Objectives: The purpose of this study was to retrospectively compare color Doppler Ultrasonography (CD-US) and diffusion weighted Magnetic Resonance Enterography (DWI-MRE) in the evaluation of disease severity of pediatric inflammatory bowel diseases (IBD). Materials and methods: During the period between February 2010 and November 2012, 36 patients affected by IBD, aged between 7.8 and 18.5 years (mean 11.9 years) underwent, in the same week, CD-US, DWI-MRE [completed by apparent diffusion coefficient (ADC) calculation] and ileocolonoscopy with intestinal biopsies. Overall, 53 bowel segments (27 ileal, 26 colonic) were examined. At CD-US evaluation, a wall thickness > 3 mm in the small bowel and >2 mm in the large bowel, associated with an increased intramural vascularity, were considered abnormal. ADC values were significant when lower than 2 × 10
﹣3
mm
2
/sec. Histopathological grading of inflammation distinguished between active (mild, moderate and severe) and inactive disease. For each segment, CD-US findings and ADC values were compared with histology. Results: CD-US correctly graded 46/53 cases (86.8%) as compared with histology. Statistical analysis demonstrated a negative correlation between ADC and histology, with the results corresponding in 43/53 cases (81.1%). Conclusions: Our study shows that both CD-US and DWI-MRE are non-invasive, useful diagnostic tools for the grading of IBD activity in children.
Inflammatory bowel diseases (IBD) are chronic, complex, multifactorial disorders which develop in genetically predisposed subjects [1] : they include Crohn’s disease (CD), ulcerative colitis (UC) and indeterminate colitis (IC) [2] [3] . Several studies have reported that they are constantly on the increase [4] [5] : the prevalence of UC is 505 per 100,000 people in Europe and 249 per 100,000 in North America and of CD, 322 per 100,000 people in Europe and 319 per 100,000 in North America. Children and adolescents (aged between 0 and 18 years) account for about 25% - 30% of the affected population [6] . The potential to cause lifelong ill health has an extremely high impact on the patient, their family or other carers and society [7] . Therefore, an early diagnosis and adequate follow-up timing are crucial, because they allow a proper management plan and therapy to be scheduled, avoiding unnecessary examinations [8] .
Endoscopic and histological evaluation is the gold standard for the diagnosis and the grading of IBD, but it has some limitations [9] : it is an invasive procedure and it is often poorly tolerated, especially by the youngest patients. Moreover, it can be non-diagnostic in cases of significant stenosis.
Imaging modality plays a fundamental role in the diagnosis: it includes traditional radiology, ultrasonography (US), computerized tomography (CT) and magnetic resonance enterography (MRE).
Particularly, cross-sectional techniques (US, CT and MRE) have advanced the ability to diagnose, classify and monitor IBD [10] ; their employment has radically modified the diagnostic approach coupling the study of the mucosal surface with a direct evaluation of wall thickening and extraluminal lesions.
Medical imaging in childhood must take into account the problem of dosimetry and radioprotection. This concept is strongly endorsed by the Society for Pediatric Radiology, particularly in the use of procedures and modalities involving higher radiation doses. Current imaging methods must be optimized for radiation dose reduction in pediatric patients who might be as much as ten times more radiosensitive than adults [11] .
The use of trans-abdominal ultrasound for the assessment of patients with IBD is gaining popularity. The lack of ionizing radiation is particularly attractive when examining young patients undergoing frequent follow-up. However, even if US is widely available and relatively inexpensive [12] , operator dependability and experience in the use for bowel assessment still pose major limitations [13] .
MR is increasingly being used. Recent studies have assessed its ability to diagnose, to quantify disease extent, to detect inflammation or to show complications such as stenosis or fistula [14] . Its application is justified by the absence of ionizing radiation, along with very high soft-tissue contrast, multiplanar images, a low incidence of adverse events related to the use of intravenous contrast medium, and high diagnostic accuracy in the evaluation of luminal and extraluminal abnormalities [15] .
Diffusion-weighted magnetic resonance (DWI-MR) imaging is a technique that relies on the diffusion of water in biologic tissues to produce images providing functional, quantitative information about tissue cellularity. The images are produced on the basis of the random (Brownian) motion of water molecules suspended in a liquid: each pixel is a representation of the average diffusion of water in the volume imaged [16] . Until now, no threshold of apparent diffusion coefficient (ADC), the quantitative parameter of DWI, has been established for defining inflammation in IBD [14] .
At present, there is no single imaging modality that has been proven universally superior in either suspected or established IBD [17] . An important matter of concern, particularly in younger patients, is ionizing radiation exposure as a potential risk factor for cancer, especially considering that the risk of malignancies is increased in these patients due not only to the disease but also to treatments [18] .
The aim of our study was to compare two non-ionizing techniques, namely color Doppler ultrasonography (CD-US) and diffusion weighted magnetic resonance enterography (DWI-MRE) with quantitative analysis of the ADC value, in the evaluation of the grade of activity in pediatric IBD, considering histology as the reference standard. To our knowledge, this study is the first to compare CD-US and ADC measurement for the definition of disease activity in pediatric IBD.
2. Materials and Methods2.1. Patients
During the period between February 2010 and November 2012, 94 children and young adults (aged between 2.8 and 18.3 years, mean 11 years, median 13.15 years) underwent a pediatric gastroenterologic evaluation for suspected, non-diagnosed IBD or during follow-up for diagnosed IBD: CD-US and MRE were performed on this occasion in all the cases.
Among this group, we retrospectively selected all those subjects who had undergone, during the same week, CD-US, DWI-MRE with ADC calculation and intestinal biopsy: 36 patients met our inclusion criteria.
We excluded all patients aged more than 19 years, those who had not undergone one examination among US, MRE and histology, and those who did not undergo all three examinations during the same week.
The final sample consisted of 16 females (44.4%) and 20 males (55.6%), aged between 7.8 and 18.5 years (mean 11.9, median 12.9 years). Of these, 15 of 36 patients (41.7%) were examined for suspected IBD, while 21 (58.3%) had histological confirmation of the disease and were undergoing follow-up. Therefore, from 36 patients, 27 were affected by Crohn’s disease, 4 by ulcerative colitis and 5 by indeterminate colitis. At the time of the observation, two patients had already undergone surgery and endoscopic dilatation for stricture complications.
2.2. Imaging Modalities
During the ultrasonographic and MR examination the bowel was considered in six distinct segments: terminal ileum, caecum, ascending colon, transverse colon, descending colon, sigmoid colon-rectum; overall, we examined 53 intestinal segments (27 ileal, 26 colonic).
2.3. Ultrasound Examination
Ultrasound examinations were performed by two experienced radiologists (G.A. and M.M. with 30 and 10 years of experience, respectively) blinded to the histology results, using a Philips HDI5000 SonoCT unit.
No special patient preparation was required prior to US other than a 6-h fasting without intake of solid foods and no contrast medium was used to fill the bowel.
After preliminary screening of the entire abdomen using a convex 2 - 5 MHz probe, a linear 5 - 12 MHz probe was used to study the small and large bowel loops (PRF 1000). Then the intramural vascularity was measured on color and power Doppler mode. The gain and the time gain compensation (TGC) were adjusted in order to minimize noise artifacts and to improve signal intensity. The parameters evaluated were bowel wall thickness (using a threshold of 3 mm for the terminal ileum and 2 mm for the colon) and intramural vascularity at the site of thickening. The severity of the disease was classified on the basis of the semiquantitative Limberg score, which couples wall thickening with the Doppler signal intensity. Grade 1 corresponds to a thickness greater than normal with partially obliterated wall layers but no increased vascularity. Grade 2 describes bowel wall thickening with spots of vascularity, while in grade 3 there are longer stretches of vascularity and in grade 4 the vascularized stretches extend into the mesentery [19] [20] .
2.4. MRE Protocol and Imaging Technique
MRE examination was performed using a 1.5 Tesla scan (Philips, Achieva 1.5 T), with phased array body coil (SENSE-body coil). Two experienced gastrointestinal radiologists (G.A. and M.M.), blinded to the histological findings, evaluated the images.
All the patients were asked to stop eating solid foods for 3 days before MRE to cleanse the bowel. They also took oral cleansing laxatives (Movicol Norgine Italia Srl) for variable times and personalized doses. Allergic patients received anti-allergic premedication with corticosteroids and antihistamines.
On the day of the examination the patients drank a solution of biphasic contrast medium [polyethylene glycol (PEG)], previously prepared by dissolving a granular powder in 1000 ml of water. The volume of contrast medium ranged from 200 and 1000 ml depending on the patient’s weight and was administered starting from one hour before MRE, in split doses and intervals based on the patient’s compliance. No spasmolytic medication was used to inhibit bowel peristalsis: in all the cases a good degree of distension of the bowel loops was obtained. Patients were all studied in supine position.
The imaging protocol consisted of the following breath-hold sequences, acquired without administration of contrast medium: fluoroscopic rapid acquisition with relaxation enhancement (RARE), 120 mm thick, 10 seconds acquisition time, coronal and axial balanced fast field echo (B-FFE), coronal and axial T2w single shot turbo spin echo (SSh-TSE), axial T2w single shot turbo spin echo SPAIR (SSh-TSE-SPAIR), coronal and axial T1w high-resolution isotropic volume (THRIVE). After i.v. administration of 0.15 ml/kg of gadolinium diethylene-triamine penta acetic acid (Gd-DTPA) 0.5 M followed by 20 ml of saline solution, coronal and axial T1w high-resolution isotropic volume (THRIVE) sequences were performed. DWI sequences were acquired during free breathing, before the administration of Gd-DTPA, on the axial plane, setting b 0 - 600 s/mm2, matrix 256 × 256, slice number 40, thickness 7 mm, TE 75 ms, TR 8000 ms, flip angle 90˚, FOV 350 - 450 (Table 1). DWI hyperintensity was considered abnormal and the ADC value was calculated at the same level on automatically generated ADC maps. Two small circular regions of interest (ROIs) with a diameter equivalent to the thickness of the intestinal wall were placed on each bowel segment assessed and the mean values were recorded for statistical analysis. The mean ROI area was 15/20 mm2.
2.5. Histopathological Analysis
A board-certified pathologist (S.R., with 20 years of experience in gastrointestinal pathology) performed the histological assessment on three ileal and/or colic samples per patient, obtained during ileocolonoscopy and stained with hematoxylin and eosin. Based on different grading scales for CD and UC, the disease was classified as inactive, mild, moderate or severe [21] [22] . Then, the CD-US and ADC results were compared with histological findings.
2.6. Statistical Analysis
Data on each patient, including demographic variables, CD-US results, ADC values and histological findings, were collected in a standardized form and then input into a database using File Maker Pro software and analyzed with STATA MP11 statistical software. CD-US and histological results were reported as frequency and percentage. ADC was indicated as mean value, with standard deviation (SD) and range. The agreement between CD-US and histology was calculated using Cohen’s kappa coefficient. The results of each CD-US examination were compared with the histological grade of disease: sensitivity, specificity, positive predictive value (PPV) and negative predictive value (NPV) (95% confidence interval) were calculated for each class of results. We
Magnetic resonance imaging protocol
Magnetic resonance protocol
1
Fluoroscopic rapid acquisition with relaxation enhancement (RARE) (120 mm thick, 10 seconds acquisition time)
2
Coronal and axial balanced fast field echo (B-FFE)
3
Coronal and axial T2wi single shot turbo spin echo (SSh-TSE)
4
Axial T2wi single shot turbo spin echo SPAIR (SSh-TSE-SPAIR)
5
Coronal and axial T1wi high-resolution isotropic volume (THRIVE)
6
Axial DWI sequences with b 0 - 600 s/mm2 with autogeneratedADC map
7
Coronal and axial T1wi high-resolution isotropic volume (THRIVE) after administration of 0.15 ml/kg of Gd-DTPA 0.5 M
also assessed the relation between ADC and histology using Spearman’s correlation coefficient. For each test, 95% Confidence Intervals (95% CI) were indicated. Values of p < 0.05 were considered statistically significant. Informed written consent was obtained from all the patients aged 18 years or their legal guardians if younger than 18 years, for all diagnostic and therapeutic measures. The study was approved by the local ethics committee.
3. Results
The histological findings revealed inactivity in 4 out of 53 cases, mild activity in 19 cases, moderate activity in 18 and severe activity in 12 of 53 cases (Table 2).
Results of bowel CD-US (Figure 1) showed inactive disease in 5 of the 53 cases, mild active in 15 cases, moderate active in 19 cases and severe disease in 14 of the 53 cases (Table 3).
Therefore, in 46 out of the 53 cases (86.8%) there was agreement between the ultrasonographic score and histological grading (4/4 inactivity, 15/19 mild activity, 18/18 moderate activity and 12/12 severe activity). In 5/53 cases (9.4%) CD-US overestimated the severity of the disease (mild histological activity vs moderate and severe US activity), while in 2/53 cases (3.8%) there was an underestimation (moderate histological activity vs inactivity and mild US activity).
The observed agreement between CD-US and histology was 86.8% (Table 4). Sensitivity, specificity, positive predictive value (PPV) and negative predictive value (NPV) for CD-US results, as compared to the histological classification of disease severity, are reported in Table 5.
All the abnormal intestinal segments showed hyperintense signal at DWI evaluation (Figure 2; Figure 3). The ADC values ranged from 0.17 to 1.986 × 10−3 mm2/sec. A negative correlation was found between ADC and histology (Spearman’s coefficient −0.785; p < 0.01): the higher the ADC values (>1 × 10−3 mm2/sec), the lower the disease activity (inactive or mild). On the contrary, as disease activity increased, ADC tended to decrease (<1 × 10−3 mm2/sec), as shown in Figure 4.
ADC results showed a correlation with the histological grade of activity in 43 out of 53 cases (81.1%); no association was observed in the remaining 10 (18.9%).
Assuming 1 × 10−3 mm2/sec as the cut off value between active and inactive disease, we observed that values lower than 1 × 10−3 mm2/sec corresponded to moderate-severe activity (31/37 cases, 83.8%), while values higher than 1 × 10−3 mm2/sec corresponded to inactivity or mild activity (12/16 cases, 75%).
Frequency distribution for histology results (with percentage and 95% confidence interval indication)
Histology results
N
%
Inactivity
4
7.6 (3.0 - 17.9)
Mild activity
19
35.8 (24.3 - 49.3)
Moderate activity
18
34.0 (22.7 - 47.4)
Severe activity
12
22.6 (13.4 - 35.5)
Total
53
100.0
Frequency distribution for color Doppler ultrasonography results (with percentage and 95% confidence interval indication)
Ultrasonography results
N
%
Inactivity
5
9.4 (4.1 - 20.3)
Mild activity
15
28.3 (18.0 - 41.6)
Moderate activity
19
35.9 (18.0 - 41.6)
Severe activity
14
26.4 (16.4 - 39.6)
Total
53
100.0
Color Doppler ultrasonography Limberg score. (a) Grade 1: Bowel wall thickening with partially obliterated wall layers, but no in- creased vascularity; (b) Grade 2: Bowel wall thickening with spots of vas- cularity; (c) Grade 3: Bowel wall thickening with longer stretches of vas- cularity; (d) Grade 4: Bowel wall thickening with stretches extending into the mesentery
Crohn’s disease. (a) Axial balanced fast field echo (B-FFE) sequence―marked circumferential terminal ileum bowel wall thickening; (b) Axial diffusion weighted (DWI) sequence―terminal ileum restricted diffusion with a hyperintense signal; (c) Apparent diffusion coefficient (ADC) map―the ADC value calculated at the same level was 1.326 × 10<sup>−</sup><sup>3</sup> mm<sup>2</sup>/s
Ulcerative Colitis. (a) Axial balanced fast field echo (B-FFE) sequence― Diffuse bowel wall thickening of the descending colon; (b) Axial diffusion weighted (DWI) sequence―hyperintense signal at the same level; (c) Apparent diffusion co- efficient (ADC) map―The ADC value was 0.817 × 10<sup>−</sup><sup>3</sup> mm<sup>2</sup>/s
Linear correlation between apparent diffusion coefficient ADC values and the histologic classification of disease severity
Observed, expected and Kappa agreement between histological and sonographic classification of bowel disease severity
Agreement
Expected agreement
Kappa
Std. Error
z
p
Histological vs Sonographic classification
86.8
29.0
0.81
0.09
9.56
0.00
Sensitivity, specificity, positive and negative predicted values (with 95% confidence interval indication) for Color Doppler Ultrasonography (CD-US) results associated to histological classification of disease severity
CD-US
Sensitivity
Specificity
PPV
NPV
No activity
80 (28.4 - 99.5)
100 (92.6 - 100.0)
100 (39.8 - 100.0)
98.0 (89.1 - 99.9)
Mild activity
93.3 (68.1 - 99.8)
86.8 (71.9 - 95.6)
73.7 (48.8 - 90.9)
97.1 (84.7 - 99.9)
Moderate activity
84.2 (60.4 - 96.6)
94.1 (80.3 - 99.3)
88.9 (65.3 - 98.6)
91.4 (76.9 - 98.2)
Severe activity
85.7 (57.2 - 98.2)
100.0 (91.1 - 100.0)
100.0 (73.5 - 100.0)
95.1 (83.5 - 99.4)
4. Discussion
Assessment of the disease activity is fundamental for a rational management of IBD. Recently, there has been a growing awareness of the shortcomings of only a clinical evaluation for assessment of the disease activity. Some patients with an established diagnosis of IBD and symptoms compatible with a disease flare do not have evidence of active IBD according to laboratory, endoscopic and radiologic criteria [23] .
On the other hand, the laboratory tests and radiologic evaluation of asymptomatic affected patients can sometimes reveal a relapse [24] . In a sizable proportion of cases, IBD starts in childhood and requires numerous follow-up examinations during life: therefore, specific, noninvasive, well-tolerated and repeatable imaging techniques are needed.
According to the literature, US has been widely recognized as a first line imaging modality in children [25] - [28] . The detection of an abnormal bowel wall thickening is a common US finding on which to diagnose IBD, using different thickness values as a threshold, ranging in children from 1.5 to 3 mm for the terminal ileum and from 2 to 3 mm for the colon [29] [30] , with 75/94% sensitivity and 67/100% specificity [31] . Vascular lesions and microvascular changes are well known features of IBD: in several studies, Doppler ultrasound has been found increasingly useful for the investigation of splanchnic hemodynamics and it has been demonstrated that the vascularization pattern can be used to determine a sonographic activity score [32] - [35] .
Ruess et al. stressed that a bowel wall thickness > 3 mm and increased bowel wall vascularity are correlated with common laboratory and clinical parameters of disease activity in patients with Crohn’s disease and ulcerative colitis [36] .
Haber et al., comparing US and histology in a population of 78 children, demonstrated a statistically significant relationship between maximal bowel wall thickness and disease activity, for both Crohn’s and RCU [29] . In our series we obtained similar results, with a statistically significant agreement (86.8%).
We compared the US findings [increased bowel wall thickness (using a threshold of 3 mm for the terminal ileum and 2 mm for the colon) and intramural vascularity at the site of thickening] with intestinal biopsies in the evaluation of the grade of disease activity.
In a study done by Reimund et al. of the US diagnostic value in Crohn’s disease and ulcerative colitis, the estimated sensitivity and specificity of US in the evaluation of disease activity were 94% and 67%, respectively [37] ; we obtained a similar sensitivity (80/93.3%) and higher specificity (86.8/100%).
Drews et al used the Limberg classification in a study including 32 adults, and demonstrated a significant association (p < 0.005) between the results of histology and bowel wall vascularity in the terminal ileum (n = 0.66; sensitivity 95%; specificity 69%) [20] . These findings were confirmed by Sasaki et al., who evaluated 108 Crohn’s patients, showing that the Limberg score reflects the endoscopic grade of activity, particularly in moderate and severe inflammation [38] . Using the same score we obtained similar results, with a significant association between US and histology (k = 0.81), comparable sensitivity (80/93.3%) and higher specificity (86.8/ 100%).
In a study including 44 children, Bremner et al. proposed that an increased bowel wall thickness in the ileum and in the colon has a high positive predictive value in moderate and severe inflammation [39] . In our study we found the highest PPV (100%) in inactive and severe inflammation, versus 73% and 88.9% in mild and moderate activity respectively.
MRE is another well established imaging modality that does not expose patients to ionizing radiation, and enables the study of IBD with conventional and functional sequences. DWI is a technique that uses the diffusion of water in biologic tissues to produce images: it provides functional, quantitative information about tissue cellularity [16] [40] .
Recently, in several studies, DWI-MRE, associated with ADC measurements, has been shown to reflect an abnormal activity in CD patients [41] [42] . Specifically, intestinal inflammatory lesions are characterized by a brighter signal in the b-value images and lower ADC values in normal segments. The reduction of ADC values in abnormal segments has been suggested to reflect an increased cellularity which, if present, would restrict the diffusion of the water molecules in the tissue [43] [44] .
Oto et al. evaluated 53 intestinal segments (19 pathologic and 34 controls) with DWI-MRE in 11 adult patients. ADC mean values were 1.59 ± 0.45 × 10−3 mm2/sec (range 0.46 - 2.50 × 10−3 mm2/sec) in cases of inflammation and 2.74 ± 0.68 × 10−3 mm2/sec (range 1.44 - 4.03 × 10−3 mm2/s) in normal segments [45] .
Kiryu et al. measured ADC values of the small and large bowel in 31 adults and compared the results of pathologic bowel segments to the normal ones: the ADC was lower in inflamed segments than healthy ones (Small bowel: 1.61 ± 0.44 × 10−3 mm2/sec vs 2.56 ± 0.51 × 10−3 mm2/sec. Large bowel: 1.52 ± 0.43 × 10−3 mm2/sec versus 2.31 ± 0.59 × 10−3 mm2/sec) [46] . Ream et al. studied a group of pediatric patients (mean age: 14.6 years) affected by Crohn’s disease. Mean ADC values of the inflamed bowel wall were 1.4 ± 0.3 × 10−3 mm2/sec [47] . In a population of 33 children, Neubauer et al retrospectively calculated ADC values of pathologic small bowel [0.84/1.40 × 10−3 mm2/sec (range 1.16 ± 0.18)] and colon [0.84/1.60 × 10−3 mm2/sec (1.21 ± 0.21)] [48] .
In a recent prospective research (2014) Tielbeek et al. made a comparison between dynamic contrast enhanced MRE (DCE-MRE) and DWI-ADC in affected adults; the results were referred to histology (AIS, acute inflammation score and FS, fibrosis score). The mean ADC value was 1988 (range 1216/4198): there was a trend towards decreased ADC values being associated with AIS, but this was not significant, while a decrease in ADC values was significantly correlated with FS [49] .
Our results were comparable with those of other studies involving children: mean ADC values were 0.837 ± 0.4 × 10−3 mm2/sec in our study, which are similar to the values previously reported by Ream (1.4 ± 0.3 × 10−3 mm2/sec) [47] and Neubauer (0.84/1.40 × 10−3 mm2/sec in the ileum and 0.84/1.60 × 10−3 mm2/sec in the colon) [48] .
As already observed by Ream et al, as compared to studies involving adults our results were slightly lower [47] . The mean ADC value was 0.837 ± 0.4 × 10−3 mm2/sec in our study vs: 1.59 ± 0.45 × 10−3 mm2/sec in Oto’s study [45] , 1.61 ± 0.44 × 10−3 mm2/sec and 1.52 ± 0.43 × 10−3 mm2/sec in the ileum and in the colon, respectively, in Kyriu’s study [46] and 1988 (1988 × 10−3) in Tielbeek’s study [49] .
In our experience the ADC values were negatively correlated to the disease severity and, assuming 1 × 10−3 mm2/sec as a cut off value, were useful to distinguish between inactive and moderate-severe active disease in 83.3% cases.
This study has some limitations. Firstly, the sample size is relatively small: this is partially due to the inclusion criterion that all patients included must have undergone US, MRI and intestinal biopsy during the same week.
Secondly, as the study is retrospective, we were limited to only two b-values (0 and 600 mm2/sec) (b-value measures the degree of the diffusion weighting applied. It indicates the amplitude (G), the time of applied gradients (δ) and the duration between the paired gradients (Δ). It is calculated as: b = γ2 G2 δ2 (Δ−δ/3) that were used for our routine DWI examinations; however, these b-values are similar to those described in previous studies [45] [47] [50] assessing DWI in children or adults.
Thirdly, the precise placement of ROIs on the ADC map is very challenging.
5. Conclusion
CD-US and DWI are useful in the evaluation of IBD severity and can have a particular value in the follow-up in childhood. Both techniques could be employed to identify disease flares, even in asymptomatic patients, to monitor the treatment and to evaluate surgical recurrence.
Acknowledgements
We would like to express our great appreciation to our TSRM Mr. Salvatore De Ceglie and Mr. Vito Savino, for their contribution to the collection of MR images and to Dr. Babette Pragnell for her precious help in the correction of written English.
Cite this paper
Salinaro Emanuela,Mancini Maria Elisabetta,De Venuto Domenica,Gallone Maria Filomena,Russo Silvana,Monteduro Mariantonietta,Angelelli Giuseppe, (2016) Color Doppler Ultrasonography and Diffusion Weighted Magnetic Resonance Enterography in Pediatric Ibd: Comparison with Histology in the Evaluation of Disease Severity. Open Access Library Journal,03,1-12. doi: 10.4236/oalib.1102406
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