{"title":"利用多层螺旋CT血管造影研究双进气道左心室患者的心血管形态及相关异常。","authors":"Niraj Nirmal Pandey, Mansi Verma, Sheetal Sharma, Damandeep Singh, Vineeta Ojha, Sanjeev Kumar, Sivasubramanian Ramakrishnan, Priya Jagia","doi":"10.1007/s00246-025-04053-7","DOIUrl":null,"url":null,"abstract":"<p><p>The present study sought to evaluate the intracardiac morphology and associated cardiovascular anomalies in patients with double inlet left ventricle (DILV) on multidetector CT angiography. A retrospective search of the electronic departmental database was conducted from January 2014 to January 2023 to identify patients with a diagnosis of DILV on cardiac CT angiography. Patients with a common atrioventricular valve were excluded. The scans were systematically reviewed in a sequential segmental fashion for evaluating the intracardiac morphology and associated cardiovascular abnormalities. DILV was identified in 97 patients (74 males; mean age: 5.15 years). A hypoplastic right ventricular cavity was seen in all patients. The most prevalent ventriculo-arterial configuration was transposition of great arteries seen in 60/97 (61.9%) patients. Concordant ventriculo-arterial connections (Holmes heart) were observed in 17/97 (17.5%) patients while double outlet right ventricle and origin of aorta from right ventricle with pulmonary atresia were seen in 8/97 (8.2%) patients respectively. Aortic arch anomalies were seen in 11/97 (11.3%) patients. Type A interrupted aortic arch was present in 1 (1%) patient, and 2 (2.1%) patients had aortic stenosis. Some form of pulmonary outflow obstruction was seen in 45/97 (46.4%). Pulmonary atresia was observed in 11/97 (11.3%) patients out of which 1 had non-confluent pulmonary arteries. Pulmonary venous anomalies were observed in 4/97 (4.1%) patients. A single coronary artery was seen in 6/97 (6.2%) patients. DILV is a congenital heart disease with functionally single ventricle and is associated with a wide variety of cardiovascular anomalies, most commonly transposition of great arteries and pulmonary outflow tract obstruction. Multidetector CT angiography is an excellent modality for detailed intracardiac anatomical evaluation and depiction of associated cardiovascular anomalies which may aid in deciding the surgical approach.</p>","PeriodicalId":19814,"journal":{"name":"Pediatric Cardiology","volume":" ","pages":""},"PeriodicalIF":1.4000,"publicationDate":"2025-10-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Clarifying the Cardiovascular Morphology and Associated Abnormalities in Patients with Double Inlet Left Ventricle Using Multidetector CT Angiography.\",\"authors\":\"Niraj Nirmal Pandey, Mansi Verma, Sheetal Sharma, Damandeep Singh, Vineeta Ojha, Sanjeev Kumar, Sivasubramanian Ramakrishnan, Priya Jagia\",\"doi\":\"10.1007/s00246-025-04053-7\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The present study sought to evaluate the intracardiac morphology and associated cardiovascular anomalies in patients with double inlet left ventricle (DILV) on multidetector CT angiography. A retrospective search of the electronic departmental database was conducted from January 2014 to January 2023 to identify patients with a diagnosis of DILV on cardiac CT angiography. Patients with a common atrioventricular valve were excluded. The scans were systematically reviewed in a sequential segmental fashion for evaluating the intracardiac morphology and associated cardiovascular abnormalities. DILV was identified in 97 patients (74 males; mean age: 5.15 years). A hypoplastic right ventricular cavity was seen in all patients. The most prevalent ventriculo-arterial configuration was transposition of great arteries seen in 60/97 (61.9%) patients. Concordant ventriculo-arterial connections (Holmes heart) were observed in 17/97 (17.5%) patients while double outlet right ventricle and origin of aorta from right ventricle with pulmonary atresia were seen in 8/97 (8.2%) patients respectively. Aortic arch anomalies were seen in 11/97 (11.3%) patients. Type A interrupted aortic arch was present in 1 (1%) patient, and 2 (2.1%) patients had aortic stenosis. Some form of pulmonary outflow obstruction was seen in 45/97 (46.4%). Pulmonary atresia was observed in 11/97 (11.3%) patients out of which 1 had non-confluent pulmonary arteries. Pulmonary venous anomalies were observed in 4/97 (4.1%) patients. A single coronary artery was seen in 6/97 (6.2%) patients. DILV is a congenital heart disease with functionally single ventricle and is associated with a wide variety of cardiovascular anomalies, most commonly transposition of great arteries and pulmonary outflow tract obstruction. Multidetector CT angiography is an excellent modality for detailed intracardiac anatomical evaluation and depiction of associated cardiovascular anomalies which may aid in deciding the surgical approach.</p>\",\"PeriodicalId\":19814,\"journal\":{\"name\":\"Pediatric Cardiology\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":1.4000,\"publicationDate\":\"2025-10-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Pediatric Cardiology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1007/s00246-025-04053-7\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CARDIAC & CARDIOVASCULAR SYSTEMS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pediatric Cardiology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s00246-025-04053-7","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CARDIAC & CARDIOVASCULAR SYSTEMS","Score":null,"Total":0}
Clarifying the Cardiovascular Morphology and Associated Abnormalities in Patients with Double Inlet Left Ventricle Using Multidetector CT Angiography.
The present study sought to evaluate the intracardiac morphology and associated cardiovascular anomalies in patients with double inlet left ventricle (DILV) on multidetector CT angiography. A retrospective search of the electronic departmental database was conducted from January 2014 to January 2023 to identify patients with a diagnosis of DILV on cardiac CT angiography. Patients with a common atrioventricular valve were excluded. The scans were systematically reviewed in a sequential segmental fashion for evaluating the intracardiac morphology and associated cardiovascular abnormalities. DILV was identified in 97 patients (74 males; mean age: 5.15 years). A hypoplastic right ventricular cavity was seen in all patients. The most prevalent ventriculo-arterial configuration was transposition of great arteries seen in 60/97 (61.9%) patients. Concordant ventriculo-arterial connections (Holmes heart) were observed in 17/97 (17.5%) patients while double outlet right ventricle and origin of aorta from right ventricle with pulmonary atresia were seen in 8/97 (8.2%) patients respectively. Aortic arch anomalies were seen in 11/97 (11.3%) patients. Type A interrupted aortic arch was present in 1 (1%) patient, and 2 (2.1%) patients had aortic stenosis. Some form of pulmonary outflow obstruction was seen in 45/97 (46.4%). Pulmonary atresia was observed in 11/97 (11.3%) patients out of which 1 had non-confluent pulmonary arteries. Pulmonary venous anomalies were observed in 4/97 (4.1%) patients. A single coronary artery was seen in 6/97 (6.2%) patients. DILV is a congenital heart disease with functionally single ventricle and is associated with a wide variety of cardiovascular anomalies, most commonly transposition of great arteries and pulmonary outflow tract obstruction. Multidetector CT angiography is an excellent modality for detailed intracardiac anatomical evaluation and depiction of associated cardiovascular anomalies which may aid in deciding the surgical approach.
期刊介绍:
The editor of Pediatric Cardiology welcomes original manuscripts concerning all aspects of heart disease in infants, children, and adolescents, including embryology and anatomy, physiology and pharmacology, biochemistry, pathology, genetics, radiology, clinical aspects, investigative cardiology, electrophysiology and echocardiography, and cardiac surgery. Articles which may include original articles, review articles, letters to the editor etc., must be written in English and must be submitted solely to Pediatric Cardiology.