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A rare complication of Behçet’s disease in a 12-year-old girl: a large intracardiac thrombosis

Published online by Cambridge University Press:  15 November 2022

Şenay Akbay
Affiliation:
Pediatric Cardiology, Akdeniz University Medical School, Antalya, Turkey
Filiz Ekici*
Affiliation:
Pediatric Cardiology, Akdeniz University Medical School, Antalya, Turkey
Elif Çomak
Affiliation:
Pediatric Rheumatology, Akdeniz University Medical School, Antalya, Turkey
*
Author for correspondence: Dr F. Ekici, Pediatric Cardiology, Akdeniz University Medical School, Antalya, Turkey. Tel: +0902422496543; Fax: +0902422274320. E-mail: ekicifiliz@gmail.com

Abstract

Behcet’s disease is a multi-systemic inflammatory disease with a clinical spectrum as a triple complex of recurrent oral, genital ulcers, and uveitis. Cardiac involvement in patients with Behcet’s disease is extremely rare and often associated with poor prognosis. Behcet’s disease should be considered in the differential diagnosis of right ventricular mass especially in young adults, even there is no typical clinical features of Behcet’s disease. In this case, a 12-year-old girl who admitted with chest pain and haemoptysis and then was diagnosed with intracardiac thrombus related to Behcet’s disease during follow-up was described.

Type
Brief Report
Copyright
© The Author(s), 2022. Published by Cambridge University Press

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