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A Behçet-like disease presenting as ulcerative stomatitis and scarring pustular lesions of the face.
Cutis. 1997 Feb; 59(2):74-6.C

Abstract

Behçet's disease is a complex multisystem disease of unknown origin. It presents clinically as oral, pharyngeal, and genital ulcerations, uveitis, and inflammatory papulopustules. Diagnosis is made clinically since laboratory and histologic observations are not specific. We present a patient who, despite the absence of eye and genital lesions, seems best viewed as having Behçet's disease.

Authors+Show Affiliations

Shelley WB
Department of Medicine, Medical College of Ohio, Toledo 43699-0008, USA.
Freimer EH
No affiliation info available
Shelley ED
No affiliation info available

MeSH

AdolescentBehcet SyndromeBiopsy, NeedleDiagnosis, DifferentialFacial DermatosesFemaleGingivitis, Necrotizing UlcerativeHumansSkin Diseases, Vesiculobullous

Pub Type(s)

Case Reports
Journal Article

Language

eng

PubMed ID

9040975

Citation

Shelley, W B., et al. "A Behçet-like Disease Presenting as Ulcerative Stomatitis and Scarring Pustular Lesions of the Face." Cutis, vol. 59, no. 2, 1997, pp. 74-6.
Shelley WB, Freimer EH, Shelley ED. A Behçet-like disease presenting as ulcerative stomatitis and scarring pustular lesions of the face. Cutis. 1997;59(2):74-6.
Shelley, W. B., Freimer, E. H., & Shelley, E. D. (1997). A Behçet-like disease presenting as ulcerative stomatitis and scarring pustular lesions of the face. Cutis, 59(2), 74-6.
Shelley WB, Freimer EH, Shelley ED. A Behçet-like Disease Presenting as Ulcerative Stomatitis and Scarring Pustular Lesions of the Face. Cutis. 1997;59(2):74-6. PubMed PMID: 9040975.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - A Behçet-like disease presenting as ulcerative stomatitis and scarring pustular lesions of the face. AU - Shelley,W B, AU - Freimer,E H, AU - Shelley,E D, PY - 1997/2/1/pubmed PY - 1997/2/1/medline PY - 1997/2/1/entrez SP - 74 EP - 6 JF - Cutis JO - Cutis VL - 59 IS - 2 N2 - Behçet's disease is a complex multisystem disease of unknown origin. It presents clinically as oral, pharyngeal, and genital ulcerations, uveitis, and inflammatory papulopustules. Diagnosis is made clinically since laboratory and histologic observations are not specific. We present a patient who, despite the absence of eye and genital lesions, seems best viewed as having Behçet's disease. SN - 0011-4162 UR - https://www.unboundmedicine.com/medline/citation/9040975/A_Beh������et_like_disease_presenting_as_ulcerative_stomatitis_and_scarring_pustular_lesions_of_the_face_ L2 - http://www.diseaseinfosearch.org/result/780 DB - PRIME DP - Unbound Medicine ER -