Abstract
Cutaneous lesions consonant with Muir-Torre syndrome strongly suggest hereditary non-polyposis colorectal cancer (HNPCC). Ponti et al. discuss the importance of combining molecular genetic features of the sebaceous neoplasms, including microsatellite instability and immunohistochemistry, with family history, to determine the likelihood of HNPCC. Proof of diagnosis is identification of one of the mismatch repair germline mutations.
| Original language | English |
|---|---|
| Pages (from-to) | 2158-2159 |
| Number of pages | 2 |
| Journal | Journal of Investigative Dermatology |
| Volume | 126 |
| Issue number | 10 |
| DOIs | |
| State | Published - Oct 30 2006 |
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All Science Journal Classification (ASJC) codes
- Dermatology
Cite this
Sebaceous skin lesions as clues to hereditary non-polyposis colorectal cancer. / Lynch, Henry T.; Fusaro, Ramon M.; Lynch, Patrick M.
In: Journal of Investigative Dermatology, Vol. 126, No. 10, 30.10.2006, p. 2158-2159.Research output: Contribution to journal › Review article
}
TY - JOUR
T1 - Sebaceous skin lesions as clues to hereditary non-polyposis colorectal cancer
AU - Lynch, Henry T.
AU - Fusaro, Ramon M.
AU - Lynch, Patrick M.
PY - 2006/10/30
Y1 - 2006/10/30
N2 - Cutaneous lesions consonant with Muir-Torre syndrome strongly suggest hereditary non-polyposis colorectal cancer (HNPCC). Ponti et al. discuss the importance of combining molecular genetic features of the sebaceous neoplasms, including microsatellite instability and immunohistochemistry, with family history, to determine the likelihood of HNPCC. Proof of diagnosis is identification of one of the mismatch repair germline mutations.
AB - Cutaneous lesions consonant with Muir-Torre syndrome strongly suggest hereditary non-polyposis colorectal cancer (HNPCC). Ponti et al. discuss the importance of combining molecular genetic features of the sebaceous neoplasms, including microsatellite instability and immunohistochemistry, with family history, to determine the likelihood of HNPCC. Proof of diagnosis is identification of one of the mismatch repair germline mutations.
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UR - http://www.scopus.com/inward/citedby.url?scp=33748759802&partnerID=8YFLogxK
U2 - 10.1038/sj.jid.5700534
DO - 10.1038/sj.jid.5700534
M3 - Review article
C2 - 16983324
AN - SCOPUS:33748759802
VL - 126
SP - 2158
EP - 2159
JO - Journal of Investigative Dermatology
JF - Journal of Investigative Dermatology
SN - 0022-202X
IS - 10
ER -