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Quantitative Contrast-Enhanced Magnetic Resonance Lymphangiography of the Upper Limbs in Breast Cancer Related Lymphedema: An Exploratory Study

期刊

LYMPHATIC RESEARCH AND BIOLOGY
卷 13, 期 2, 页码 100-106

出版社

MARY ANN LIEBERT, INC
DOI: 10.1089/lrb.2014.0039

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资金

  1. CR-UK Cancer Imaging Centre [C1060/A16464]
  2. NIHR/HEE Healthcare Science Doctoral Research Fellowship from National Institute for Health Research
  3. Health Education England
  4. British Heart Foundation [FS/11/40/28739]
  5. British Heart Foundation [PG/10/58/28477, FS/11/40/28739] Funding Source: researchfish
  6. Cancer Research UK [16464] Funding Source: researchfish
  7. National Institute for Health Research [NF-SI-0512-10162, NIHR-HCS-D13-04-002] Funding Source: researchfish
  8. National Institutes of Health Research (NIHR) [NIHR-HCS-D13-04-002] Funding Source: National Institutes of Health Research (NIHR)

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Background: Contrast-Enhanced Magnetic Resonance Lymphangiography (CE-MRL) presents some limitations: (i) it does not quantify lymphatic functionality; and (ii) enhancement of vascular structures may confound image interpretation. Furthermore, although CE-MRL is well described in the published literature for the lower limbs, there is a paucity of data with regards to its use in the upper limbs. In this proof-of-principle study, we propose a new protocol to perform CE-MRL in the upper limbs of patients with breast cancer-related lymphedema (BCRL) which addresses these limitations. Methods and Results: CE-MRL was performed using a previously published (morphological) protocol and the proposed protocol (quantitative) on both the ipsilateral (abnormal) and contralateral (normal) arms of patients with BCRL. The quantitative protocol employs contrast agent (CA) intradermal injections at a lower concentration to prevent T2*-related signal decay. Both protocols provided high-resolution three-dimensional images of upper limb lymphatic vessels. CA uptake curves were utilized to distinguish between lymphatic vessels and vascular structures. The quantitative protocol minimized venous enhancement and avoided spurious delays in lymphatic enhancement due to short T2* values, enabling correct CA uptake characterization. The quantitative protocol was therefore employed to measure the lymphatic fluid velocity, which demonstrated functional differences between abnormal and normal arms. The velocity values were in agreement with previously reported lymphoscintigraphy and near infra-red lymphangiography measurements. Conclusions: This work demonstrated the feasibility of CE-MRL of the upper limbs in patients with BRCL, introducing an advanced imaging and analysis protocol suitable for anatomical and functional study of the lymphatic system.

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