Dhandhu Bhanwar Singh, Gupta Gaurav Kumar, Wanjari Shashank J, Sharma Nidhi, Nijhawan Sandeep
Department of Gastroenterology, Sawai Man Singh Medical College, J L N Marg, Jaipur, 302 004, India.
Department of Pathology, Sawai Man Singh Medical College, J L N Marg, Jaipur, 302 004, India.
Indian J Gastroenterol. 2018 Mar;37(2):98-102. doi: 10.1007/s12664-018-0821-5. Epub 2018 Feb 13.
Celiac disease (CeD) requires a biopsy from the small intestine to confirm the diagnosis. Conventionally, duodenal bulb (D1) was avoided as a biopsy site due to histological confounding factors at this site. However, sometimes, the bulb mucosa is the only affected site. The aim of the present study was to assess changes in duodenal bulb histology and compare it to distal duodenal histology and to analyze whether the addition of duodenal bulb biopsy increases the diagnostic yield of the CeD.
It was a prospective study comprising of 98 patients of CeD who were symptomatic clinically and had positive anti tissue transglutaminase (tTG) antibody. Endoscopically four mucosal biopsies were taken, two each from the bulb and distal duodenum, and morphology was graded as per modified Marsh grade.
Iron deficiency anemia (40%) was a most common clinical presentation followed by chronic diarrhea (30%). Sixty patients showed same Marsh grade and 38 showed different Marsh grade at both sites. Patients who were showing the difference in the Marsh grade at the two biopsy sites, in place of; descending duodenum showed higher grade in 24 patients while higher mucosal atrophy was documented in the bulb in 14 patients. No patient of CeD had isolated D1 involvement. In eight patients, the correct diagnosis of CeD could be made only because of bulb biopsy.
Majority of the patients had no classical symptoms. Different Marsh grade at the two biopsy sites was documented demonstrating the patchy distribution of CeD. Combining biopsy from both bulb and descending duodenum maximizes the diagnostic yield of the CeD.
乳糜泻(CeD)需要通过小肠活检来确诊。传统上,由于十二指肠球部(D1)存在组织学混杂因素,该部位不作为活检部位。然而,有时球部黏膜是唯一受影响的部位。本研究的目的是评估十二指肠球部组织学的变化,并将其与十二指肠远端组织学进行比较,分析增加十二指肠球部活检是否能提高CeD的诊断率。
这是一项前瞻性研究,纳入了98例临床有症状且抗组织转谷氨酰胺酶(tTG)抗体阳性的CeD患者。在内镜下取4块黏膜活检组织,球部和十二指肠远端各取2块,并根据改良的Marsh分级对形态进行分级。
缺铁性贫血(40%)是最常见的临床表现,其次是慢性腹泻(30%)。60例患者在两个部位的Marsh分级相同,38例患者在两个部位的Marsh分级不同。在两个活检部位Marsh分级存在差异的患者中,十二指肠降部有24例显示较高分级,而球部有14例记录到更高的黏膜萎缩。没有CeD患者仅表现为孤立的D1受累。在8例患者中,仅通过球部活检才能做出CeD的正确诊断。
大多数患者没有典型症状。记录到两个活检部位的Marsh分级不同,表明CeD呈斑片状分布。联合球部和十二指肠降部活检可使CeD的诊断率最大化。