A diagnosis not to be missed: Behcet’s disease as a cause of dilated cardiomyopathy in a young Arab male patient
We report a 33‐year‐old Arab male patient who was thought to have severe idiopathic dilated cardiomyopathy (DCM) associated with complete atrioventricular block for more than 6 years, then was found to possess features suggestive of underlying Behcet’s disease in the form of recurrent oral and genit...
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Veröffentlicht in: | International journal of rheumatic diseases 2010-02, Vol.13 (1), p.97-99 |
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Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | We report a 33‐year‐old Arab male patient who was thought to have severe idiopathic dilated cardiomyopathy (DCM) associated with complete atrioventricular block for more than 6 years, then was found to possess features suggestive of underlying Behcet’s disease in the form of recurrent oral and genital ulcers, cutaneous folliculitis, superficial thrombophlebitis, pathergism, partially thrombosed portal vein and a positive human leukocyte antigen ‐B51. |
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ISSN: | 1756-1841 1756-185X |
DOI: | 10.1111/j.1756-185X.2009.01451.x |