S. Civitelli et al., PAPILLARY THYROID-CARCINOMA IN 3 SIBLINGS WITH FAMILIAL ADENOMATOUS POLYPOSIS, International journal of colorectal disease, 11(1), 1996, pp. 34-37
The authors report three siblings (two sisters and their aunt, aged 20
, 22 and 36, respectively) with familial adenomatous polyposis (FAP) a
nd papillary thyroid carcinoma. After diagnosis of FAP, a single, non
palpable nodule was revealed in each patient by routine screening ultr
asonography of the gland, The diagnosis of papillary carcinoma was mad
e by fine-needle-aspiration biopsy of the nodules and confirmed by his
tologic examination of surgical specimens. A review of the literature
reveals about 40 reports of such an association, that is considered no
t fortuitous. Nevertheless, in this family the association seems to be
a distinctive, clinical feature of the syndrome, affecting three out
of five members intensively screened for extracolonic lesions.