論文

査読有り
2017年10月

Congenital anomalies of the left brachiocephalic vein detected in adults on computed tomography

JAPANESE JOURNAL OF RADIOLOGY
  • Hiroshi Yamamuro
  • ,
  • Tamaki Ichikawa
  • ,
  • Jun Hashimoto
  • ,
  • Shun Ono
  • ,
  • Yoshimi Nagata
  • ,
  • Shuichi Kawada
  • ,
  • Makiko Kobayashi
  • ,
  • Jun Koizumi
  • ,
  • Takeo Shibata
  • ,
  • Yutaka Imai

35
10
開始ページ
597
終了ページ
605
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1007/s11604-017-0673-4
出版者・発行元
SPRINGER

Anomalous left brachiocephalic vein (BCV) is a rare and less known systemic venous anomaly. We evaluated congenital anomalies of the left BCV in adults detected during computed tomography (CT) examinations.
This retrospective study included 81,425 patients without congenital heart disease who underwent chest CT. We reviewed the recorded reports and CT images for congenital anomalies of the left BCV including aberrant and supernumerary BCVs. The associated congenital aortic anomalies were assessed.
Among 73,407 cases at a university hospital, 22 (16 males, 6 females; mean age, 59 years) with aberrant left BCVs were found using keyword research on recorded reports (0.03%). Among 8018 cases at the branch hospital, 5 (4 males, 1 female; mean age, 67 years) with aberrant left BCVs were found using CT image review (0.062%). There were no significant differences in incidences of aberrant left BCV between the two groups. Two cases had double left BCVs. Eleven cases showed high aortic arches. Two cases had the right aortic arch, one case had an incomplete double aortic arch, and one case was associated with coarctation.
Aberrant left BCV on CT examination in adults was extremely rare. Some cases were associated with aortic arch anomalies.

リンク情報
DOI
https://doi.org/10.1007/s11604-017-0673-4
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/28849388
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000412679800007&DestApp=WOS_CPL
ID情報
  • DOI : 10.1007/s11604-017-0673-4
  • ISSN : 1867-1071
  • eISSN : 1867-108X
  • PubMed ID : 28849388
  • Web of Science ID : WOS:000412679800007

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