Abstract
We report the case of a 13-year-old girl with no particular medical history who presented with an anemic syndrome with weight stagnation associated with epigastralgia and transit disorders. The blood count confirmed the presence of a hypochromic microcytic anemia, and digestive exploration by oeso-gastroduodenal endoscopy revealed gastritis. The biopsy with histological analyses has revealed a chronic atrophic gastritis in favor of Biermer's disease. The Helicobacter pylori test was negative. The immunological exploration found a high level of anti-parietal cell antibodies confirming the diagnosis of Biermer's disease. Poorly described in children, Biermer's disease presents in our case a particular form due to the atypical clinical presentation different from the usual form described in the literature which usually associated macrocytic anemia and vitamin B12 deficiency.
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