scholarly journals Esophagitis in Children with Celiac Disease

2011 ◽  
Vol 2011 ◽  
pp. 1-3 ◽  
Author(s):  
Wael N. Sayej ◽  
Razan AlKhouri ◽  
Robert D. Baker ◽  
Raza Patel ◽  
Susan S. Baker

Objectives. To our knowledge, the occurrence of esophagitis in children with celiac disease (CD) has never been evaluated. The aim of this study is to determine the prevalence of esophagitis in children with CD. Patients and Methods. Between 2003 and 2007, children with biopsy confirmed CD were retrospectively identified. Biopsy reports were reviewed for esophageal inflammation. Biopsy reports of 2218 endoscopies performed during the same period were also evaluated for inflammation. Results. Forty-nine children diagnosed with CD (47% boys). Nineteen of 49 (39%) patients with CD had esophagitis (95% CI 0.23–0.5). Thirty percent of boys and 46% of girls with CD had esophagitis (95% CI 0.12–0.40). Overall, 45% of patients who underwent upper endoscopy had esophagitis. The prevalence of esophagitis in CD (39%) compared to the prevalence of esophagitis (45%) in our practice was not significantly different, . Conclusion. There was no difference in the prevalence of esophagitis between children diagnosed with CD at the time of their diagnostic EGD and the prevalence of esophagitis in children without CD. A prospective study to determine whether the esophagitis should be treated with acid suppression or whether the esophagitis heals with the gluten-free diet is warranted.

2007 ◽  
Vol 102 ◽  
pp. S200
Author(s):  
Daniel A. Leffler ◽  
Jessica B. Edwards-George ◽  
Melinda Dennis ◽  
Detlef Schuppan ◽  
Ciaran P. Kelly

2010 ◽  
Vol 138 (5) ◽  
pp. S-308
Author(s):  
Fabio D. Nachman ◽  
Horacio Vázquez ◽  
Andrea F. Gonzalez ◽  
Paola J. Andrenacci ◽  
Sonia Niveloni ◽  
...  

2007 ◽  
Vol 102 ◽  
pp. S199-S200
Author(s):  
Daniel A. Leffler ◽  
Jessica B. Edwards George ◽  
Melinda D. Dennis ◽  
Hani Abdullah ◽  
Ciaran P. Kelly

2014 ◽  
Vol 61 (3) ◽  
pp. 558-563 ◽  
Author(s):  
Jamile′ Wakim-Fleming ◽  
Mangesh R. Pagadala ◽  
Arthur J. McCullough ◽  
Rocio Lopez ◽  
Ana E. Bennett ◽  
...  

2020 ◽  
Vol 07 (04) ◽  
pp. 140-143
Author(s):  
Surat Nabum ◽  
Hema Gupta Mittal ◽  
Vivek Dewan ◽  
Namrita Sachdev ◽  
Rahul Tiotia ◽  
...  

Endoscopy ◽  
2006 ◽  
Vol 38 (7) ◽  
pp. 702-707 ◽  
Author(s):  
A. Tursi ◽  
G. Brandimarte ◽  
G. Giorgetti ◽  
W. Elisei ◽  
C. Inchingolo ◽  
...  

1965 ◽  
Vol 48 (2) ◽  
pp. 155-172 ◽  
Author(s):  
I. Michael Samloff ◽  
John S. Davis ◽  
Eric A. Schenk

2016 ◽  
Vol 25 (4) ◽  
pp. 555-558
Author(s):  
Alina Popp

Background: Alveolar hemorrhage is a potentially life-threatening condition which is usually managed by the pulmonologist. When considering its etiology, there is a rare association that sets the disease into the hands of the gastroenterologist. Case presentation: We report the case of a 48 year-old female who was admitted to the intensive care unit for severe anemia and hemoptysis. On imaging, diffuse pulmonary infiltrates suggestive of alveolar hemorrhage were detected and a diagnosis of pulmonary hemosiderosis was made. She received cortisone therapy and hematologic correction of anemia, with slow recovery. In search of an etiology for the pulmonary hemosiderosis, an extensive workup was done, and celiac disease specific serology was found positive. After confirmation of celiac disease by biopsy, a diagnosis of Lane-Hamilton syndrome was established. The patient was recommended a gluten-free diet and at 6 months follow-up, resolution of anemia and pulmonary infiltrates were observed. Conclusion: Although the association is rare, celiac disease should be considered in a patient with idiopathic pulmonary hemosiderosis. In our case, severe anemia and alveolar infiltrates markedly improved with glucocorticoids and gluten-free diet. Abbreviations: APTT: activated partial thromboplastin time; BAL: bronchoalveolar lavage; CD: celiac disease; Cd: crypt depth; GFD: gluten-free diet; GI: gastrointestinal; IEL: intraepithelial lymphocyte; INR: international normalized ratio; IPH: idiopathic pu


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