Osaki Yosuke, Maeoka Yujiro, Sami Mai, Takahashi Akira, Ishiuchi Naoki, Sasaki Kensuke, Masaki Takao
Department of Nephrology, Hiroshima University Hospital, 1-2-3 Kasumi, Minami-Ku, Hiroshima, 734-8551, Japan.
CEN Case Rep. 2025 Feb;14(1):1-5. doi: 10.1007/s13730-024-00894-y. Epub 2024 Jun 2.
Peritoneal dialysis (PD)-associated peritonitis is a common complication of PD. Enteric peritonitis is defined as peritonitis arising from an intestinal or intra-abdominal organ source. The delay in the diagnosis or treatment of enteric peritonitis has been reported to increase mortality. Therefore, the early consideration of enteric peritonitis, particularly in cases of culture-negative peritonitis, is imperative. A 67-year-old Japanese man who had been undergoing PD for 3 years, was admitted to our hospital with a diagnosis of PD-associated peritonitis. A month previously, he experienced a bleeding gastric ulcer, which led to severe anemia (hemoglobin 6.3 mg/dL), followed by thrombocytosis. On admission, peritoneal fluid analysis showed a high white blood cell count (WBC: 8,570 /µL), with neutrophils predominating (74.5%). Cultures of both his dialysis effluent and blood were negative. After admission, the WBC count of the dialysis effluent gradually decreased alongside antibiotic therapy, but the patient's abdominal pain did not improve. After 4 days, enhanced computed tomography showed superior mesenteric artery (SMA) thrombosis and intestinal necrosis. Therefore, emergency intestinal resection and PD catheter removal were performed, and then antithrombosis therapy was initiated. Because the patient's abdominal pain was improved and platelet count and D-dimer concentration were reduced by these treatments, he was discharged from the hospital after 47 days. Thus, we report a rare case of culture-negative PD-associated peritonitis, which was caused by SMA thrombosis and intestinal necrosis. It is likely that combination of severe calcification of SMA and prolonged thrombocytosis secondary to the severe anemia contributed to the thrombosis.
腹膜透析(PD)相关腹膜炎是PD常见的并发症。肠源性腹膜炎定义为源于肠道或腹腔内器官的腹膜炎。据报道,肠源性腹膜炎诊断或治疗的延迟会增加死亡率。因此,必须尽早考虑肠源性腹膜炎,尤其是在培养阴性腹膜炎的病例中。一名67岁的日本男性,已接受PD治疗3年,因诊断为PD相关腹膜炎入住我院。一个月前,他患了出血性胃溃疡,导致严重贫血(血红蛋白6.3mg/dL),随后出现血小板增多症。入院时,腹膜液分析显示白细胞计数高(白细胞:8570/µL),以中性粒细胞为主(74.5%)。他的透析流出液和血液培养均为阴性。入院后,随着抗生素治疗,透析流出液的白细胞计数逐渐下降,但患者的腹痛并未改善。4天后,增强计算机断层扫描显示肠系膜上动脉(SMA)血栓形成和肠坏死。因此,进行了急诊肠切除术和PD导管拔除术,然后开始抗血栓治疗。由于这些治疗使患者的腹痛得到改善,血小板计数和D-二聚体浓度降低,他在47天后出院。因此,我们报告了一例罕见的培养阴性的PD相关腹膜炎病例,其由SMA血栓形成和肠坏死引起。SMA严重钙化和严重贫血继发的长期血小板增多症可能共同导致了血栓形成。