Celiac Disease Center, Columbia University College of Physicians and Surgeons, Columbia University Medical Center, New York, NY 10032, USA.
Am J Gastroenterol. 2013 May;108(5):647-53. doi: 10.1038/ajg.2013.45.
Patients with villous atrophy (VA) and negative celiac disease (CD) serologies pose a diagnostic and therapeutic dilemma. When a definitive etiology for VA is not determined, patients are characterized as having unclassified sprue (US), the optimal management of which is unknown.
We studied adult patients with VA on biopsy and negative celiac serologies, evaluated at our tertiary referral center over a 10-year period. Testing for HLA DQ2/8 alleles, antienterocyte antibodies, giardia stool antigen, bacterial overgrowth, total serum immunoglobulins, and HIV was noted. Treatment, response, and repeat-biopsy findings were recorded.
The most common diagnoses of the 72 patients were seronegative CD, medication-related villous atrophy, and US. Of those with US, the majority reported symptomatic improvement with immunosuppressive therapy. Some patients initially labeled as unclassified were found to have VA associated with olmesartan use.
The role of medications in the development of VA and the optimal dose and length of immunosuppression for patients with US should be investigated further.
绒毛萎缩(VA)和阴性乳糜泻(CD)血清学患者构成了诊断和治疗的难题。当无法确定 VA 的明确病因时,患者被归类为未分类的脂肪泻(US),其最佳治疗方法尚不清楚。
我们研究了在我们的三级转诊中心进行的为期 10 年的活检和阴性乳糜泻血清学检查的成年 VA 患者。注意检测 HLA DQ2/8 等位基因、抗肠细胞抗体、贾第虫粪便抗原、细菌过度生长、总血清免疫球蛋白和 HIV。记录治疗、反应和重复活检结果。
72 名患者中最常见的诊断是血清阴性 CD、药物相关的绒毛萎缩和 US。在 US 中,大多数患者报告说免疫抑制治疗后症状有所改善。一些最初被归类为未分类的患者被发现与奥美沙坦的使用有关。
应进一步研究药物在 VA 发展中的作用以及 US 患者免疫抑制治疗的最佳剂量和时间。