Abstract
A kindred in which five first-degree relatives were initially known to exhibit colorectal, endometrial, and unspecified carcinoma for two generations, occurring at an early age and including three cases of multiple primary cancer, is consistent with criteria for the cancer family syndrome. Follow-up included a diligent surveillance program that led to the early diagnosis of colon cancer in a young member of the third generation who had been considered at high risk for this lesion. Manifestly, hereditary cancer syndrome identification may be expedited through longitudinal study of apparently cancer-prone kindreds, given limited historical information about tumor expression. However, cancer surveillance measures can and should be instituted early and predicated on clues that suggest, but need not be diagnostic of, such a hereditary cancer predisposing disorder.
| Original language | English |
|---|---|
| Pages (from-to) | 535-538 |
| Number of pages | 4 |
| Journal | JAMA - Journal of the American Medical Association |
| Volume | 240 |
| Issue number | 6 |
| DOIs | |
| State | Published - Aug 11 1978 |
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All Science Journal Classification (ASJC) codes
- Medicine(all)
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Minimal Genetic Findings and Their Cancer Control Implications : A Family With the Cancer Family Syndrome. / Lynch, Henry T.; Lynch, Patrick M.; Harris, Randall E.
In: JAMA - Journal of the American Medical Association, Vol. 240, No. 6, 11.08.1978, p. 535-538.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Minimal Genetic Findings and Their Cancer Control Implications
T2 - A Family With the Cancer Family Syndrome
AU - Lynch, Henry T.
AU - Lynch, Patrick M.
AU - Harris, Randall E.
PY - 1978/8/11
Y1 - 1978/8/11
N2 - A kindred in which five first-degree relatives were initially known to exhibit colorectal, endometrial, and unspecified carcinoma for two generations, occurring at an early age and including three cases of multiple primary cancer, is consistent with criteria for the cancer family syndrome. Follow-up included a diligent surveillance program that led to the early diagnosis of colon cancer in a young member of the third generation who had been considered at high risk for this lesion. Manifestly, hereditary cancer syndrome identification may be expedited through longitudinal study of apparently cancer-prone kindreds, given limited historical information about tumor expression. However, cancer surveillance measures can and should be instituted early and predicated on clues that suggest, but need not be diagnostic of, such a hereditary cancer predisposing disorder.
AB - A kindred in which five first-degree relatives were initially known to exhibit colorectal, endometrial, and unspecified carcinoma for two generations, occurring at an early age and including three cases of multiple primary cancer, is consistent with criteria for the cancer family syndrome. Follow-up included a diligent surveillance program that led to the early diagnosis of colon cancer in a young member of the third generation who had been considered at high risk for this lesion. Manifestly, hereditary cancer syndrome identification may be expedited through longitudinal study of apparently cancer-prone kindreds, given limited historical information about tumor expression. However, cancer surveillance measures can and should be instituted early and predicated on clues that suggest, but need not be diagnostic of, such a hereditary cancer predisposing disorder.
UR - http://www.scopus.com/inward/record.url?scp=0018161249&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0018161249&partnerID=8YFLogxK
U2 - 10.1001/jama.1978.03290060037009
DO - 10.1001/jama.1978.03290060037009
M3 - Article
C2 - 671663
AN - SCOPUS:0018161249
VL - 240
SP - 535
EP - 538
JO - JAMA - Journal of the American Medical Association
JF - JAMA - Journal of the American Medical Association
SN - 0002-9955
IS - 6
ER -