De ziekte van Behcet

Translated title of the contribution: Behcet's disease

H. Ten Hoopen-Neumann, W. I. Van Der Meijden, P. M. Van Hagen*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

9 Citations (Scopus)

Abstract

Three women aged 30, 38 and 34 years, originating from Morocco, the Dominican Republic and Turkey, had been suffering since several years from, among other things, oral aphthae, vaginal ulcers and skin lesions without specific abnormalities at examination of blood and biopsies. The diagnosis of Behcet's disease was made and immunomodulating treatment instituted, following which the patients improved. Behcet's disease is a chronic inflammatory multisystemic disorder of unknown aetiology. Originally it was characterised as a triad of recurrent oral aphthae, genital ulcers and inflammatory eye disease. Because symptoms manifest themselves over many years the disease can be missed or misdiagnosed easily. There is no laboratory test available to support the diagnosis, so that the diagnosis is based on clinical symptomatology. The incidence is increasing due to migration from areas with higher prevalence.

Translated title of the contributionBehcet's disease
Original languageDutch
Pages (from-to)177-180
Number of pages4
JournalNederlands Tijdschrift voor Geneeskunde
Volume143
Issue number4
Publication statusPublished - 23 Jan 1999

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