1967
DOI: 10.1097/00000658-196709000-00008
|View full text |Cite
|
Sign up to set email alerts
|

Familial Medullary Carcinoma Of The Thyroid

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1

Citation Types

0
8
0
1

Year Published

1968
1968
2013
2013

Publication Types

Select...
10

Relationship

1
9

Authors

Journals

citations
Cited by 71 publications
(9 citation statements)
references
References 30 publications
0
8
0
1
Order By: Relevance
“…Several reports have demonstrated familial aggregation of medullary thyroid carcinoma, either in isolation or as part of a multiple endocrine neoplastic syndrome. 45,46 Anthropometric measures have not been included in the majority of thyroid-cancer studies. Dal Maso et al 24 reported that both height and weight were moderately related to thyroid cancer risk.…”
Section: Discussionmentioning
confidence: 99%
“…Several reports have demonstrated familial aggregation of medullary thyroid carcinoma, either in isolation or as part of a multiple endocrine neoplastic syndrome. 45,46 Anthropometric measures have not been included in the majority of thyroid-cancer studies. Dal Maso et al 24 reported that both height and weight were moderately related to thyroid cancer risk.…”
Section: Discussionmentioning
confidence: 99%
“…Of note, the F/M IRR for medullary carcinoma was 3.73, much higher than the 1.31 in SEER. The higher medullary rate among females in Sao Paulo than in SEER, in contrast to similar rates among males, is also notable, especially because a genetic origin has been suggested for these tumors (10,50). Further research is required to investigate a possible genetic susceptibility in Sao Paulo females.…”
Section: Thyroid Cancer Incidence Trend In Sao Paulo and Seermentioning
confidence: 94%
“…Whereas about 20% of medullary thyroid car cinomas are familial [1,2], nonmedullary thyroid car cinomas were thought to be entirely sporadic until recent clinical reports suggested a familial tendency. Some of the familial occurrences were linked to in herited syndromes, such as polyposis coli (Gardner's syndrome) and multiple endocrine neoplasia (type 1), but others reviewed in table 1 [3][4][5][6][7][8][9][10][11][12][13][14][15][16][17][18][19] have occurred without evidence of underlying syndromes.…”
Section: Introductionmentioning
confidence: 99%