Simonetto Douglas A, Fatima Hala, Zijlstra Folkert, Zijlstra Michael K
Department of Gastroenterology, Mayo Clinic Rochester, Rochester, Minnesota, USA.
Department of Gastroenterology-Hepatology, Indiana University Health University Hospital, Indianapolis, Indiana, USA.
Case Rep Gastroenterol. 2018 May 31;12(2):207-216. doi: 10.1159/000488975. eCollection 2018 May-Aug.
Ascites is an abnormal accumulation of fluid within the peritoneal cavity. The most common cause of ascites in the United States population is portal hypertension secondary to cirrhosis, accounting for about 80% of the cases. Other etiologies include malignancy, heart failure, tuberculosis, and pancreatic disease. After an extensive literature review, it is to our best knowledge that there have been no cases reported on autoimmune ascites. We present an interesting case of ascites in a 67-year-old Caucasian male with symptoms of recurrent abdominal distention and significant weight gain, refractory to standard therapies. An extensive 3-year long workup was only significant for serum-ascites albumin gradient > 1.1 g/dL, ascitic fluid protein of 3.0 g/dL, and peritoneal biopsies showing minor inflammatory changes. Both common and rare causes of ascites were ruled out. Empiric treatment with mycophenolate mofetil (CellCept) resulted in resolution of symptoms with no need for a repeat paracentesis for > 2 years, suggesting the diagnosis of autoimmune ascites.
腹水是腹腔内液体的异常积聚。在美国人群中,腹水最常见的原因是肝硬化继发门静脉高压,约占病例的80%。其他病因包括恶性肿瘤、心力衰竭、结核病和胰腺疾病。经过广泛的文献检索,据我们所知,尚无自身免疫性腹水的病例报道。我们报告了一例有趣的腹水病例,患者为67岁的白种男性,有反复腹胀和体重显著增加的症状,对标准治疗无效。长达3年的全面检查仅发现血清腹水白蛋白梯度>1.1g/dL、腹水蛋白为3.0g/dL以及腹膜活检显示轻微炎症变化。常见和罕见的腹水病因均被排除。用霉酚酸酯(骁悉)进行经验性治疗使症状得到缓解,超过2年无需重复腹腔穿刺术,提示为自身免疫性腹水。