Pregled bibliografske jedinice broj: 891173
Right ventricular thrombi – suspicion of arrhythmogenic right ventricular dysplasia: a case report
Right ventricular thrombi – suspicion of arrhythmogenic right ventricular dysplasia: a case report // Cardiologia croatica// 8. hrvatski ehokardiografski skup s međunarodnim sudjelovanjem / Radna skupina za ehokardiografiju i slikovne metode u kardiologiji Hrvatskoga kardiološkog društva (ur.).
Zagreb: Hrvatsko kardiološko društvo, 2015. str. 81-82 (predavanje, nije recenziran, sažetak, stručni)
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Naslov
Right ventricular thrombi – suspicion of arrhythmogenic right ventricular dysplasia: a case report
Autori
Sušić, Livija ; Baraban, Vedrana ; Vincelj, Josip ; Ćatić, Jasmina ; Blažeković, Robert
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, stručni
Izvornik
Cardiologia croatica// 8. hrvatski ehokardiografski skup s međunarodnim sudjelovanjem
/ Radna skupina za ehokardiografiju i slikovne metode u kardiologiji Hrvatskoga kardiološkog društva - Zagreb : Hrvatsko kardiološko društvo, 2015, 81-82
Skup
CroEcho 2015
Mjesto i datum
Opatija, Hrvatska, 2015
Vrsta sudjelovanja
Predavanje
Vrsta recenzije
Nije recenziran
Ključne riječi
dyspnea, syncope, cardiac arrhythmia, thrombus, arrythmogenic right ventricular cardiomyopathy
Sažetak
CASE REPORT: 61-year-old woman with long history of hypertension presented with progressive dyspnea and chest pain that she has been experiencing at minor physical exertion for several months. Current medical records confirmed T-wave inversion in right precordial leads, attacks of supraventricular and ventricular arrhythmia, including attacks of non-sustained ventricular tachycardia and reccurent syncopal episodes from the age of 23. Dilated right heart chamber are detected by transthoracic echocardiogram year 2006, presence of the shunt was excluded by scintigraphy. Imaging studies: 2-dimensional transthoracic echocardiogram revealed one large (Figure 1) and two smaller hyperechogenic masses (Figure 2) inside extremely dilated (Figure 3) and globally hypokinetic right ventricle with moderate tricuspid regurgitation. 3-dimensional transesophageal echocardiogram confirmed mobile pedunculated mass by free wall of right ventricle (Figure 4). Magnetic resonance imaging describe dilated right heart chambers, hypertrophic septomarginal trabeculae of the mid-apical part of right ventricular and mass within the same chamber appears to be a tumour. CT pulmonary angiogram, PET CT and coronarography ruled out specific pathomorphological substrate. Treatment: Three large individual masses were surgically removed from the chamber of right ventricle (Figure 5). Annuloplasty of the tricuspid valve was performed. Pathohistological diagnosis: focal-organizing thrombi. Conclusion: Although final diagnosis has not been made, it is possible that the patient suffers from arrhythmogenic right ventricular dysplasia. This conclusion is based on the presence of three big McKenna’s criteria T-wave inversion in right precordial leads, ECHO-PLAX RVOT >32 mm and non- sustained ventricular tachycardia detected during Holter monitoring) and the fact that literary sources describe several cases of thrombotic masses in right heart chambers in patients with the same diagnosis.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
POVEZANOST RADA
Ustanove:
Klinička bolnica "Dubrava",
Medicinski fakultet, Osijek