RT Book, Section
A1 Zouboulis, Christos C.
A2 Kang, Sewon
A2 Amagai, Masayuki
A2 Bruckner, Anna L.
A2 Enk, Alexander H.
A2 Margolis, David J.
A2 McMichael, Amy J.
A2 Orringer, Jeffrey S.
SR Print(0)
ID 1161350001
T1 Adamantiades–Behçet Disease
T2 Fitzpatrick's Dermatology, 9e
YR 2019
FD 2019
PB McGraw-Hill Education
PP New York, NY
SN 9780071837798
LK dermatology.mhmedical.com/content.aspx?aid=1161350001
RD 2024/04/24
AB AT-A-GLANCERare  disease  with  worldwide  distribution  but  strongly  varying  prevalence;  certain  ethnic  groups  are  mainly  affected.A  genetically  determined  disorder  with  a  probable  environmental  triggering  factor.Multisystem  occurrence,  with  oral  aphthous  ulcers,  genital  ulcers,  papulopustules,  erythema  nodosum–like  lesions,  uveitis,  and  arthropathy  as  the  most  common  signs.Inflammatory  disease  representing  a  neutrophilic  vascular  reaction  or  vasculitis.Chronic,  relapsing,  and  progressive  course  with  a  potentially  poor  prognosis  (especially  in  males  with  systemic  presenting  signs;  mortality,  0%-6%).