TY - JOUR
T1 - Angiofibromas in multiple endocrine neoplasia type 1
AU - Vashi, Neelam
AU - Hunt, Raegan
AU - Fischer, Max
AU - Meehan, Shane
AU - Pomeranz, Miriam Keltz
PY - 2012/12
Y1 - 2012/12
N2 - Multiple endocrine neoplasia type 1 (MEN1) is a familial tumor syndrome with autosomal dominant inheritance. Cutaneous tumors in MEN1, which include multiple angiofibromas, collagenomas, and lipomas can easily be overlooked because of their subtle appearance. As markers of this tumor syndrome, recognition of the mucocutaneous manifestations of MEN1 is important in order to facilitate early interdisciplinary care and diagnosis of associated internal disease in both patients and family members.
AB - Multiple endocrine neoplasia type 1 (MEN1) is a familial tumor syndrome with autosomal dominant inheritance. Cutaneous tumors in MEN1, which include multiple angiofibromas, collagenomas, and lipomas can easily be overlooked because of their subtle appearance. As markers of this tumor syndrome, recognition of the mucocutaneous manifestations of MEN1 is important in order to facilitate early interdisciplinary care and diagnosis of associated internal disease in both patients and family members.
UR - http://www.scopus.com/inward/record.url?scp=84871527463&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84871527463&partnerID=8YFLogxK
M3 - Article
C2 - 23286810
AN - SCOPUS:84871527463
SN - 1087-2108
VL - 18
SP - 20
JO - Dermatology Online Journal
JF - Dermatology Online Journal
IS - 12
ER -