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Demonstration of the artery of Adamkiewicz at multi- detector row helical CT

Kei Takase1, Yoshihiro Sawamura, Kazumasa Igarashi

  • 1Department of Radiology, Ishinomaki Redcross Hospital, 1-7-10 Yoshino, Ishinomaki, Miyagi 986-8522, Japan. kytakase@mb.infoweb.ne.jp

Radiology
|April 4, 2002
PubMed

Insights

Multi-detector row helical computed tomography (CT) effectively visualizes the artery of Adamkiewicz in most patients. This imaging technique aids in identifying the artery

Area of Science:

  • Vascular imaging
  • Spinal artery anatomy
  • Computed tomography applications

Background:

  • The artery of Adamkiewicz is crucial for spinal cord vascularization.
  • Accurate depiction of this artery is vital for surgical planning and understanding spinal pathologies.
  • Limited visualization of the artery of Adamkiewicz can pose challenges in clinical practice.

Purpose of the Study:

  • To evaluate the efficacy of multi-detector row helical CT in visualizing the artery of Adamkiewicz.
  • To assess the detailed anatomical characteristics of the artery of Adamkiewicz using this imaging modality.

Main Methods:

  • Seventy patients with vascular diseases underwent multi-detector row helical CT of the aorta and iliac arteries.
  • The artery of Adamkiewicz was analyzed using multiplanar, curved planar reformations, and cine-mode displays.
  • Key parameters investigated included visualization, origin side, and vertebral level of the artery.

Main Results:

  • The artery of Adamkiewicz was clearly visualized in 90% of patients.
  • Left-sided origin (71%) and thoracic/lumbar levels (T8-L1, 92%) were most common.
  • Full-length continuity from the spinal artery was traceable in 32% of visualized cases.

Conclusions:

  • Multi-detector row helical CT is a highly effective method for depicting the artery of Adamkiewicz.
  • This technique provides valuable anatomical information regarding the artery's origin and course.
  • High visualization rates suggest its utility in clinical scenarios requiring assessment of spinal vascular supply.
Abstract

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