Dilated Cardiomyopathy in Behcet's Disease in a Young Male Patient

AuthorHamid Khederlouen
AuthorSamin Taherien
AuthorAlireza Sadeghien
AuthorAmirhossein Moghtader Mojdehien
OrcidHamid Khederlou [0000-0001-8606-2381]en
Issued Date2017-10-31en
AbstractBehcet's disease is a multisystemic, inflammatory and chronic disorder characterized by recurrent oral aphthous ulcers and genital ulcers, uveitis and other manifestations, including systemic organ involvement. Cardiac involvement in Behcet's disease is rarely however, it plays an important role in prognosis and increases mortality. We hereby have reported a case of Behcet's disease with dilated cardiomyopathy. He was presented with constitutional symptoms and also oral and genital aphthous ulcers, pseudofolliculitis, tachycardia, arthritis, splenomegaly, ESR (erythrocyte sedimentation rate) and CRP (C-reactive protein) elevation and LV systolic dysfunction with LVEF=45% were found in evaluatien
DOIhttps://doi.org/10.21859/ijcp-030102en
KeywordCardiomyopathiesen
KeywordBehcet Syndromeen
PublisherBrieflandsen
TitleDilated Cardiomyopathy in Behcet's Disease in a Young Male Patienten
TypeCase Reporten

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