2011
DOI: 10.1016/j.crohns.2010.10.001
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An unusual case of Crohn's disease with isolated gastric involvement

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Cited by 8 publications
(4 citation statements)
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“…This is not unique among upper gastrointestinal Crohn's disease cases; however, this case is unlike other cases to our knowledge due to the rapid onset of symptoms of gastric outlet obstruction with no long history of gastritis-like symptoms. Documented cases of isolated upper gastrointestinal Crohn's disease typically present with gastritis-like epigastric pain progressing over a number of years [ 7 9 ]. Symptoms of gastric outlet obstruction (bloating, vomiting, postprandial pain and weight loss) evolve in many cases, but almost universally after years of gastritis-like symptoms.…”
Section: Discussionmentioning
confidence: 99%
“…This is not unique among upper gastrointestinal Crohn's disease cases; however, this case is unlike other cases to our knowledge due to the rapid onset of symptoms of gastric outlet obstruction with no long history of gastritis-like symptoms. Documented cases of isolated upper gastrointestinal Crohn's disease typically present with gastritis-like epigastric pain progressing over a number of years [ 7 9 ]. Symptoms of gastric outlet obstruction (bloating, vomiting, postprandial pain and weight loss) evolve in many cases, but almost universally after years of gastritis-like symptoms.…”
Section: Discussionmentioning
confidence: 99%
“…Gastroduodenal CD is reported in 0.5 to 4.0% of all CD cases ( 8–11 ). Isolated gastric involvement is rare, affecting less than 0.07% of all CD cases ( 12 ). Almost 60% of patients with gastroduodenal CD have had previous inflammation elsewhere in the GI tract, and one-third of patients with isolated upper GI CD (UGI-CD) at diagnosis will develop distal disease later in life ( 8 , 10 , 13 ).…”
Section: Review Of Literaturementioning
confidence: 99%
“…UGI-CD is diagnosed based on a combination of clinical presentation, biochemical signs of inflammation, and endoscopic evaluation with biopsy and histopathological evaluation ( 12 , 15 ). Nugent and Roy grouped these investigations and formulated diagnostic criteria for gastroduodenal CD: (1) demonstration of non-caseating granulomatous inflammation in the stomach or duodenum in the absence of other systemic granulomatous disorders, with or without more distal intestinal inflammation; (2) endoscopic or radiographic findings of diffuse inflammation in the stomach or duodenum consistent with CD in a patient with confirmed CD of the GI tract ( 11 ).…”
Section: Review Of Literaturementioning
confidence: 99%
“…Gastroduodenal CD affects 0.5–4% of all CD patients [ 4 ], with the majority of such patients having concurrent involvement of the colon with isolated gastroduodenal involvement accounting for less than 0.07% of all CD patients [ 5 , 6 ]. Pathology is more obscure in the upper GI tract, and noncaseating granulomas are not necessarily needed for confirmatory diagnosis.…”
Section: Introductionmentioning
confidence: 99%