonitis persisted. Extended-spectrum beta-lactamase-negative E. coli was found in ascites cultures. Laparoscopy-assisted peritoneal biopsy revealed no evidence of fungal infection; however, chronic inflammation without granuloma formation was noted. Afterward, cefotaxime was changed to piperacillin-tazobactam. After 4 weeks of antibacterial therapy, the peritonitis was cured and renal function was improved. CONCLUSIONS Adult patients with steroid-resistant MCD accompanied by refractory ascites, severe hypoalbuminemia, and marked reduction in serum IgG are at a high risk of subsequent SBP and require careful monitoring.
背景 小儿肾病综合征患者发生自发性细菌性腹膜炎(SBP)的风险很高。然而,成人肾病综合征患者发生SBP的情况非常罕见。我们报告一例60岁男性患者,因微小病变病(MCD)接受免疫抑制治疗,发生了由大肠杆菌引起的SBP。病例报告 患者因腹痛和全身水肿住院2周。该患者6个月前被诊断为MCD后开始使用大剂量口服泼尼松龙治疗。即使经过5个月的治疗,肾病综合征仍未完全缓解。因此,治疗改为环孢素与小剂量泼尼松龙联合治疗。入院时,观察到白细胞增多、低白蛋白血症、血清免疫球蛋白G(IgG)降低、氮质血症和肾病范围蛋白尿。腹水分析显示白细胞计数为4960/μL(中性粒细胞90%)。怀疑与MCD相关的SBP,开始静脉给予经验性头孢噻肟和支持治疗;然而,腹膜炎症状持续存在。腹水培养发现产超广谱β-内酰胺酶阴性的大肠杆菌。腹腔镜辅助腹膜活检未发现真菌感染的证据;然而,注意到有慢性炎症但无肉芽肿形成。此后,头孢噻肟改为哌拉西林-他唑巴坦。经过4周的抗菌治疗,腹膜炎治愈,肾功能改善。结论 伴有难治性腹水、严重低白蛋白血症和血清IgG明显降低的成人激素抵抗性MCD患者发生后续SBP的风险很高,需要仔细监测。