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JCR 2016
جستجوی مقالات
دوشنبه 24 آذر 1404
Middle East Journal of Digestive Diseases
، جلد ۱۴، شماره ۳، صفحات ۳۵۴-۳۵۸
عنوان فارسی
چکیده فارسی مقاله
کلیدواژههای فارسی مقاله
عنوان انگلیسی
Spontaneous Latency in Adult Patients with Celiac Disease on a Normal Diet after Gluten-Free Diet: Case Series
چکیده انگلیسی مقاله
Celiac disease (CeD) is an immune condition induced by the consumption of gluten-containing foods in genetically-predisposed persons. CeD, in addition to digestive disease, is a multisystem disorder. If untreated, it is potentially can be a dangerous disorder and lead to morbidity and even mortality. At present, the only treatment option is a lifelong Gluten-Free diet (GFD), and all authors recommended this regimen. To the best of our knowledge, there are rare reports of the complete remission of disorder on GFD and reintroduction of a normal diet in affected patients. In this report, we describe five patients with CeD who developed complete remission of clinical symptoms, histopathological changes, and serology on a gluten-containing diet. All patients had CeD based on a positive tissue transglutaminase antibody (TTG IgA) and typical histopathological changes in duodenal biopsy with the complete disappearance of symptoms on the GFD regimen. All patients followed GFD for a mean 4 (± 0.54) years. In conclusion, this study has shown that some CeD patients diagnosed in adulthood can recover a normal mucosa after a long period of the gluten-containing diet without relapsing any clinical or biological symptoms of CeD.
کلیدواژههای انگلیسی مقاله
Celiac disease,,Gluten, Remission,,Spontaneous latency
نویسندگان مقاله
| Alireza Bakhshipour
MD, MPH, Ph.D., Assistant professor, Department of Neuroscience, School of Advanced Technologies in Medicine, Mazandaran University of Medical Sciences, Sari, Iran.
| Raheleh Rafaiee
نشانی اینترنتی
http://mejdd.org/index.php/mejdd/article/view/2606
فایل مقاله
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کد مقاله (doi)
10.15171/middle east j di.v14i3.2606
زبان مقاله منتشر شده
en
موضوعات مقاله منتشر شده
نوع مقاله منتشر شده
Case Report
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