Nagashima Takao, Yabe Hiroki, Okabe Naota, Kobashigawa Tsuyoshi
Division of Rheumatology, First Department of Comprehensive Medicine, Jichi Medical University Saitama Medical Center, Japan.
Department of Pathology, Jichi Medical University Saitama Medical Center, Japan.
Intern Med. 2025 Mar 1;64(5):699-704. doi: 10.2169/internalmedicine.3769-24. Epub 2024 Aug 1.
A 76-year-old woman with persistent diarrhea was referred to our hospital. She had purpura, peripheral eosinophilia (18,177/μL), and an elevated serum IgG4 level (819 mg/dL). Abdominal computed tomography revealed massive ascites and bowel edema. A skin biopsy of the purpura revealed leukocytoclastic vasculitis with prominent eosinophilic infiltration. Biopsies of the gastrointestinal mucosa revealed dense eosinophilic infiltration, indicating eosinophilic gastroenteritis (EG) associated with the hypereosinophilic syndrome. The number of IgG4-positive cells increased in the duodenal mucosa; however, the diagnostic criteria for IgG4-related disease (IgG4-RD) were not met. Whether or not EG with ascites is a manifestation of IgG4-RD warrants further investigation.
一名76岁持续性腹泻的女性被转诊至我院。她有紫癜、外周血嗜酸性粒细胞增多(18,177/μL)以及血清IgG4水平升高(819 mg/dL)。腹部计算机断层扫描显示大量腹水和肠水肿。紫癜的皮肤活检显示白细胞破碎性血管炎伴显著嗜酸性粒细胞浸润。胃肠道黏膜活检显示密集嗜酸性粒细胞浸润,提示与高嗜酸性粒细胞综合征相关的嗜酸性粒细胞性胃肠炎(EG)。十二指肠黏膜中IgG4阳性细胞数量增加;然而,未满足IgG4相关疾病(IgG4-RD)的诊断标准。伴有腹水的EG是否为IgG4-RD的一种表现值得进一步研究。