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连续成年腹腔疾病患者的症状和血液学特征。

Symptoms and haematologic features in consecutive adult coeliac patients.

作者信息

Bodé S, Gudmand-Høyer E

机构信息

Dept. of Medical Gastroenterology, University of Copenhagen, Denmark.

出版信息

Scand J Gastroenterol. 1996 Jan;31(1):54-60. doi: 10.3109/00365529609031627.

Abstract

BACKGROUND

The aim of this study was to determine in a homogeneous adult population from Denmark, which is known to have very low incidence rates of coeliac disease, 1) the percentage of patients presenting with mild or atypical symptoms; 2) a possible change in clinical pattern over time; and 3) the delay in diagnosis and the age and sex distribution.

METHODS

The symptoms, delay in diagnosis, age, sex, and haematologic features of 50 consecutive adult coeliac patients, diagnosed by the same person in a uniform manner, are presented.

RESULTS

The median age was 40.5 (range, 17-82) years. The male to female sex ratio was 1:2.8. The median delay in diagnosis was 3 years. Fifty-eight per cent reported symptoms that could be attributed to coeliac disease during childhood. Presenting symptoms were tiredness, 78%; borborygmus, 72%; abdominal pain, 64%; diarrhoea, 56%; weight loss, 44%; vomiting, 16%; constipation, 12%; bone pain, 12%; and dermatitis herpetiformis, 10%. Weight gain after treatment was experienced by 84%. As a group the coeliac patients had many abnormal blood analysis results, but many patients had several test results inside the normal range. Only 22% had anemia. Liver involvement was not an uncommon feature (19% had increased transaminase levels). Low values were registered in s-iron (32%), p-folate (49%), c-folate (35%), p-vitamin B12 (11%), p-coagulation factors (II, VII, X) (32%), s-protein (21%), s-albumin (26%), s-calcium (43%), p-magnesium (13%), and s-zinc (31%). High/low IgG levels were 3%/8%; high, IgA 21%; high/low IgM, 65%/14%; and high IgE, 71%. The gliadin antibody test was the best screening test (81% positive). No changes in clinical pattern were demonstrated during the period.

CONCLUSION

The percentage of patients presenting with anaemia (22%) and other haematologic signs of malabsorption was one of the lowest reported ever. This emphasizes the highly variable and subtle clinical expression of adult coeliac disease.

摘要

背景

本研究旨在确定丹麦的同质成年人群中(已知该国乳糜泻发病率极低):1)出现轻度或非典型症状的患者百分比;2)临床模式随时间的可能变化;3)诊断延迟情况以及年龄和性别分布。

方法

呈现了由同一人以统一方式诊断的50例成年乳糜泻患者的症状、诊断延迟、年龄、性别和血液学特征。

结果

中位年龄为40.5岁(范围17 - 82岁)。男女比例为1:2.8。中位诊断延迟为3年。58%的患者报告在儿童期有可归因于乳糜泻的症状。出现的症状有疲倦(78%)、肠鸣音(72%)、腹痛(64%)、腹泻(56%)、体重减轻(44%)、呕吐(16%)、便秘(12%)、骨痛(12%)和疱疹样皮炎(10%)。84%的患者治疗后体重增加。作为一个群体,乳糜泻患者有许多异常血液分析结果,但许多患者有多项检测结果在正常范围内。只有22%的患者有贫血。肝脏受累并非罕见特征(19%的患者转氨酶水平升高)。血清铁(32%)、血浆叶酸(49%)、红细胞叶酸(35%)、血浆维生素B12(11%)、血浆凝血因子(II、VII、X)(32%)、血清蛋白(21%)、血清白蛋白(26%)、血清钙(43%)、血浆镁(13%)和血清锌(31%)值较低。高/低IgG水平为3%/8%;高IgA为21%;高/低IgM为65%/14%;高IgE为71%。麦醇溶蛋白抗体检测是最佳筛查试验(81%阳性)。在此期间未显示临床模式有变化。

结论

出现贫血(22%)和其他吸收不良血液学体征的患者百分比是有史以来报告的最低百分比之一。这强调了成人乳糜泻临床表型的高度变异性和隐匿性。

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