Title of article :
A case report of a right ventricular mass in a patient with Behc¸et’s disease: Myxoma or thrombus?
Author/Authors :
Ghori, M.A. Sheikh Khalifa Medical City - Department of Cardiac Sciences, Adult Cardiology Department, United Arab Emirates , Al Sousi, Awatif Sheikh Khalifa Medical City - Department of Cardiac Sciences, Adult Cardiology Department, United Arab Emirates , Al Mahmeed, Wael Sheikh Khalifa Medical City - Department of Cardiac Sciences, Adult Cardiology Department, United Arab Emirates , Ellahham, Samer Sheikh Khalifa Medical City - Department of Cardiac Sciences, Adult Cardiology Department, United Arab Emirates , Ayman, Moataz Sheikh Khalifa Medical City - Department of Cardiac Sciences,Cardiac Surgery Department, United Arab Emirates , Augustin, Norbert Sheikh Khalifa Medical City - Department of Cardiac Sciences,Cardiac Surgery Department, United Arab Emirates
From page :
85
To page :
89
Abstract :
Introduction: Behçet’s disease (BD) is a multi-system, chronic and relapsing disorder classified as ‘‘vasculitic syndrome’’. It typically affects young adult females between 20 and 40 years of age. There are some typical clinical manifestations associated with this disease, however, at times; rare sign and symptoms pose a challenge to the treating physician and making a definitive diagnosis. Presentations with cardiac symptoms are one of the extremely rare manifestations of the Behçet’s disease. Methods: The authors present clinical, laboratory and imaging findings of a patient who presented with a cardiac mass which was the first presenting feature or manifestation of Behc¸et’s disease. Results: A 19-year-old boy was admitted to our hospital for the investigation of ‘‘fever of unknown origin’’, weight loss, shortness of breath and a scrotal ulcer of recent on-set. X-ray chest and electrocardiograms were inconclusive. Transthoracic echocardiography revealed a right ventricular (RV) mass attached to the interventricular septum measuring 1.5 x 1.5 cms (Panel A). Cardiac MRI identified it as a RV Myxoma. In addition, on CT scan of the chest pulmonary embolism was noted. The patient underwent excision biopsy of the tumor under cardiopulmonary bypass via right atriotomy (Panel B). Histopathology of the mass described it as ‘‘an organizing thrombus with a few groups of interrupted myocardial fibers and some infiltration of lymphocytes and plasma cells’’. Moreover his HLA typing was found positive for HLA-B51 (5). In view of the above findings and associated lesions, the patient was diagnosed as a case of Behc¸et’s disease. The medical management included immunosuppressant and anticoagulation. Conclusion: Behc¸et’s disease, even in the absence of the typical clinical features, should be considered in the differential diagnosis of right ventricular mass, especially when dealing with young adults from the Mediterranean basin and the Middle-East.
Keywords :
Right ventricular mass , Scrotal ulcer , Behçet’s disease , HLA , B , B51(5)
Journal title :
journal of the saudi heart association
Journal title :
journal of the saudi heart association
Record number :
2657379
Link To Document :
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