Chhoda Ankit, Jain Deepanshu, Kumar Daga Mradul, Batra Vineeta
Yale-Waterbury Internal Medicine Program, Yale University School of Medicine, Waterbury, CT.
Department of Gastroenterology and Hepatology, Albert Einstein Healthcare Network, Philadelphia, PA.
ACG Case Rep J. 2018 Mar 28;5:e24. doi: 10.14309/crj.2018.24. eCollection 2018.
We report a rare case of secondary renal amyloidosis in a patient with probable celiac disease presenting as nephrotic syndrome. A 30-year-old man with chronic diarrhea presented with progressive anasarca for 2 years. On further evaluation, he had hypoalbuminemia, significant nephrotic-range proteinuria, and elevated levels of anti-tissue transglutaminase. Renal biopsy suggested deposition of amorphous Congo red-positive material in the glomerular mesangium, positive for amyloid A amyloidosis. Endoscopic duodenal biopsy suggested blunting of the villous architecture and chronic inflammation of the lamina propria. The patient subsequently developed massive pulmonary embolism and died due to refractory cardiogenic shock.
我们报告了一例罕见的继发性肾淀粉样变性病例,患者可能患有乳糜泻,表现为肾病综合征。一名30岁慢性腹泻男性,出现进行性全身性水肿2年。进一步评估发现,他有低白蛋白血症、显著的肾病范围蛋白尿以及抗组织转谷氨酰胺酶水平升高。肾活检提示在肾小球系膜中有无定形刚果红阳性物质沉积,确诊为淀粉样A蛋白淀粉样变性。内镜下十二指肠活检提示绒毛结构变钝和固有层慢性炎症。该患者随后发生大面积肺栓塞,最终因难治性心源性休克死亡。