Intestinal carcinoid tumours in a father and daughter

Familiar cases of carcinoid tumours that are not associated with any known syndrome or disease are extremely rare. All cases reported in the world lit erature have involved carcinoid rumours of the gastrointestinal tract. Two cases of carcinoid rumours of the small intestine in a father and daughter are presented. Laboratory analyses did not support the hypothesis that the occurrence of carcinoid tumours in this family is a variant of the multiple endocrine neoplasia type I syndrome. A review of the literature on familia l occurrence of intestinal carcinoid rumours in the absence of any other kn own carcinoid tumour-predisposing genetic syndrome is provided.