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*Very rare. | *Very rare. | ||
*APC promotor IB mutations.<ref name=pmid30584346/> | *APC promotor IB mutations.<ref name=pmid30584346/> | ||
*Autosomal dominant inheritance.<ref name=pmid30584346/> | |||
==Criteria== | ==Criteria== | ||
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**Histology predominantly [[fundic gland polyp]]s - some with dysplasia or adenocarcinoma in background. | **Histology predominantly [[fundic gland polyp]]s - some with dysplasia or adenocarcinoma in background. | ||
*No colorectal or duodenal polyposis. | *No colorectal or duodenal polyposis. | ||
*Exclusion of other heritable polyposis syndrome involving the stomach, proton pump inhibitor (PPI) use. | |||
*Exclusion of other heritable polyposis syndrome involving the stomach, PPI use. | |||
==See also== | ==See also== | ||
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[[Category:Diagnosis]] | [[Category:Diagnosis]] | ||
[[Category:Syndromes]] | [[Category:Syndromes]] | ||
[[Category:Stomach]] |
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