Smyrk Thomas C
Department of Pathology, Mayo Clinic, Hilton 11, 200 First Street Southwest, Rochester, MN 55902, USA.
Surg Pathol Clin. 2017 Dec;10(4):823-839. doi: 10.1016/j.path.2017.07.004. Epub 2017 Sep 23.
Celiac disease features duodenal intraepithelial lymphocytosis with or without villous atrophy. Lymphocytosis without villous atrophy will be proven to represent celiac disease in 10% to 20% of cases. The differential diagnosis is broad: Helicobacter pylori gastritis, NSAID injury and bacterial overgrowth are considerations. Lymphocytosis with villous atrophy is very likely to be celiac disease, but there are mimics to consider, including collagenous sprue, tropical sprue, drug injury, and common variable immunodeficiency. Histologic clues to a diagnosis other than celiac disease include paucity of plasma cells, excess of neutrophils, granulomas, and relative paucity of intraepithelial lymphocytes.
乳糜泻的特征为十二指肠上皮内淋巴细胞增多,可伴有或不伴有绒毛萎缩。在10%至20%的病例中,无绒毛萎缩的淋巴细胞增多将被证实为乳糜泻。鉴别诊断范围广泛:需考虑幽门螺杆菌胃炎、非甾体抗炎药损伤和细菌过度生长。伴有绒毛萎缩的淋巴细胞增多很可能是乳糜泻,但也有一些类似情况需要考虑,包括胶原性口炎性腹泻、热带口炎性腹泻、药物损伤和常见变异型免疫缺陷。除乳糜泻外,其他诊断的组织学线索包括浆细胞缺乏、中性粒细胞增多、肉芽肿以及上皮内淋巴细胞相对缺乏。