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
Hauptverfasser: AL IZZI, Mustafa, EL BUR, Mohammed, ARIF, Mohammed
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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.
ISSN:1756-1841
1756-185X
DOI:10.1111/j.1756-185X.2009.01451.x