Lynch D A, Sobala G M, Dixon M F, Gledhill A, Jackson P, Crabtree J E, Axon A T
Centre for Digestive Diseases, General Infirmary at Leeds.
J Clin Pathol. 1995 Oct;48(10):939-45. doi: 10.1136/jcp.48.10.939.
To investigate the natural history of lymphocytic gastritis (LG) and its relation to Helicobacter pylori infection and to coeliac disease using serology, duodenal biopsy and a small intestinal permeability test.
Twenty two patients diagnosed as having LG between 1984 and 1994 were investigated by upper gastrointestinal endoscopy at which gastric and duodenal biopsy specimens were taken for histological assessment and immunohistology. Serum was collected for measurement of anti-H pylori, anti-gliadin and anti-endomysial antibodies. A lactulose/mannitol absorption test was performed within one week of endoscopy. Control groups were studied by histology, serology and permeability tests.
Three patients had been recently diagnosed as having LG while 15 still had the condition after a mean of 13.9 (range two to 38) months. LG involved the antrum alone in three patients, antrum and body in seven, body alone in six, and gastric remnant in two. Gastroduodenal intraepithelial lymphocytes (IELs) were T cells and predominantly of T suppressor (CD8) type. Duodenal IELs were increased compared to age/sex matched controls with chronic gastritis. Four patients had duodenal villous atrophy. Four patients no longer had LG after a mean of 29.3 (10-70) months but had increased gastroduodenal IELs. H pylori was present in four (22%) of 18 patients with LG but H pylori serology was positive in 11 (61%) of 18. There was no difference in seropositivity when compared with age/sex matched controls with dyspepsia. Eleven of 20 patients with LG tested had abnormal lactulose/mannitol absorption (v none of 22 controls with chronic gastritis). Four patients with LG, all with villous atrophy, were seropositive for IgA endomysial antibody.
The persistence of LG with time, the association with increased duodenal IELs and abnormal small intestinal permeability suggests LG may be a manifestation of a diffuse lymphocytic gastroenteropathy related to sensitivity to gluten or some other agent.
采用血清学、十二指肠活检及小肠通透性试验,研究淋巴细胞性胃炎(LG)的自然病程及其与幽门螺杆菌感染和乳糜泻的关系。
对1984年至1994年间诊断为LG的22例患者进行上消化道内镜检查,取胃和十二指肠活检标本进行组织学评估和免疫组织学检查。采集血清检测抗幽门螺杆菌、抗麦醇溶蛋白和抗肌内膜抗体。在内镜检查后一周内进行乳果糖/甘露醇吸收试验。通过组织学、血清学和通透性试验对对照组进行研究。
3例患者近期诊断为LG,15例患者在平均13.9(2至38)个月后仍患有该病。LG仅累及胃窦3例,胃窦和胃体7例,仅胃体6例,胃残端2例。胃十二指肠上皮内淋巴细胞(IEL)为T细胞,主要是抑制性T细胞(CD8)类型。与年龄/性别匹配的慢性胃炎对照组相比,十二指肠IEL增加。4例患者有十二指肠绒毛萎缩。4例患者在平均29.3(10至70)个月后不再患有LG,但胃十二指肠IEL增加。18例LG患者中有4例(22%)存在幽门螺杆菌,但18例中有11例(61%)幽门螺杆菌血清学呈阳性。与年龄/性别匹配的消化不良对照组相比,血清阳性率无差异。20例接受检测的LG患者中有11例乳果糖/甘露醇吸收异常(22例慢性胃炎对照组均无异常)。4例LG患者均有绒毛萎缩,IgA肌内膜抗体血清学呈阳性。
LG随时间持续存在,与十二指肠IEL增加和小肠通透性异常相关,提示LG可能是与麸质或其他某种物质敏感性相关的弥漫性淋巴细胞性胃肠病的一种表现。