Ritaccio Gabrielle, Asif Bilal, Yfantis Harris, Wong Uni
Department of Medicine, University of Maryland Medical Center, Baltimore, MD.
Digestive Diseases Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD.
ACG Case Rep J. 2021 Nov 24;8(11):e00659. doi: 10.14309/crj.0000000000000659. eCollection 2021 Nov.
Tangier disease is a rare autosomal recessive disease resulting in cholesterol deposition in different organs. We report a case of a 52-year-old white man who presented for chronic diarrhea without significant findings on noninvasive testing. Subsequent colonoscopy revealed endoscopically normal mucosa, with random biopsies remarkable for foamy macrophages in the lamina propria. Genetic testing showed adenosine triphosphate-binding cassette transporter gene mutation with low high-density lipoprotein and low low-density lipoprotein. To the best of our knowledge, this is the first report of chronic diarrhea in a patient with Tangier disease without any other clear etiology.
丹吉尔病是一种罕见的常染色体隐性疾病,会导致胆固醇在不同器官中沉积。我们报告了一例52岁白人男性病例,该患者因慢性腹泻就诊,无创检查未发现明显异常。随后的结肠镜检查显示内镜下黏膜正常,随机活检显示固有层有泡沫状巨噬细胞,这一点很显著。基因检测显示三磷酸腺苷结合盒转运体基因突变,伴有高密度脂蛋白降低和低密度脂蛋白降低。据我们所知,这是首例无其他明确病因的丹吉尔病患者出现慢性腹泻的报告。