Adult patent ductus arteriosus complicated by pulmonary infective endocarditis
Abdelmjid El Adaoui, Rime Benmalek
Corresponding author: Rime Benmalek, Resident in Department of Cardiology, Hospital University Center Ibn Rochd, Casablanca, Morocco
Received: 02 Jun 2020 - Accepted: 24 Jul 2020 - Published: 05 Aug 2020
Domain: Cardiology
Keywords: Patent ductus arteriosus, pulmonary infective endocarditis, adult
©Abdelmjid El Adaoui et al. PAMJ Clinical Medicine (ISSN: 2707-2797). This is an Open Access article distributed under the terms of the Creative Commons Attribution International 4.0 License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Cite this article: Abdelmjid El Adaoui et al. Adult patent ductus arteriosus complicated by pulmonary infective endocarditis. PAMJ Clinical Medicine. 2020;3:161. [doi: 10.11604/pamj-cm.2020.3.161.23956]
Available online at: https://www.clinical-medicine.panafrican-med-journal.com//content/article/3/161/full
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Adult patent ductus arteriosus complicated by pulmonary infective endocarditis
Adult patent ductus arteriosus complicated by pulmonary infective endocarditis
Abdelmjid El Adaoui1, Rime Benmalek1,&
&Corresponding author
We report the case of a 32-year-old male with Down Syndrome and a medical history of Immune thrombocytopenia (ITP) under corticosteroids, who was admitted to the cardiology department for prolonged fever and asthenia. On inspection, the conjunctivae were anemic and physical examination found a febrile patient (38.9°C) and a 3/6 continuous murmur in the pulmonary area. Blood tests revealed a normocystic, normochromic anemia (Hemoglobin 8.6 g/dL) and severe thrombocytopenia (9000/mm3), a leukocyte count of 12,500 cells/mm3, and high C-reactive protein and erythrocyte sedimentation rates. Thoracic X-ray showed cardiomegaly with normal lung area. Transthoracic Echocardiography (TEE) was immediately performed and showed a 7 mm Patent ductus arteriosus (PDA) associated to a large oscillating mobile vegetation attached to the pulmonic valve measuring 32 x 15 mm (A,B,C,D) with a dilated pulmonary artery and a severe pulmonary insufficiency. Right chambers were dilated (RV infundibulum = 37mm, RV basal diameter = 46 mm, RA surface= 24 cm2) with moderate tricuspid regurgitation and a transvalvular gradient of 68 mmHg, left valves were normal. Repeated blood cultures were sterile, empirical antibiotherapy including vancomycin and gentamycin was started with no significant improvement after 2 weeks. The patient underwent surgical vegectomy with pulmonic and tricuspid valves´ repair, and closure of PDA was not considered. Post-operative period was uneventful, after 2 additional weeks of antibiotherapy, the evolution was favorable with apyrexia, inflammation markers normalization and no residual vegetation in the post-operative TTE. The patient was discharged from hospital as he was asymptomatic and was advised regular follow up.
Figure 1: transthoracic echocardiography showing (A) large highly mobile pulmonic valve vegetation measuring 32X15 mm (B) with dilated pulmonary artery and right ventricule infundibulum (C) and a 7 mm patent ductus arteriosus (D) and severe pulmonary regurgitation