1
|
Chigullapalli S, Malani SK, Nalawade D, Musuku MR. Aorto-atrial tunnel arising from sinus of Valsalva aneurysm in a young female. BMJ Case Rep 2024; 17:e259254. [PMID: 38490706 PMCID: PMC10946376 DOI: 10.1136/bcr-2023-259254] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 03/17/2024] Open
Abstract
A young female patient presented with complaints of breathlessness and palpitations since 2 years. On clinical examination, there was a loud continuous murmur at the right sternal border.Transthoracic echocardiography and colour Doppler showed a tunnel-like structure originating from the aneurysmal right coronary sinus and opening into the right atrium with left to right shunt. Coronary angiography revealed a large tunnel beginning in right coronary sinus and terminating in the right atrium and right coronary artery (RCA) was seen originating from the tunnel. Cardiac catheterisation revealed normal pulmonary artery pressure. CT and 3D-reconstructed images delineated the extracardiac course of the tunnel.Various treatment modalities including percutaneous transcatheter approach and surgical treatment were taken into consideration, but because of the close proximity of RCA from the tunnel opening, surgical closure was preferred.
Collapse
Affiliation(s)
- Sridevi Chigullapalli
- Cardiology, Dr D Y Patil Medical College Hospital and Research Centre, Pune, Maharashtra, India
| | - Susheel Kumar Malani
- Cardiology, Dr D Y Patil Medical College Hospital and Research Centre, Pune, Maharashtra, India
| | - Digvijay Nalawade
- Cardiology, Dr D Y Patil Vidyapeeth University Dr D Y Patil Medical College Hospital and Research Centre, Pune, India
| | | |
Collapse
|
2
|
Congenital Aorto-Cardiac Connections (CACC) Revisited: Introduction of a Novel Anatomic-therapeutic Classification. Pediatr Cardiol 2021; 42:1459-1477. [PMID: 34327543 DOI: 10.1007/s00246-021-02671-5] [Citation(s) in RCA: 2] [Impact Index Per Article: 0.5] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 04/05/2021] [Accepted: 06/23/2021] [Indexed: 10/20/2022]
Abstract
Abnormal congenital aorto-cardiac communications (CACC) are a heterogeneous constellation of anomalies that provide an abnormal connection between the aorta and other cardiac chambers or structures, including the atria, ventricles, the main pulmonary artery, and the coronary sinus. The current terminology of CACC has significant errors and shortcomings including inconsistent and interchangeable use of terms of fistula and tunnel and lack of an inclusive classification with practical information on therapeutic management. The aims of this study were threefold: firstly, to perform a concise narrative review of congenital pathologic connections between the aortic root and cardiac chambers which include rupture of congenital sinus of Valsalva aneurysm, aorto-left ventricular and less commonly right ventricular tunnels, coronary cameral fistulas, and aorto-atrial communications; secondly, to investigate the differentiating features of the so-called aorta right atrial tunnel (ARAT), with and without coronary artery take-off from the tunnel, and coronary cameral fistula (CCF) by applying a differential diagnostic assistance toolbox to two groups of patients with ARAT and CCF; and lastly, to propose a practical and inclusive anatomic-therapeutic classification for CACCs. The two main cornerstones of the proposed classification are the type of the connector between the aorta and cardiac chamber (hole versus passage) and the nature of the connecting passage ( anatomic versus extra-anatomic). We classified CACCs into three types. Depending on the intramural versus extramural course of the extra-anatomic connecting passage, type 3 is further subdivided into type 3A and type 3B.
Collapse
|
3
|
Onorato EM, Costante AM, Andreini D, Bartorelli AL. Infective endocarditis of an asymptomatic congenital aorta-right atrial tunnel: a case report. EUROPEAN HEART JOURNAL-CASE REPORTS 2020; 4:1-5. [PMID: 32352048 PMCID: PMC7180523 DOI: 10.1093/ehjcr/ytaa039] [Citation(s) in RCA: 1] [Impact Index Per Article: 0.2] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Download PDF] [Figures] [Subscribe] [Scholar Register] [Received: 11/05/2019] [Revised: 12/19/2019] [Accepted: 01/28/2020] [Indexed: 11/13/2022]
Abstract
Background Aorta-right atrial tunnel (ARAT) is a rare congenital anomaly whose aetiology and incidence are unknown. It might represent a diagnostic and therapeutic challenge requiring a combination of imaging modalities and an integrated teamwork. Case summary We report a case of a 23-year-old man with an asymptomatic ARAT complicated by infective endocarditis, diagnosed with non-invasive multimodality imaging, and successfully treated with a catheter-based approach. Discussion Aorta-right atrial tunnel closure in asymptomatic patients is still a matter of debate. Considering the risk of serious complications surgical treatment might be recommended soon after diagnosis. In selected cases, catheter-based closure might represent a safe, effective, and less invasive alternative to traditional surgical approach.
Collapse
Affiliation(s)
- Eustaquio Maria Onorato
- Centro Cardiologico Monzino, IRCCS, University School of Milan, Via C. Parea, 4, 20138 Milan, Italy
| | - Anna Maria Costante
- Cardiology Department, Azienda Ospedaliera SS. Antonio e Biagio e Cesare Arrigo, Via Venezia 16 - 15121 Alessandria, Italy
| | - Daniele Andreini
- Centro Cardiologico Monzino, IRCCS, University School of Milan, Via C. Parea, 4, 20138 Milan, Italy.,Department of Clinical Sciences and Community Health, Via della Commenda 19 - 20122, University of Milan, Milan, Italy
| | - Antonio L Bartorelli
- Centro Cardiologico Monzino, IRCCS, University School of Milan, Via C. Parea, 4, 20138 Milan, Italy.,Department of Biomedical and Clinical Sciences, "Luigi Sacco", Via G.B. Grassi, 74 - 20157, University of Milan, Milan, Italy
| |
Collapse
|
4
|
Zhang X, Su Z, Yang Y, Ge L, Li B. Congenital Descending Aorta-Right Atrial Tunnel: A Case Report. Front Pediatr 2020; 8:524. [PMID: 33014928 PMCID: PMC7506122 DOI: 10.3389/fped.2020.00524] [Citation(s) in RCA: 1] [Impact Index Per Article: 0.2] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 04/19/2020] [Accepted: 07/24/2020] [Indexed: 11/16/2022] Open
Abstract
Introduction: Congenital descending aorta-right atrial tunnel is a rare congenital heart defect. Herein, a new case successfully treated by transcatheter closure using a new type of ventricular septal defect occluder from the aortic side was reported. Case Presentation: An 11-month-old Chinese girl presenting with a cardiac murmur was suspected with partial anomalous pulmonary venous connection as assessed by echocardiography. Descending aorta-right atrial tunnel was confirmed by computed tomography angiography and cardiac catheterization. Subsequently, transcatheter closure was performed successfully using a new type of ventricular septal defect occluder from the aortic side. The cardiac murmur disappeared after the intervention, and echocardiography did not reveal any abnormal flow inside the right atrium. At 6 months, the patient had no murmur, and no residual shunt was found using the echocardiogram. Conclusion: Descending aorta-right atrial tunnel is a rare anomaly. Transcatheter closure was successful in our case. Long-term follow-up is needed to assess any progressive growth of the residual tunnel.
Collapse
Affiliation(s)
- Xing Zhang
- Department of Cardiology, Kunming Children's Hospital, Kunming, China
| | - Zhongjian Su
- Department of Cardiology, Kunming Children's Hospital, Kunming, China
| | - Yanfei Yang
- Department of Cardiology, Kunming Children's Hospital, Kunming, China
| | - Liping Ge
- Department of Cardiology, Kunming Children's Hospital, Kunming, China
| | - Bin Li
- Department of Cardiology, Kunming Children's Hospital, Kunming, China
| |
Collapse
|
5
|
Castaño O, Bastidas O, Ocampo-Chaparro JM, Urrea-Zapata JK, Bucheli V. Fístula aorto-atrial derecha: una presentación inusual. REVISTA COLOMBIANA DE CARDIOLOGÍA 2018. [DOI: 10.1016/j.rccar.2018.02.002] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 11/28/2022] Open
|
6
|
Alkan F, Pabuşcu Y, Çetin M, Coşkun Ş. Successful treatment of abdominal aorto-right atrial fistula by vascular plug: A previously unreported cardiac malformation. Anatol J Cardiol 2017; 18:433-435. [PMID: 29256880 PMCID: PMC6282886 DOI: 10.14744/anatoljcardiol.2017.7973] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [MESH Headings] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 11/21/2022] Open
Affiliation(s)
- Fatoş Alkan
- Department of Pediatric Cardiology, Faculty of Medicine, Celal Bayar University, Manisa-Turkey.
| | | | | | | |
Collapse
|
7
|
Fernando RJ, Johnson SD, Augoustides JG, Patel PA, Gutsche JT, Dashiell JM, Feinman JW, Zhou E, Weiss SJ, Goldhammer JE, Panikkath PV, Gerstein NS. Simultaneous Right-Sided and Left-Sided Infective Endocarditis: Management Challenges in a Multidisciplinary Setting. J Cardiothorac Vasc Anesth 2017; 32:1041-1049. [PMID: 29249580 DOI: 10.1053/j.jvca.2017.07.031] [Citation(s) in RCA: 2] [Impact Index Per Article: 0.3] [Reference Citation Analysis] [Key Words] [Track Full Text] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 07/21/2017] [Indexed: 02/08/2023]
Affiliation(s)
- Rohesh J Fernando
- Cardiothoracic Section, Department of Anesthesiology, Wake Forest University School of Medicine, Winston Salem, NC
| | - Sean D Johnson
- Cardiothoracic Section, Department of Anesthesiology, Wake Forest University School of Medicine, Winston Salem, NC
| | - John G Augoustides
- Cardiovascular and Thoracic Section, Department of Anesthesiology and Critical Care, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
| | - Prakash A Patel
- Cardiovascular and Thoracic Section, Department of Anesthesiology and Critical Care, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA
| | - Jacob T Gutsche
- Cardiovascular and Thoracic Section, Department of Anesthesiology and Critical Care, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA
| | - Jillian M Dashiell
- Cardiovascular and Thoracic Section, Department of Anesthesiology and Critical Care, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA
| | - Jared W Feinman
- Cardiovascular and Thoracic Section, Department of Anesthesiology and Critical Care, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA
| | - Elizabeth Zhou
- Cardiovascular and Thoracic Section, Department of Anesthesiology and Critical Care, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA
| | - Stuart J Weiss
- Cardiovascular and Thoracic Section, Department of Anesthesiology and Critical Care, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA
| | - Jordan E Goldhammer
- Adult Cardiothoracic Anesthesiology, Department of Anesthesiology, Sidney Kimmel Medical College at Thomas Jefferson University Hospital, Philadelphia, PA
| | - Pramod V Panikkath
- Division of Cardiac Anesthesia, Department of Anesthesiology, University of New Mexico, Albuquerque, NM
| | - Neal S Gerstein
- Division of Cardiac Anesthesia, Department of Anesthesiology, University of New Mexico, Albuquerque, NM
| |
Collapse
|
8
|
Ho AB, Magee AG, Hayes N. Descending aorta to right atrial fistula. Catheter Cardiovasc Interv 2017; 90:1158-1160. [PMID: 28557188 DOI: 10.1002/ccd.27129] [Citation(s) in RCA: 3] [Impact Index Per Article: 0.4] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 02/24/2017] [Revised: 04/14/2017] [Accepted: 04/23/2017] [Indexed: 11/12/2022]
Abstract
Here, we report a four-day old neonate presenting with cardiovascular collapse secondary to a descending aorta to right atrial fistula. Echocardiography was suggestive of the diagnosis and confirmed with computed tomographic (CT) imaging. The fistula was successfully occluded via cardiac catheterization using an Amplatzer Vascular Plug II implanted from the right atrial aspect. This report includes the first CT imaging of this extremely rare congenital defect as well as detailing the first successful transcatheter occlusion of this particular lesion.
Collapse
Affiliation(s)
- Andrew B Ho
- Department of Paediatric Cardiology, Southampton General Hospital, Southampton, United Kingdom
| | - Alan G Magee
- Department of Paediatric Cardiology, Southampton General Hospital, Southampton, United Kingdom
| | - Nicholas Hayes
- Department of Paediatric Cardiology, Southampton General Hospital, Southampton, United Kingdom
| |
Collapse
|
9
|
Incidentally detected aorto-right atrial fistula in asymptomatic patient with operated aortic dissection. INTERNATIONAL JOURNAL OF THE CARDIOVASCULAR ACADEMY 2017. [DOI: 10.1016/j.ijcac.2016.12.002] [Citation(s) in RCA: 2] [Impact Index Per Article: 0.3] [Reference Citation Analysis] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 11/18/2022] Open
|
10
|
Said SAM, Mariani MA. Acquired aortocameral fistula occurring late after infective endocarditis: An emblematic case and review of 38 reported cases. World J Cardiol 2016; 8:488-495. [PMID: 27621777 PMCID: PMC4997530 DOI: 10.4330/wjc.v8.i8.488] [Citation(s) in RCA: 5] [Impact Index Per Article: 0.6] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Download PDF] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 02/13/2016] [Revised: 04/23/2016] [Accepted: 06/29/2016] [Indexed: 02/06/2023] Open
Abstract
AIM To delineate the features and current therapeutic option of congenital and acquired aortocameral fistulas (ACF) secondary to iatrogenic or infectious disorders.
METHODS From a PubMed search using the term "aortocameral fistula", 30 suitable papers for the current review were retrieved. Reviews, case series and case reports published in English were considered. Abstracts and reports from scientific meetings were not included. A total of 38 reviewed subjects were collected and analyzed. In addition, another case - an adult male who presented with ACF between commissures of the right and non-coronary sinuses and right atrium as a late complication of Staphylococcus aureus infective endocarditis of the AV - is added, the world literature is briefly reviewed.
RESULTS A total of thirty-eight subjects producing 39 fistulas were reviewed, analyzed and stratified into either congenital (47%) or acquired (53%) according to their etiology. Of all subjects, 11% were asymptomatic and 89% were symptomatic with dyspnea (21 ×) as the most common presentation. Diagnosis was established by a multidiagnostic approach in 23 (60%), single method in 14 (37%) (echocardiography in 12 and catheterization in 2), and at autopsy in 2 (3%) of the subjects. Treatment options included percutaneous transcatheter closure in 12 (30%) with the deployment of the Amplatzer duct or septal occluder and Gianturco coil and surgical correction in 24 (63%).
CONCLUSION Acquired ACF is an infrequent entity which may occur late after an episode of endocarditis of the native AV. The management of ACF is generally by surgical correction but non-surgical device intervention has recently been introduced as a safe alternative.
Collapse
|
11
|
Dhingra S, Husain SM, Yadav R. Coronary cameral fistula from the sinoatrial nodal artery to the right atrium. Indian J Thorac Cardiovasc Surg 2015. [DOI: 10.1007/s12055-015-0394-1] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 11/28/2022] Open
|
12
|
Habeeb K, Stankewicz H, Axelband J, Melanson S. The infected heart: ventriculoseptal abscess and intracardiac fistulization. Am J Emerg Med 2015. [PMID: 26212894 DOI: 10.1016/j.ajem.2015.06.053] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 10/23/2022] Open
Abstract
Infective endocarditis is a rare but potentially deadly infection of the endocardial layer, which can involve the valves of the heart among other structures. The extraordinarily rare complication seen in this case involves extensive damage manifesting in an aortic root abscess resulting in an abnormal communication between the aorta and the atrium known as an aortocavitary fistula (Eur Heart J 2005;26:288-297; Pediatr Cardiol 2011;32:1057-1059; J Am Coll Cardiol 1991;18:663-667). As the disease progresses, wading through the complex symptoms, which may seem unrelated, represents a key challenge in diagnosis. This case describes both early and late findings of endocarditis and highlights a rare complication in which rapid diagnosis and early surgical intervention before the development of hemodynamic sequelae are paramount. In this case, infective endocarditis, a great masquerader in this case, provided a challenging diagnostic situation, a very rare complication, and commonalities of disease characteristics that health care provider should appreciate.
Collapse
Affiliation(s)
- Keith Habeeb
- St Luke's University Hospital, Bethlehem, PA 18018.
| | | | | | | |
Collapse
|
13
|
John ES, Boyer J, Ledzian B, Steward H, Moro R, Bittner HB. A rare case of sinus of valsalva-right atrial fistula secondary to an abscess perforation from underlying aortic valve endocarditis. J Cardiothorac Surg 2014; 9:124. [PMID: 25022608 PMCID: PMC4105866 DOI: 10.1186/1749-8090-9-124] [Citation(s) in RCA: 9] [Impact Index Per Article: 0.8] [Reference Citation Analysis] [Abstract] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 12/24/2013] [Accepted: 06/27/2014] [Indexed: 11/12/2022] Open
Abstract
Sinus of Valsalva-right atrial fistulas are abnormal connections between the aorta and the right atrium, and present challenging surgical conditions. An extremely rare etiology of aorto-right atrial fistula is infective endocarditis. This case report presents a 21 year old Caucasian female patient who had native aortic valve Staphylococcus aureus endocarditis complicated by sinus of Valsalva abscess perforation associated with an acute heart block, an aorto-right atrial fistula, severe heart failure, and cardiogenic shock. She underwent emergent aortic valve replacement and complex sinus of Valsalva fistula pericardial patch reconstruction and repair. This case report further explores the advantages and disadvantages of different valves for different patient populations, and evaluates the patient’s prosthesis mismatch and effective orifice area.
Collapse
Affiliation(s)
- Elizabeth S John
- University of Central Florida, College of Medicine, Orlando, FL, USA.
| | | | | | | | | | | |
Collapse
|
14
|
Ghandour A, Rajiah P. Unusual fistulas and connections in the cardiovascular system: A pictorial review. World J Radiol 2014; 6:169-176. [PMID: 24876921 PMCID: PMC4037543 DOI: 10.4329/wjr.v6.i5.169] [Citation(s) in RCA: 12] [Impact Index Per Article: 1.1] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Download PDF] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 01/03/2014] [Revised: 02/11/2014] [Accepted: 03/14/2014] [Indexed: 02/06/2023] Open
Abstract
A fistula is an abnormal vascular connection leading to diversion of blood from a high resistance arterial circuit to low resistance venous circuit. Coronary artery fistulas are abnormal communications of the coronary artery with a chamber of the heart, or with any segment of systemic or pulmonary circulation, bypassing the myocardial capillaries. Other unusual fistulas include connection between aorta and the right atrium/superior vena cava, aorta and the inferior vena cava or between a coronary artery bypass graft and a cardiac vein. Abnormal connections also include origin of the coronary artery from the pulmonary artery. In this article, we review the imaging, particularly computed tomography and magnetic resonance imaging of unusual fistulas and connections involving the cardiovascular system, particularly the coronary arteries and the aorta.
Collapse
|
15
|
Transcatheter closure of tortuous aorto-right atrial fistula. Cardiovasc Interv Ther 2014; 30:151-4. [PMID: 24740464 DOI: 10.1007/s12928-014-0264-6] [Citation(s) in RCA: 2] [Impact Index Per Article: 0.2] [Reference Citation Analysis] [Abstract] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 01/03/2014] [Accepted: 03/30/2014] [Indexed: 10/25/2022]
Abstract
Congenital fistula between the aorta and right atrium is a rare congenital anomaly of the heart. We report a new case of this unusual communication, which was successfully closed by transcatheter embolisation using an Amplatzer duct occluder II. A 7-year-old asymptomatic girl was referred to our institute for evaluation of a murmur. Echocardiography revealed intact septae and the right coronary sinus was dilated with a fistulous tract arising from the sinus and opening into the right atrium with continuous flow into the right atrium. Computerized tomography confirmed the diagnosis and delineated the anatomy. Cardiac catheterization performed confirmed the presence of a markedly tortuous and dilated aorto-right atrial fistula. Coronary angiography demonstrated normal coronary arteries arising from the respective sinuses. The fistula was closed antegradely using an Amplatzer duct occluder II (AGA Medical Corporation, Plymouth, MN, USA). The continuous murmur had disappeared after the procedure and an echocardiogram revealed no continuous flow across the fistulous tract. The patient remained well at follow-up 3 months later.
Collapse
|
16
|
Ruptured sinus of valsalva aneurysm and coarctation of aorta in a woman at early postpartum period. Case Rep Med 2014; 2014:731596. [PMID: 24715919 PMCID: PMC3970367 DOI: 10.1155/2014/731596] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 11/04/2013] [Accepted: 02/06/2014] [Indexed: 11/22/2022] Open
Abstract
Coarctation of aorta and sinus of Valsalva aneurysm are frequently missed congenital cardiac defects that their diagnosis might be delayed. To our knowledge, coincidence of these cardiac defects is unusual and has not been reported in the literature before. Here, we present a patient with coarctation of aorta and ruptured noncoronary sinus of Valsalva aneurysm leading to aorto-right atrial fistula in the early postpartum period and our management of this unusual case.
Collapse
|
17
|
Bouchez S, Wouters PF, Vandenplas G. Asymptomatic aorto-atrial fistula identified with intraoperative transesophageal echocardiography. J Cardiothorac Vasc Anesth 2012; 26:e76-7. [PMID: 22885119 DOI: 10.1053/j.jvca.2012.06.028] [Citation(s) in RCA: 5] [Impact Index Per Article: 0.4] [Reference Citation Analysis] [Track Full Text] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 05/20/2012] [Indexed: 12/26/2022]
|