Oral Pyoderma Gangrenosum: Diagnosis, Treatment and Challenges: A Systematic Review

被引:18
作者
Bissonnette C. [1 ]
Kauzman A. [2 ]
Mainville G.N. [2 ]
机构
[1] Resident, Multidisciplinary Residency Program, Faculty of Dentistry, Universite de Montreal, Montreal, QC
[2] Oral and Maxillofacial Pathologist, Department of Stomatology, Faculty of Dentistry, Universite de Montreal, Montreal, QC
关键词
Oral; Oropharyngeal; Persistent oral ulcer; Pyoderma gangrenosum;
D O I
10.1007/s12105-017-0804-3
中图分类号
学科分类号
摘要
Pyoderma gangrenosum (PG) is a distinctive ulcerative skin disorder of unknown etiology, associated with an underlying systemic disease in up to 70% of cases. The condition is characterized by the appearance of one or more necrotic ulcers with a ragged undermined violaceous border and surrounding erythema. Lesions are often initiated by minor trauma. The condition can affect any anatomical site, however the head and neck are rarely involved. Although the oral cavity is subject to recurrent minor trauma through everyday activities such as mastication and oral hygiene, as well as during dental treatment, oral lesions appear to be extremely rare. In an effort to provide a detailed explanation of the oral manifestations of PG, a systematic search was conducted using medical databases. A total of 20 cases of PG with oral involvement were reported in the English and French literature. The objectives of this article are to present the pertinent diagnostic criteria and to discuss the differential diagnosis and therapeutic modalities. © 2017, Springer Science+Business Media New York.
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页码:427 / 441
页数:14
相关论文
共 62 条
  • [1] Powell F.C., Schroeter A.L., Su W.P., Perry H.O., Pyoderma gangrenosum: a review of 86 patients, Q J Med, 55, 217, pp. 173-186, (1985)
  • [2] Su W.P., Davis M.D., Weenig R.H., Powell F.C., Perry H.O., Pyoderma gangrenosum: clinicopathologic correlation and proposed diagnostic criteria, Int J Dermatol, 43, 11, pp. 790-800, (2004)
  • [3] von den Driesch P., Pyoderma gangrenosum: a report of 44 cases with follow-up, Br J Dermatol, 137, 6, pp. 1000-1005, (1997)
  • [4] Kiran R.P., O'Brien-Ermlich B., Achkar J.P., Fazio V.W., Delaney C.P., Management of peristomal Pyoderma gangrenosum, Dis Colon Rectum, 48, 7, pp. 1397-1403, (2005)
  • [5] Setterfield J.F., Shirlaw P.J., Challacombe S.J., Black M.M., Pyoderma gangrenosum associated with severe oropharyngeal involvement and IgA paraproteinaemia, Br J Dermatol, 144, 2, pp. 393-396, (2001)
  • [6] Lazarus G.S., Goldsmith L.A., Rocklin R.E., Pinals R.S., de Buisseret J.P., David J.R., Pyoderma gangrenosum, altered delayed hypersensitivity and polyarthritis, Arch Dermatol, 105, 1, pp. 46-51, (1972)
  • [7] Powell F.C., Su W.P., Perry H.O., Pyoderma gangrenosum: classification and management, J Am Acad Dermatol, 34, 3, pp. 395-409, (1996)
  • [8] Braswell S.F., Kostopoulos T.C., Ortega-Loayza A.G., Pathophysiology of Pyoderma gangrenosum (PG): an updated review, J Am Acad Dermatol, 73, 4, pp. 691-698, (2015)
  • [9] Bhat R.M., Pyoderma gangrenosum: An update, Indian Dermatol Online J, 3, 1, pp. 7-13, (2012)
  • [10] Yco M.S., Warnock G.R., Cruickshank J.C., Burnett J.R., Pyoderma gangrenosum involving the head and neck, Laryngoscope, 98, 7, pp. 765-768, (1988)