Morreale Gaetano Cristian, Montalbano Luigi Maria, Cappello Maria, Sinagra Emanuele, Rizzo Aroldo, Carroccio Antonio
Gastroenterology and Hepatology Section, DIBIMIS, University of Palermo, Italy.
Endoscopic Unit, Ospedali Riuniti Villa Sofia-Cervello Palermo, Italy.
Arab J Gastroenterol. 2017 Dec;18(4):241-244. doi: 10.1016/j.ajg.2017.09.011. Epub 2018 Jan 8.
Villous atrophy in absence of coeliac disease (CD)-specific antibodies represents a diagnostic dilemma. We report a case of a woman with anaemia, weight loss and diarrhoea with an initial diagnosis of seronegative CD and a histological documented villous atrophy who did not improve on gluten-free diet due to the concomitant presence of common variable immunodeficiency (CVID) and Giardia lamblia infection. This case report confirms that CD diagnosis in CVID patients is difficult; the combination of anti-endomysial antibodies (EmA-IgA), anti-tissue transglutaminase antibodies (tTG-IgAb) antibodies and total IgA is obligatory in basic diagnostic of CD but in CVID are negative. Furthermore, the typical histological aspects of the intestinal mucosa in CVID (absence of plasma cells and switch to the IgD immunoglobulins), cannot rule out a concomitant CD diagnosis. HLA typing in this setting has a low positive predictive value but should be considered. Histological response to a gluten-free diet on repeat biopsy and the concomitant treatment of other causes of villous atrophy leads to a definite diagnosis of CD.
无乳糜泻(CD)特异性抗体情况下的绒毛萎缩是一个诊断难题。我们报告一例患有贫血、体重减轻和腹泻的女性病例,最初诊断为血清阴性CD,组织学证实有绒毛萎缩,但由于同时存在普通可变免疫缺陷(CVID)和蓝氏贾第鞭毛虫感染,无麸质饮食治疗后病情未改善。本病例报告证实,CVID患者的CD诊断困难;抗肌内膜抗体(EmA-IgA)、抗组织转谷氨酰胺酶抗体(tTG-IgAb)和总IgA联合检测在CD的基本诊断中是必需的,但在CVID患者中呈阴性。此外,CVID患者肠道黏膜的典型组织学表现(浆细胞缺失和向IgD免疫球蛋白转换)不能排除同时存在CD的诊断。在这种情况下,HLA分型的阳性预测值较低,但仍应予以考虑。重复活检时对无麸质饮食的组织学反应以及对其他绒毛萎缩原因的同时治疗有助于明确CD诊断。