Nanjo Sohachi, Nishikawa Jun, Miwa Shigeharu, Mihara Hiroshi, Fujinami Haruka, Yoshita Hiroki, Ueda Akira, Kajiura Shinya, Hasumoto Yushi, Ando Takayuki, Hosokawa Ayumu, Sugiyama Toshiro
Department of Gastroenterology and Hematology, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, Japan.
Intern Med. 2014;53(20):2301-5. doi: 10.2169/internalmedicine.53.1980. Epub 2014 Oct 15.
A 28-year-old woman previously diagnosed to have Down syndrome presented with a one-month history of severe hypoalbuminemia, lower extremity edema, and diarrhea. Her urine was negative for protein. She was diagnosed with immune-mediated protein-losing enteropathy (PLE) based on clinical findings, protein loss evident on (99m)Technetium-labeled human serum albumin scintigraphy, and IgM and complement C3 deposition in the duodenum. She did not exhibit any manifestations of collagen diseases. A dramatic remission was achieved and maintained with corticosteroid administration. This is the first report of immune-mediated PLE in a patient with Down syndrome.
一名先前被诊断患有唐氏综合征的28岁女性,出现了严重低白蛋白血症、下肢水肿和腹泻1个月的病史。她的尿液蛋白呈阴性。根据临床表现、锝标记人血清白蛋白闪烁扫描显示的蛋白丢失以及十二指肠中IgM和补体C3沉积,她被诊断为免疫介导的蛋白丢失性肠病(PLE)。她没有表现出任何胶原病的症状。通过给予皮质类固醇实现并维持了显著缓解。这是唐氏综合征患者免疫介导的PLE的首例报告。