An extremely rare manifestation of Behcet's disease: urethrovaginal fistula.
Summary of "An extremely rare manifestation of Behcet's disease: urethrovaginal fistula."
Behcet's disease (BD) is a rare chronic, relapsing, multisystemic disorder characterized by mucocutaneous, ocular, vascular and central nervous system manifestations. However, the etiopathogenesis of the disease remains unknown, and diagnosis is basically dependent on clinical manifestations. Sometimes BD may be diagnosed with rare clinical entities. Herein, we presented an extremely rare case of urethrovaginal fistula which has been diagnosed as manifestation of BD. After surgical treatment of fistula, there was no complication in 6 months following surgical repair and the follow-up period has been going on.
Department of Urology, Erzincan University School of Medicine, 24040, Erzincan, Turkey, firstname.lastname@example.org.
This article was published in the following journal.
Name: International urology and nephrology
- PubMed Source: http://www.ncbi.nlm.nih.gov/pubmed/23925500
- DOI: http://dx.doi.org/10.1007/s11255-013-0519-7
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Medical and Biotech [MESH] Definitions
Rare chronic inflammatory disease involving the small blood vessels. It is of unknown etiology and characterized by mucocutaneous ulceration in the mouth and genital region and uveitis with hypopyon. The neuro-ocular form may cause blindness and death. SYNOVITIS; THROMBOPHLEBITIS; gastrointestinal ulcerations; RETINAL VASCULITIS; and OPTIC ATROPHY may occur as well.
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