<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">IJMPCERO</journal-id><journal-title-group><journal-title>International Journal of Medical Physics, Clinical Engineering and Radiation Oncology</journal-title></journal-title-group><issn pub-type="epub">2168-5436</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/ijmpcero.2020.91003</article-id><article-id pub-id-type="publisher-id">IJMPCERO-97619</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Medicine&amp;Healthcare</subject><subject> Physics&amp;Mathematics</subject></subj-group></article-categories><title-group><article-title>
 
 
  The Usefulness of Diffusion Weighted and Contrast Enhanced Magnetic Resonance Imaging in Characterization of Inconclusive Ovarian Mass
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Ghada</surname><given-names>Mohammed Abd El Razeq</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Mohammad</surname><given-names>A. M. Ahmed</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Department of Radiodiagnosis, Qena Faculty of Medicine, South Valley University, Qena, Egypt</addr-line></aff><aff id="aff2"><addr-line>Department of Obstetrics &amp;amp; Gynecology, Qena Faculty of Medicine, South Valley University, Qena, Egypt</addr-line></aff><pub-date pub-type="epub"><day>10</day><month>12</month><year>2019</year></pub-date><volume>09</volume><issue>01</issue><fpage>24</fpage><lpage>33</lpage><history><date date-type="received"><day>29,</day>	<month>November</month>	<year>2019</year></date><date date-type="rev-recd"><day>31,</day>	<month>December</month>	<year>2019</year>	</date><date date-type="accepted"><day>3,</day>	<month>January</month>	<year>2020</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  Introduction: Ovarian cancer is the commonest reason for death in females due to gynecologic malignancy around the world. In contrast to other gynecologic tumours, the definitive diagnosis is accomplished days after of the index surgery by the histopathology. Preoperative assessment based on conventional MRI is not accurate. Information is expanding increasing about the ability of new MRI modalities to assess ovarian mass. 
  Aim of the study: To assess the ability of dynamic contrast-enhanced MRI (DCE–MRI), and Diffusion-weighted image (DWI) to describe uncertain ovarian masses. 
  Patients and Methods: This is a retrospective study. Patients were referred from radio-diagnosis department and gynecology department of Qena faculty of medicine hospitals, South Valley University. Patients had uncertain adnexal masses at ultrasound. Magnetic resonance examination was doneutilizing 1.5 Tesla machine. The protocol included T1WI, T2WI, T1WI following contrast, and DWI. 
  Results: We included 44 patients with different forms of complex cystic and solid ovarian masses. The final pathology of the ovarian masses was 18 benign, 4 borderline, and 22 malignant. The sensitivity, specificity, positive predictive value, negative predictive value, and accuracy for DWI were 100%, 94.4%, 96.3%, 100%, and 97.7% respectively. The performance of DWI was higher than the conventional MRI and DCE-MRI. 
  Conclusion: DCE-MRI and DWI have accepted ability to recognize malignant ovarian mass.
 
</p></abstract><kwd-group><kwd>Ovarian</kwd><kwd> Contrast</kwd><kwd> Diffusion</kwd><kwd> MRI</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Ovarian cancer is one of the commonest cancers in the world. It is the commonest cause of death in women due to gynecologic malignancy around the world. It has a 5 year survival of 40% [<xref ref-type="bibr" rid="scirp.97619-ref1">1</xref>]. In contrast to other gynecologic cancers, the definitive diagnosis is achieved days after of the index surgery. The diagnosis is by pathology. Preoperative diagnosis based on clinical, laboratory, radiological, and even frozen section is not free of errors [<xref ref-type="bibr" rid="scirp.97619-ref2">2</xref>]. Preoperative biopsy is not offered except when the planed treatment is neoadjuvant chemotherapy or in palliative settings [<xref ref-type="bibr" rid="scirp.97619-ref3">3</xref>].</p><p>Ultrasound is the first diagnostic imaging. Conventional Magnetic resonance imaging (MRI) uses T1 &amp; T2 signals. MRI has 76% sensitivity and 97% specificity for diagnosis of uncertain ovarian mass. DCE-MRI has a higher sensitivity and specificity of 81% &amp; 98% (DCE-MRI) [<xref ref-type="bibr" rid="scirp.97619-ref4">4</xref>].</p><p>DWI is another modality in MRI. It depends on the different microstructure, cellular density, and microvasculature of malignant tissue. In ordinary body structure, water molecules move freely. Water in malignant tissue has restricted ability to diffuse. The apparent diffusion coefficient (ADC) value is a quantitative measure of diffusion. The computer unit in the MRI machine changes these quantities into a user-friendly qualitative image. This is the DWI. Tissues with limited diffusion are white on DWI and hypointense on the ADC map [<xref ref-type="bibr" rid="scirp.97619-ref5">5</xref>].</p><p>Earlier reports on the ability of DWI to recognize malignant ovarian tumour have found that DWI is not useful [<xref ref-type="bibr" rid="scirp.97619-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.97619-ref7">7</xref>]. Later reports found that DWI is useful in discrimination between benign and malignant ovarian mass [<xref ref-type="bibr" rid="scirp.97619-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.97619-ref9">9</xref>] [<xref ref-type="bibr" rid="scirp.97619-ref10">10</xref>]. A more recent study found a sensitivity of 84%, and a specificity of 89% [<xref ref-type="bibr" rid="scirp.97619-ref11">11</xref>].</p><p>Information is expanding on the diagnostic ability of DCE-MRI and DWI. In this study, we expect to evaluate the ability of DCE–MRI, and DWI to describe uncertain ovarian masses.</p><p>Aim of the study: to assess the ability of dynamic contrast-enhanced MRI (DCE–MRI), and Diffusion-weighted image (DWI) to describe uncertain ovarian masses.</p></sec><sec id="s2"><title>2. Patients and Methods</title><p>Design: a comparative study.</p><p>Patients: Patients were recruited from radio-diagnosis department &amp; gynecology department of Qena faculty of medicine hospitals, South Valley University. The study started from 1<sup>st</sup> of July 2018 to 30<sup>th</sup> of July 2019.</p><p>Patients had inconclusive adnexal masses at ultrasound. Masses satisfy any of the following criteria: 1) solid; 2) complex (solid and cystic); or 3) cystic with papillary projections or septations. Masses that obviously determined by ultrasound were out of the research.</p><p>Ethical considerations: written consents were obtained from participants. Patient data were anonymized. The ethical committee of research in our college approved the study.</p></sec><sec id="s3"><title>3. Methods</title><p>We did transabdominal ultrasound and transvaginal ultrasound for all cases. We used GE Logic P6 ultrasound machine (GE Healthcare Medical system; USA). We pursue the International Ovarian Tumor Analysis (IOTA) rules to characterize ovarian mass [<xref ref-type="bibr" rid="scirp.97619-ref12">12</xref>]. MR assessment was done at the magnetic resonance unit, Qena faculty of medicine Hospital, South Valley University. We used 1.5 Tesla amachine with body coil as a transmitter and a receiver of radio frequency signals (Achieva, Philips Medical System; Netherland). The MR assessment included T1WI, T2WI, post-contrast fat-suppressed T1WI, and DWI. DWI was done at b0, b500, b1000. Descriptive analysis was done. Data from the MR assessment included the mean size of the cyst or mass, the ADC value, and the morphologic criteria suggesting malignancy. We had executed an individual analysis for conventional MRI, DCE-MRI and DWI concerning their diagnostic performance in the characterization of ovarian masses/cysts. Masses are sent for histopathology after operations.</p></sec><sec id="s4"><title>4. Results</title><p>We investigated 50 patients with 50 adnexal lesions. Six masses were omitted, three of them due to loss of follow up. Unfortunately, we excluded one mass because of lack of pathology (patient died before operation). Two masses are excluded, as they were broad-ligamentary fibroid. The remaining 44 patients with 44 complex ovarian masses were included in our study.</p><p>The patient’s age ranged from 20 to 78 years old (mean 43.56 years). The main complaint was abdominal pain and/or abdominal distension; other cases came with different symptoms as subfertility or irregular vaginal bleeding.</p><p>The histopathology of the assessed masses were 18 benign, 4 borderline, and 22 malignant. The age range for patients with benign tumors was 20 - 65 years (mean 39 &#177; 13 years), while those with malignant tumors, their age range was 21 - 78 years (mean 46 &#177; 16.953 years).</p><p>Benign masses included six serous cystadenoma, five mucinous cysadenoma, three mature cystic teratoma, two ovarian fibroma, and fibrothecoma, and one tubo-ovarian abscess. There were four Borderline tumors (two serous and two mucinous). There were 22 invasive malignant masses (seven Serous cyst-adeno- carcinoma, five Mucinous cyst-adenocarcinoma, three Metastatic krukenburg, three Immature teratoma, two fibrosarcoma, and two clear cell carcinoma).</p><p>The analysis of the size of the lesions is appeared in <xref ref-type="table" rid="table1">Table 1</xref>. The malignant and borderline ovarian lesions were bigger than the benign lesions.</p><p>The complex ovarian masses showed variable signal intensities in T1 and T2 as follows:</p><p>For T1 signal intensity, 34 of the included ovarian masses showed is o-intense signal intensity, 2 masses showed bright signals, while 8 masses showed mixed signal intensities. For T2 signal intensity, 32 of the masses showed high signals</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Analysis of the ovarian lesions size</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Dimension</th><th align="center" valign="middle" >Benign</th><th align="center" valign="middle" >Borderline</th><th align="center" valign="middle" >Malignant</th></tr></thead><tr><td align="center" valign="middle" >Minimum</td><td align="center" valign="middle" >4.5 cm</td><td align="center" valign="middle" >6 cm</td><td align="center" valign="middle" >7 cm</td></tr><tr><td align="center" valign="middle" >Maximum</td><td align="center" valign="middle" >15 cm</td><td align="center" valign="middle" >22 cm</td><td align="center" valign="middle" >25 cm</td></tr><tr><td align="center" valign="middle" >Mean &#177; SD</td><td align="center" valign="middle" >9.7 &#177; 3.3</td><td align="center" valign="middle" >14 &#177; 7.3</td><td align="center" valign="middle" >13.7 &#177; 5.08</td></tr></tbody></table></table-wrap><p>and 12 masses showed mixed signals (Figures 2-5). ADC values of malignant tumors showed a minimum of 0.7 &#215; 10<sup>−</sup><sup>3</sup> mm<sup>2</sup>/s and a maximum of 1.2 &#215; 10<sup>−</sup><sup>3</sup> mm<sup>2</sup>/s. The mean (&#177;SD) was 1.01 &#215; 10<sup>−</sup><sup>3</sup> mm<sup>2</sup>/s (&#177;0.34), while ADC values of the benign masses showed a minimum of 1.2 &#215; 10<sup>−</sup><sup>3</sup> mm<sup>2</sup>/s and maximum of 2 &#215; 10<sup>−</sup><sup>3</sup> mm<sup>2</sup>/s with mean &#177;SD 1.6 &#215; 10<sup>−</sup><sup>3</sup> mm<sup>2</sup>/s (&#177;0.27). The mean ADC value in benign tumors was obviously higher than that in malignant ones (Figures 1-5 &amp; <xref ref-type="table" rid="table2">Table 2</xref>).</p><p>For the sake of statistical evaluation, we incorporated the borderline tumors into the classification of malignant tumors. The histopathological reported 26 malignant and 18 benign lesions. The performance of the preoperative imaging is outlined in <xref ref-type="table" rid="table3">Table 3</xref>. The sensitivity, specificity, positive predictive value, negative predictive value, and accuracy for DWI were 100%, 94.4%, 96.3%, 100%, and 97.7% respectively. The performance of DWI was higher than the conventional MRI and DCE-MRI. Borderline and malignant ovarian tumors showed restricted diffusion. Benign tumors had facilitated diffusion (Figures 2-5).</p></sec><sec id="s5"><title>5. Discussion</title><p>Ovarian carcinoma has the most elevated death rate among tumours of the female genital tract. Differentiation between benign and malignant ovarian tumor is vital to offer the appropriate plan for each case [<xref ref-type="bibr" rid="scirp.97619-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.97619-ref13">13</xref>].</p><p>Conventional MRI assesses morphologic criteria of the lesion, such as wall thickening, intra luminal papilla, mural nodules, thick septae, and signal intensity on T1WI and T2WI. None of these criteria can consistently segregate benign from malignant lesions [<xref ref-type="bibr" rid="scirp.97619-ref4">4</xref>]. Development of novel MRI modalities like DCE MRI and DWI improves the diagnostic performance of MRI [<xref ref-type="bibr" rid="scirp.97619-ref4">4</xref>].</p><p>We had executed an individual analysis for conventional MRI, DCE-MRI and DWI concerning their diagnostic performance in the characterization of ovarian masses/cysts. We found that conventional MRI had 88.5% sensitivity and 72.2% specificity. This looks well with a meta-analysis of the value of MRI in characterization of ovarian mass/cyst in women with non-conclusive ultrasound evaluation. They found that the sensitivity and specificity was 76% and 97%, respectively [<xref ref-type="bibr" rid="scirp.97619-ref14">14</xref>].</p><p>We found that DCE-MRI had 92.3% sensitivity and 88.8% specificity. This compares favourably to conventional MRI in our study. So, adding DCE to the MRI increased the accuracy of examination. Systematic review showed that DCE-MRI has 81% sensitivity and 98% specificity [<xref ref-type="bibr" rid="scirp.97619-ref14">14</xref>]. However, a more recent study showed 83% sensitivity and 75% specificity [<xref ref-type="bibr" rid="scirp.97619-ref15">15</xref>]. Malignant masses showed</p><p>more intense enhancement than benign lesions. Difference was clearer in the early phase of the contrast study than the late phase [<xref ref-type="bibr" rid="scirp.97619-ref16">16</xref>] [<xref ref-type="bibr" rid="scirp.97619-ref17">17</xref>].</p><p>Our analysis revealed that DWI has 100% sensitivity, 94.4% specificity, 96.3% PPV, 100% NPV, and 97.7% accuracy. The performance of DWI was higher than conventional MRI and DCE-MRI. We found that all malignant lesions and one</p><p>case of dermoid cyst demonstrated a high signal on DWI. This may be ascribed to keratinized substance in dermoid cyst. These results are consistent with the conclusions in the previous researches. They showed that most of the malignant ovarian masses and some of the dermoid cysts had high intensity on DWI. Most of the benign lesions had low signal intensity on DWI [<xref ref-type="bibr" rid="scirp.97619-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.97619-ref18">18</xref>] [<xref ref-type="bibr" rid="scirp.97619-ref19">19</xref>].</p><p>In our study, the mean ADC values for malignant lesions were 1.01 &#215; 10<sup>−</sup><sup>3</sup> &#177; 0.34 mm<sup>2</sup>/s). The mean ADC values for benign lesions were (1.6 &#215; 10<sup>−</sup><sup>3</sup> &#177; 0.27 mm<sup>2</sup>/s). Our cut-off value was 1.2 &#215; 10<sup>−</sup><sup>3</sup> mm<sup>2</sup>/s. This agreed with findings by Takeuchi et al. They found the mean ADC value was 1.03 &#215; 10<sup>−</sup><sup>3</sup> mm<sup>2</sup>/sin malignant tumors and 1.38 &#215; 10<sup>−</sup><sup>3</sup> mm<sup>2</sup>/s in benign tumor [<xref ref-type="bibr" rid="scirp.97619-ref17">17</xref>]. A meta-analysis of 16 studies showed that DWI is able to distinguish between benign and malignant ovarian tumor with 91% sensitivity and 91% specificity [<xref ref-type="bibr" rid="scirp.97619-ref20">20</xref>].</p><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Showing the different ADC values of the included masses</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Pathological type</th><th align="center" valign="middle" >ADV value (Range)</th></tr></thead><tr><td align="center" valign="middle" >BENIGN</td><td align="center" valign="middle" >1.2 - 2 &#215; 10<sup>−</sup><sup>3</sup> mm<sup>2</sup>/sec</td></tr><tr><td align="center" valign="middle" >Serous cystadenoma</td><td align="center" valign="middle" >1.4 - 2 &#215; 10<sup>−</sup><sup>3</sup> mm<sup>2</sup>/sec</td></tr><tr><td align="center" valign="middle" >Mucinous cystadenoma</td><td align="center" valign="middle" >1.3 - 1.5 &#215; 10<sup>−</sup><sup>3</sup> mm<sup>2</sup>/sec</td></tr><tr><td align="center" valign="middle" >Mature cystic teratoma</td><td align="center" valign="middle" >1.2 - 1.5 &#215; 10<sup>−</sup><sup>3</sup> mm<sup>2</sup>/sec</td></tr><tr><td align="center" valign="middle" >Ovarian fibroma</td><td align="center" valign="middle" >1.6 - 1.8 &#215; 10<sup>−</sup><sup>3</sup> mm<sup>2</sup>/sec</td></tr><tr><td align="center" valign="middle" >Fibrothecoma</td><td align="center" valign="middle" >1.2 &#215; 10<sup>−</sup><sup>3</sup> mm<sup>2</sup>/sec</td></tr><tr><td align="center" valign="middle" >Tubo-ovarian abscess</td><td align="center" valign="middle" >1.3 &#215; 10<sup>-3</sup> mm<sup>2</sup>/sec</td></tr><tr><td align="center" valign="middle" >MALIGNANT</td><td align="center" valign="middle" >0.7 - 1.2 &#215; 10<sup>−</sup><sup>3</sup> mm<sup>2</sup>/sec</td></tr><tr><td align="center" valign="middle" >Serous cystadenocarcinoma</td><td align="center" valign="middle" >0.7 - 1 &#215; 10<sup>−</sup><sup>3</sup> mm<sup>2</sup>/sec</td></tr><tr><td align="center" valign="middle" >Mucinous cystadenocarcinoma</td><td align="center" valign="middle" >0.9 &#215; 10<sup>−</sup><sup>3</sup> mm<sup>2</sup>/sec</td></tr><tr><td align="center" valign="middle" >Metastatic Krukenberg</td><td align="center" valign="middle" >1.2 &#215; 10<sup>−</sup><sup>3</sup> mm<sup>2</sup>/sec</td></tr><tr><td align="center" valign="middle" >Clear cell carcinoma</td><td align="center" valign="middle" >0.9 &#215; 10<sup>−</sup><sup>3</sup> mm<sup>2</sup>/sec</td></tr><tr><td align="center" valign="middle" >Fibrosarcoma</td><td align="center" valign="middle" >1.1 &#215; 10<sup>−</sup><sup>3</sup> mm<sup>2</sup>/sec</td></tr><tr><td align="center" valign="middle" >Immature teratoma</td><td align="center" valign="middle" >0.8 - 0.9 &#215; 10<sup>−</sup><sup>3</sup> mm<sup>2</sup>/sec</td></tr><tr><td align="center" valign="middle" >Borderline serous neoplasm</td><td align="center" valign="middle" >1.1 - 1.5 &#215; 10<sup>−</sup><sup>3</sup> mm<sup>2</sup>/sec</td></tr><tr><td align="center" valign="middle" >Borderline mucinous neoplasm</td><td align="center" valign="middle" >1.2 &#215; 10<sup>−</sup><sup>3</sup> mm<sup>2</sup>/sec</td></tr></tbody></table></table-wrap><table-wrap id="table3" ><label><xref ref-type="table" rid="table3">Table 3</xref></label><caption><title> The performance of the preoperative diagnosis</title></caption><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" >Ultrasound</th><th align="center" valign="middle" >Conventional MRI</th><th align="center" valign="middle" >DCE-MRI</th><th align="center" valign="middle" >DWI</th></tr></thead><tr><td align="center" valign="middle" >TP</td><td align="center" valign="middle" >20</td><td align="center" valign="middle" >23</td><td align="center" valign="middle" >24</td><td align="center" valign="middle" >26</td></tr><tr><td align="center" valign="middle" >FN</td><td align="center" valign="middle" >6</td><td align="center" valign="middle" >3</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >0</td></tr><tr><td align="center" valign="middle" >FP</td><td align="center" valign="middle" >6</td><td align="center" valign="middle" >5</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >1</td></tr><tr><td align="center" valign="middle" >TN</td><td align="center" valign="middle" >12</td><td align="center" valign="middle" >13</td><td align="center" valign="middle" >16</td><td align="center" valign="middle" >17</td></tr><tr><td align="center" valign="middle" >Sensitivity</td><td align="center" valign="middle" >76.9 %</td><td align="center" valign="middle" >88.5 %</td><td align="center" valign="middle" >92.3 %</td><td align="center" valign="middle" >100 %</td></tr><tr><td align="center" valign="middle" >Specificity</td><td align="center" valign="middle" >66.6 %</td><td align="center" valign="middle" >72.2 %</td><td align="center" valign="middle" >88.8 %</td><td align="center" valign="middle" >94.4 %</td></tr><tr><td align="center" valign="middle" >PPV</td><td align="center" valign="middle" >76.9 %</td><td align="center" valign="middle" >82.1 %</td><td align="center" valign="middle" >85.7 %</td><td align="center" valign="middle" >96.3 %</td></tr><tr><td align="center" valign="middle" >NPV</td><td align="center" valign="middle" >66.6 %</td><td align="center" valign="middle" >81.2 %</td><td align="center" valign="middle" >88.8 %</td><td align="center" valign="middle" >100 %</td></tr><tr><td align="center" valign="middle" >Accuracy</td><td align="center" valign="middle" >72.2 %</td><td align="center" valign="middle" >81.8 %</td><td align="center" valign="middle" >90.9 %</td><td align="center" valign="middle" >97.7 %</td></tr></tbody></table></table-wrap><p>Limitations of the study: we did analysis of heterogonous group of tumors. Therefore, the absolute number of each tumour is small. Tumors have variable criteria according to their specific histologic composition. A larger study with focus on specific tumour type is needed.</p></sec><sec id="s6"><title>6. Conclusion</title><p>DCE-MRI and DWI have accepted ability to distinguish between benign and malignant ovarian mass.</p></sec><sec id="s7"><title>7. Recommendations</title><p>We recommend adding DCE-MRI and DWI to the conventional MRI in the assessment of ovarian mass. This will aid in accurate diagnosis. Further researches are needed to build up cumulative evidence of the value of novel signals of MRI.</p></sec><sec id="s8"><title>Authors’ Approval</title><p>Authors read and approve the manuscript. All authors have fulfilled the requirements for authorship. Each author believes that the manuscript represents honest work. This manuscript is not considered for publishing anywhere else.</p></sec><sec id="s9"><title>Conflicts of Interest</title><p>We have no conflict of interest to disclose. We received no funding.</p></sec><sec id="s10"><title>Cite this paper</title><p>El Razeq, G.M.A. and Ahmed, M.A.M. (2020) The Usefulness of Diffusion Weighted and Contrast Enhanced Magnetic Resonance Imaging in Characterization of Inconclusive Ovarian Mass. International Journal of Medical Physics, Clinical Engineering and Radiation Oncology, 9, 24-33. https://doi.org/10.4236/ijmpcero.2020.91003</p></sec></body><back><ref-list><title>References</title><ref id="scirp.97619-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Momenimovahed, Z., Tiznobaik, A., Taheri, S. and Salehiniya, H. (2019) Ovarian Cancer in the World: Epidemiology and Risk Factors. 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