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Focal Nodular Hyperplasia of the Liver: Diffusion-Weighted Magnetic Resonance Imaging Characteristics Using High b Values

Dohan, Anthony MD; Soyer, Philippe MD, PhD; Guerrache, Youcef MD; Hoeffel, Christine MD, PhD; Gavini, Jean-Philippe MD; Kaci, Rachid MD; Boudiaf, Mourad MD

Journal of Computer Assisted Tomography: January/February 2014 - Volume 38 - Issue 1 - p 96–104
doi: 10.1097/RCT.0b013e3182a91006
Abdominal Imaging

Objective To qualitatively and quantitatively assess the presentation of hepatic focal nodular hyperplasia (FNH) at diffusion-weighted magnetic resonance imaging (DWMRI) using multiple high b values.

Materials and Methods Twenty-five patients with 27 FNHs had liver DWMRI at 1.5 T using free-breathing acquisition and 3 b values (0, 600, 1000 s/mm2). Focal nodular hyperplasias were evaluated qualitatively using visual analysis of diffusion-weighted magnetic resonance (DWMR) images and quantitatively using conventional apparent diffusion coefficient (ADC) and normalized ADC measurements.

Results All FNHs (100%) were visible on b 0 DWMR images; 26 of the 27 FNHs (96%), on b 600 DWMR images; and 21 of the 27 FNHs (78%), on b 1000 DWMR images. A total of 18 of the 27 FNHs (67%) exhibited a hyperintense central scar on the b 0 DWMR images that remained visible on the b 600 and b 1000 DWMR images in 6 of the 27 FNHs (22%). Conventional ADC value of FNHs (1.318 × 10−3 mm2/±0.208) was significantly lower than that of adjacent hepatic parenchyma (1.414 × 10−3 mm2/s ± 1.95) (P = 0.0003), although a substantial overlap was found. The use of normalized ADC using the liver as reference organ resulted in a more restricted distribution of ADC values (variation coefficient, 5.3%).

Conclusions Focal nodular hyperplasias show a wide range of morphological features at DWMRI using high b values. Further studies are needed to fully investigate as to what extent normalized ADC may result in better lesion characterization.

From the *Department of Abdominal Imaging, Hôpital Lariboisière, Assistance Publique-Hôpitaux de Paris; †Université Paris-Diderot, Sorbonne Paris Cité; ‡UMR INSERM 965-Paris 7 “Angiogenèse et recherche translationnelle”; §Department of Radiology, Hôpital Robert Debré, Reims Cedex; and ∥Department of Pathology, Hôpital Lariboisière, Assistance Publique-Hôpitaux de Paris, Paris, France.

Received for publication July 1, 2013; accepted August 12, 2013.

Reprints: Philippe Soyer, MD, PhD, Paris, France (e-mail:

The authors declare no conflict of interest.

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