Document Detail


Anomalous subaortic left brachiocephalic vein in surgical cases and literature review.
MedLine Citation:
PMID:  20830788     Owner:  NLM     Status:  In-Process    
Abstract/OtherAbstract:
Anomalous subaortic left brachiocephalic vein (ASLBV) is a rare systemic venous anomaly. We review our experience with patients associated with ASLBV who underwent cardiac surgery at three institutions. From 1989 to 2009, the medical records of surgically treated patients with ASLBV were analyzed; the incidence of ASLBV, clinical characteristics, and associated anatomical findings were assessed. Fifteen patients had ASLBV. All ASLBVs coursed left lateral to the aortic arch, passed under the ascending aorta anterior to the central pulmonary artery, and joined the right brachiocephalic vein. Fourteen patients had congenital heart disease (CHD), and the remaining patient did not have cardiac anomalies. Its incidence was 0.57% (14 of 2,449) in patients with CHD and only 0.02% (1 of 4,805) in patients without CHD. In patients with CHD, 73.3% (11 of 15) of the patients had conotruncal cardiac anomalies such as tetralogy of Fallot, ventricular septal defect with pulmonary atresia, truncus arteriosus, and interruption of the aortic arch. Eight patients had aortic arch anomalies, including right aortic arch and cervical aortic arch. The deletion of chromosomal 22q11.2 was confirmed in two patients, and one patient was diagnosed with DiGeorge syndrome. ASLBV was clinically silent even without any surgical intervention. ASLBV is a very rare anomaly and is highly associated with conotruncal cardiac anomalies and aortic arch anomalies, including right aortic arch and cervical aortic arch. Preoperative diagnosis is important when any surgical interventions are intended, especially, in patients with conotruncal cardiac anomalies.
Authors:
Mitsugi Nagashima; Fumiaki Shikata; Toru Okamura; Eiichi Yamamoto; Takashi Higaki; Masashi Kawamura; Masahiro Ryugo; Hironori Izutani; Hiroshi Imagawa; Shunji Uchita; Yoshitaka Okamura; Hiroyuki Suzuki; Yoshitsugu Nakamura; Osamu Tagusari; Kanji Kawachi
Related Documents :
14654648 - Chromosome 22q11 deletion in patients with ventricular septal defect: frequency and ass...
9972888 - Reoperation after repair of type a and b dissecting aneurysm.
16228958 - Anatomical variations in the branches of the human aortic arch: a recent study of a sou...
20345858 - Validation of the murine aortic arch as a model to study human vascular diseases.
2237958 - Giant basilar aneurysm in the course of subacute bacterial endocarditis.
18436228 - Lipocalin-type prostaglandin d synthase is a powerful biomarker for severity of stable ...
Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  Clinical anatomy (New York, N.Y.)     Volume:  23     ISSN:  1098-2353     ISO Abbreviation:  Clin Anat     Publication Date:  2010 Nov 
Date Detail:
Created Date:  2010-10-27     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  8809128     Medline TA:  Clin Anat     Country:  United States    
Other Details:
Languages:  eng     Pagination:  950-5     Citation Subset:  IM    
Affiliation:
Department of Cardiothoracic Surgery, Ehime University School of Medicine, Ehime, Japan. mitsugi@aqua.plala.or.jp
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Prediction of sustained response to peginterferon alfa-2b for hepatitis B e antigen-positive chronic...
Next Document:  P2Y13 receptor is critical for reverse cholesterol transport.