Abstract
We report of a 13-7/12 year old boy with congenital pernicious anemia. His first anemic episode was seen at 1-8/12 year old. His anemia responded well to the therapy of vitamin B12 and folic acid, and improved dramatically. Thereafter, he had been symptomless for about 12 years untill a month prior to this visit and admission to our clinic.
He had atrophic gastric mucosa with normal gastric acid secretion and transitory selective malabsorption of vitamin B12. Both of these findings are different from those of typical case with congenital pernicious anemia, and possibly derived from the prolonged vitamin B12 deficiency.
We would like to follow carefully whether he will develop to other types of pernicious anemia associated with achlorhydria, and/or with antibodies to the intrinsic factor or to the parietal cells.