PMID- 23286810
OWN - NLM
STAT- MEDLINE
DCOM- 20130617
LR  - 20130104
IS  - 1087-2108 (Electronic)
IS  - 1087-2108 (Linking)
VI  - 18
IP  - 12
DP  - 2012 Dec 15
TI  - Angiofibromas in multiple endocrine neoplasia type 1.
PG  - 20
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.
FAU - Vashi, Neelam
AU  - Vashi N
AD  - The Ronald O. Perelman Department of Dermatology, New York University School of 
      Medicine, USA.
FAU - Hunt, Raegan
AU  - Hunt R
FAU - Fischer, Max
AU  - Fischer M
FAU - Meehan, Shane
AU  - Meehan S
FAU - Pomeranz, Miriam Keltz
AU  - Pomeranz MK
LA  - eng
PT  - Case Reports
PT  - Journal Article
DEP - 20121215
PL  - United States
TA  - Dermatol Online J
JT  - Dermatology online journal
JID - 9610776
SB  - IM
MH  - Adult
MH  - Angiofibroma/*pathology
MH  - Female
MH  - Humans
MH  - Multiple Endocrine Neoplasia Type 1/*genetics
MH  - Nose Neoplasms/pathology
MH  - Skin Neoplasms/*pathology
MH  - Thorax
EDAT- 2013/01/05 06:00
MHDA- 2013/06/19 06:00
CRDT- 2013/01/05 06:00
PHST- 2013/01/05 06:00 [entrez]
PHST- 2013/01/05 06:00 [pubmed]
PHST- 2013/06/19 06:00 [medline]
PST - epublish
SO  - Dermatol Online J. 2012 Dec 15;18(12):20.