Behçet's Disease in Childhood: Report of One Case

Yu Yuan Ke, Kao Pin Hwang*, I. Hsien Lee, Chee Yin Chai

*Corresponding author for this work

Research output: Contribution to journalJournal Article peer-review

1 Scopus citations

Abstract

We report on a 6yr 7m-old girl who had suffered from recurrent oral ulcers since July, 2000. Anal ulcers were also noted initially, and arthralgia was observed. Skin testing (pathergy test) showed only mild erythematous changes over the test area. HLA typing revealed HLA-B56. Intestinal symptoms included watery diarrhea with occasional blood. No ocular involvement was found. Her aliment was diagnosed as incomplete Behçet's disease with intestinal involvement. Diagnosis of Behçet's disease in childhood is a challenge and there are only a few studies on juvenile Behçet's disease (JBD) in the literature, with only a small number of patients. According to the literature, Behçet's disease in childhood is characterized by a low incidence of ocular lesion and a high incidence of intestinal involvement, as exhibited in this case.

Original languageEnglish
Pages (from-to)292-296
Number of pages5
JournalZhonghua Minguo xiao er ke yi xue hui za zhi [Journal]. Zhonghua Minguo xiao er ke yi xue hui
Volume44
Issue number5
StatePublished - 09 2003
Externally publishedYes

Keywords

  • Behçet's disease
  • HLA-B56
  • Mucosal ulcer

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