Malignant complications of coeliac disease.
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Summary
Loss of response to a gluten free diet (refractory coeliac disease) and ulcerative jejunitis are two recently described complications of CD that may progress to an Enteropathy-Associated T-cell Lymphoma (EATL), which most often appears at extra-nodal sites, essentially the small bowel.
- Type
- article
- Published
- 2005-06-01
- Cited by
- 126
- References
- 49
- OpenAlex
- https://openalex.org/W15925845
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:7964751
Keywords
Geography
References
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Cited by
- Enteropathy associated T-cell lymphoma presenting with multiple episodes of small bowel haemorrhage and perforation
- Atypical presentations of celiac disease.
- Celiac disease and postcricoid carcinoma.
- Gluten enteropatisinin nadir ve cerrahi ile tanı konan komplikasyonu: Enteropati ilişkili T-hücreli lenfoma
- DOENÇA CELÍACA REVISITADA
- Alteraciones genéticas, inestabilidad genómica y cáncer en enfermedad celíaca
- Celiac disease in children
- On diagnostic tools in coeliac disease and its complicated forms
- Immunochemical analysis of prolamins in gluten-free foods
- The imaging of coeliac disease and its complications.
- Hepatic Hemangioma in Celiac Patients: Data from a Large Consecutive Series
- World Gastroenterology Organisation Global Guidelines: probiotics and prebiotics October 2011.
- A case of sequential development of celiac disease and ulcerative colitis
- Small bowel adenocarcinoma in a patient with Coeliac disease: A case report
- Chromosome Instability in Lymphocytes of Children With Coeliac Disease
- Hematologic manifestations of celiac disease.
- Effect of a Gluten-free Diet on the Risk of Enteropathy-associated T-cell Lymphoma in Celiac Disease
- The Production of the Oral Mucosa of Antiendomysial and Anti—Tissue-Transglutaminase Antibodies in Patients with Celiac Disease: A Review
- Adult Celiac Disease and Its Malignant Complications
- Analysis of genomic instability in adult-onset celiac disease patients by microsatellite instability and loss of heterozygosis
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