2020
DOI: 10.1016/j.ajg.2020.02.001
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Gastric sarcoidosis: Rare revealing feature of systemic sarcoidosis

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Cited by 2 publications
(2 citation statements)
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“…19.5d). Other rare non-infectious causes of GG include tumorous conditions (adenocarcinoma and MALT lymphoma), vasculitides, eosinophilic granulomatosis, polyangiitis, drugs like cocaine, carbimazole and interferon, xanthogranulomatous gastritis, foreign body reactions to stomach contents within an ulcer repair zone or to surgical material (suture granuloma), crystalline drugs (antacids containing magnesium, aluminium and silicon), reaction to endogenous materials (mucin, lipid or crystalline material), Langerhans cell histiocytosis (more common in children) and chronic granulomatous disease (more common in childhood and adolescence) [61][62][63][64][65][66][67][68][69][70]. Clinically apparent gastritis is seen in 2 to 7 percent of CD patients, microscopic involvement may be seen in up to 75 percent of patients in a normal appearing mucosa endoscopically [60].…”
Section: Granulomatous Gastritismentioning
confidence: 99%
“…19.5d). Other rare non-infectious causes of GG include tumorous conditions (adenocarcinoma and MALT lymphoma), vasculitides, eosinophilic granulomatosis, polyangiitis, drugs like cocaine, carbimazole and interferon, xanthogranulomatous gastritis, foreign body reactions to stomach contents within an ulcer repair zone or to surgical material (suture granuloma), crystalline drugs (antacids containing magnesium, aluminium and silicon), reaction to endogenous materials (mucin, lipid or crystalline material), Langerhans cell histiocytosis (more common in children) and chronic granulomatous disease (more common in childhood and adolescence) [61][62][63][64][65][66][67][68][69][70]. Clinically apparent gastritis is seen in 2 to 7 percent of CD patients, microscopic involvement may be seen in up to 75 percent of patients in a normal appearing mucosa endoscopically [60].…”
Section: Granulomatous Gastritismentioning
confidence: 99%
“…The most commonly involved organs are the lung, liver, and lymph nodes. Gastric involvement is reported in less than 1% of patients presenting with systemic sarcoidosis [ 1 ]. Hence, gastric sarcoidosis is a rare entity, and there are only a handful of well-documented histologic pieces of evidence of non-necrotizing granulomas consistent with gastrointestinal (GI) sarcoidosis [ 2 ].…”
Section: Introductionmentioning
confidence: 99%