Tamponade revealing hydatid cyst of the left ventricle
Rim Ouazzane, Gaelle Minko, Isis Azannai, Marwa Abdulhakeem, Rachida Habbal
Corresponding author: Rim Ouazzane, University Hospital Ibnrochd, Casablanca, Morrocco
Received: 19 Nov 2019 - Accepted: 27 Nov 2019 - Published: 30 Nov 2019
Domain: Cardiology
Keywords: Cardiac hydatid, tamponade, left ventricule
©Rim Ouazzane 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: Rim Ouazzane et al. Tamponade revealing hydatid cyst of the left ventricle. PAMJ Clinical Medicine. 2019;1:35. [doi: 10.11604/pamj-cm.2019.1.35.21032]
Available online at: https://www.clinical-medicine.panafrican-med-journal.com//content/article/1/35/full
Tamponade revealing hydatid cyst of the left ventricle
Rim Ouazzane1,&, Gaelle Minko1, Isis Azannai1, Marwa Abdulhakeem1, Rachida Habbal1
1University Hospital Ibnrochd, Casablanca, Morrocco
&Corresponding author
Rim Ouazzane, University Hospital Ibnrochd, Casablanca, Morrocco
The hydatid disease is endemic in certain areas of the world such as the Mediterranean basin. We report the observation of cardiac hydatidosis revealed by pericardial effusion. A 49 year old man, with no particular pathological antecedents, consulted for progressive dyspnea since 3 months. In cardiac echocardiography, we noticed the presence of an abundant pericardial effusion in pre-tamponade. A pericardial puncture indicated urgently was performed. Thoracoabdominal CT scan showed a multivesicular hydatious cyst of type 3 interesting the superior part of the left ventricle. The patient was put on medical treatment (Albendazole®) and referred to surgery for management.
The hydatid disease or hydatid cyst results from the development of the hydatid larvae of a taenia echinococcus or echinococcus granulosus. It is endemic in certain areas of the world such as the Mediterranean basin. We report the observation of cardiac hydatidosis revealed by pericardial effusion.
A 49 year old man, with no particular pathological antecedents, consulted for progressive dyspnea since 3 months. In physical examination, blood pressure was 100/60 mmHg, respiratory rate 24/min and pulse rate 98/min. Cardiovascular examination showed Muffling of heart sounds with no signs of heart failure. The rest of the clinical examination was normal. The electrocardiogram showed a right bundle of branches Chest X-ray showed a cardiomegaly. (Figure 1) In cardiac echocardiography, we noticed the presence of an abundant pericardial effusion in pre-tamponade. A pericardial puncture indicated urgently was performed and had removed 1100ml of exudative yellow liquid citrin. Thoracoabdominal CT scan showed a multivesicular hydatid cyst of type 3 interesting the superior part of the left ventricle and another hydatic cyst of 8cm interesting segment 8 of the liver of type 4. There was no pulmonary involvement associated. (Figure 2) The patient was put on medical treatment (Albendazole®), and referred to surgery for management.
The cardiac hydatid cyst is rare, representing 0.5% to 2% of all hydatid locations. The literature review showed the predominance of the left ventricular location of the hydatid cyst (60%) which is explained by the importance of muscle mass and the rich vascularization of the left ventricle [1]. The interventricular septum is affected in 9 to 20% of cases, while the right ventricle and the right atrium (4 to 17%) and the interatrial septum (2%) [2]. The circumstances of discovery are numerous, the symptomatology varies according to the evolutionary stage of the cyst and its seat. Complications are mainly represented by pulmonary embolism, systemic, cerebral, valvular obstruction, atrioventricular block or rupture in the pericardium [3]. Echocardiography remains the key examination for the diagnosis of cardiac hydatid disease. CT and MRI allow more accurate topographic analysis and study of cyst ratios. The curative treatment of cardiac hydatidosis is exclusively surgical. It is systematic and must be done as early as possible to prevent the occurrence of complications.
The cardiac hydatid cyst is a serious and rare pathology. The clinical pictures are variable and nonspecific. The therapeutic management is delicate and combines medical treatment to surgery.
The authors declare no competing interests.
All the authors have read and agreed to the final manuscript.
Figure 1: frontal chest image showing cardiomegaly and bulging of the left lower arch
Figure 2: CT scan mediastinal window showing a type 3 multivesicular cyst sitting in the left ventricle
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