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RESEARCH ARTICLE
Adv Biomed Res 2021,  10:38

Diagnostic accuracy of magnetic resonance cholangiopancreatography to detect benign and malignant biliary strictures


Department of Radiology, Isfahan University of Medical Sciences, Isfahan, Iran

Date of Submission07-Jun-2020
Date of Decision13-Jan-2021
Date of Acceptance14-Mar-2021
Date of Web Publication26-Nov-2021

Correspondence Address:
Dr. Shadi Ebrahimian
Department of Radiology, Isfahan University of Medical Sciences, Hezar Jerib Avenue, Isfahan
Iran
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Source of Support: The study was supported by Isfahan University of Medical Sciences, Conflict of Interest: None


DOI: 10.4103/abr.abr_137_20

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  Abstract 

Background: Magnetic resonance cholangiopancreatography (MRCP) is a noninvasive method to detect pancreaticobiliary strictures. In this study, we aimed to evaluate the diagnostic performance of MRCP and detect sensitive and specific radiologic features in distinguishing malignant and benign pathologies. Materials and Methods: In this study, 50 patients with biliary obstruction and a confirmed diagnosis using histopathology were included. The pathologies were evaluated using MRCP which were categorized into malignant and benign strictures. The etiology of strictures was detected using histopathology and endoscopic retrograde cholangiopancreatography. The diagnostic performance of MRCP was calculated using SPSS software. P < 0.05 was considered statistically significant. Results: Of 50 patients, 23 patients (46%) had malignant strictures based on MRCP and histopathology. The sensitivity and specificity of MRCP to detect malignancy were 95.7% and 96.3%, respectively. The most sensitive MRCP features to detect malignancy were upstream biliary duct dilation, abrupt tapering, and the presence of a solid mass with sensitivity 100%, 95.7%, and 78.2%, respectively. The malignancy rate was significantly higher in the strictures with length >11.5 mm or wall thickness >2.75 mm (P < 0.05). Conclusion: MRCP is a sensitive method to differentiate malignant lesions from benign pathologies. A long and thick stricture with the presence of a solid mass, upstream biliary duct dilation, and abrupt tapering is highly suggestive of malignancy.

Keywords: Biliary tract, Cholangiopancreatography, Magnetic Resonance, malignancy, pancreas


How to cite this article:
Shabanikia N, Adibi A, Ebrahimian S. Diagnostic accuracy of magnetic resonance cholangiopancreatography to detect benign and malignant biliary strictures. Adv Biomed Res 2021;10:38

How to cite this URL:
Shabanikia N, Adibi A, Ebrahimian S. Diagnostic accuracy of magnetic resonance cholangiopancreatography to detect benign and malignant biliary strictures. Adv Biomed Res [serial online] 2021 [cited 2023 Mar 30];10:38. Available from: https://www.advbiores.net/text.asp?2021/10/1/38/331279




  Introduction Top


Biliary obstruction has malignant and benign differential diagnosis. The most common cause of benign biliary obstruction is choledocholithiasis. However, cholangiocarcinoma, gallbladder carcinoma, or hepatocellular carcinoma are some causes of the malignant obstruction of biliary duct.[1] Since both benign and malignant obstruction causes can lead to late complications, accurate and early detection of disease is so important. In patients with a suspicious biliary stricture, the gold standard method to differentiate malignant lesions from benign lesions is histopathology which is an expensive and invasive procedure. However, imaging can differentiate benign and malignant lesions using the morphologic features of strictures.[2] Magnetic resonance cholangiopancreatography (MRCP) is a noninvasive technique which uses T2-weighted pulse sequences to detect pancreaticobiliary disorders. However, in some cases, differentiating the etiology of stricture is difficult. Some benign strictures mimic malignant strictures by increasing wall thickness and obstructing the lumen.[3],[4]

There are some studies on the morphologic features of strictures in benign and malignant pathologies. Shorter, smoother, and symmetric strictures with tapered margin were more likely to have a benign cause.[5] However, longer, thicker, asymmetric strictures with abrupt narrowing were suggestive of malignancy.[6] However, the prognostic value of these features was not measured in these studies.

This study aimed to evaluate role of MRCP in differentiating the causes of strictures due to the radiologic features. Moreover, we aimed to detect the most sensitive and specific MRCP findings suggestive pancreaticobiliary malignancies.


  Materials and Methods Top


It was a descriptive cross-sectional study which was performed from August 2018 to September 2019 on patients referred to the MRI center of Al-ZahraHospital Isfahan University of Medical Sciences, Isfahan, Iran. Patients older than 18 years with biliary obstruction due to MRCP and a definite diagnosis using biopsy were included in the study. Individuals with poor quality of the images or the presence of more than one simultaneous mass in ducts were not included.

This study's aim was explained to all patients, and informed consent was signed by them. The ethical board of the Radiology Department of Radiology, Isfahan University of Medical Sciences, approved the study. MRCP was performed using a 1.5-T MRI scanner (Ingenia, Philips). MRCP protocol is shown in [Table 1]. Patients were fasted for 4 h before the study. No antiperistaltic agent was used.
Table 1: Magnetic resonance imaging scan parameters

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Data collection including demographic information and imaging findings was done using designed forms. Imaging findings including length of stricture (in millimeter), asymmetrical or symmetrical narrowing, dilation of intrahepatic biliary radicle (IHBR), regular or irregular margin, abrupt or gradual tapering, partial or complete stricture, and presence or absence of other concomitant findings including mass, invasion to vessels, lymph node metastasis or organ spread, pancreatic parenchymal atrophy, and solid mass were recorded.

Irregular, long, asymmetric, or abrupt narrowing of the biliary and/or pancreatic duct were considered as malignant features. Besides, a narrow segment accompanied by solid mass, vascular and/or organ invasion, distal pancreatic parenchymal atrophy, distant metastases, or areas of low signal intensity in the pancreatic head on T1-weighted unenhanced images were considered as malignant stricture. Regular, short, and symmetric gradual tapering of the distal part of the duct with smooth contours and without total obstruction were used as the criteria for benignity.[7]

A final report on the benignity or malignancy of narrowing lesions was reached by consensual agreement between two radiologists who were blinded to the final diagnosis of the patients.

The histopathology and endoscopic retrograde cholangiopancreatography (ERCP) were used as the gold standard to detect the diagnostic values of MRCP, including sensitivity, specificity, negative predictive value (NPV), and positive predictive value (PPV). A Chi-square test was used to analyze different MRCP features in malignant and benign pathologies. A threshold for stricture length and wall thickness was detected using receiver operating characteristic (ROC) curve analyses. All analyses were done by SPSS software (SPSS Inc., Chicago, IL, USA). P < 0.05 was considered statistically significant.


  Results Top


Of 50 patients, 24 (48%) were female and 26 (52%) were male. History of the previous cholecystectomy was detected in 10 cases. Five patients had a history of non-pancreaticobiliary abdominal surgery. The most common site of strictures was the distal third of common bile duct (CBD) (19 cases). Other common locations were the porta hepatis (7 cases), the middle part of CBD (6 cases), the proximal part of CBD (4 cases), and the periampullary area (4 cases).

On MRCP, malignant appearing strictures were detected in 23 (46%) patients. Other 27 (54%) patients had benign appearing strictures using MRCP features. Histopathology revealed malignancy in 23 (46%) patients. 27 (54%) patients had benign mass using histopathology and ERCP findings as the gold standard. The most common etiologies of malignant strictures were pancreatic adenocarcinoma (39%) and cholangiocarcinoma (26%) [Figure 1]. Of 23 tumors with a definite malignancy diagnosis, 22 (95.7%) were correctly diagnosed on MRCP. Besides, MRCP could detect 26 of 27 (96.3%) benign lesions [Table 2]. The etiology of stricture in the patient with false-positive MRCP was postsurgical stricture.
Figure 1: Frequency of benign (a) and malignant strictures' etiology (b) IHBD: Intrahepatic biliary duct, CBD: Common bile duct

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Table 2: Diagnostic performance of magnetic resonance cholangiopancreatography in differentiating malignant and benign lesions

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The most common findings in MRCP were upstream biliary duct dilation (92%) and symmetrical dilation of the IHBR (86%). The frequency of other findings is shown in [Table 3].
Table 3: Frequency of different magnetic resonance cholangiopancreatography features of malignant and benign pancreaticobiliary strictures

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Irregular margin, abrupt tapering, the solid nature of the mass, invasion to surrounding tissue, presence of lymphadenopathy, upstream biliary duct dilation, and presence of duct penetrating sign were significantly more common in malignant tumors [Table 3]. Upstream biliary duct dilation, abrupt tapering, and solid mass presence were the most sensitive MRCP features in detecting malignancy with sensitivity 100%, 95.7%, and 78.2%, respectively [Table 4].
Table 4: Diagnostic performance of magnetic resonance cholangiopancreatography features in detecting malignancy

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The mean of stricture length and wall thickness was 16.62 ± 12.51 and 4.36 ± 3.84 mm, respectively. Stricture length and wall thickness were significantly higher among patients with malignant tumors (P < 0.05). Using ROC curve analysis, malignancy was more frequent in strictures with length more than 11.5 mm (P < 0.001, area under the curve [AUC] = 0.88, 95% confidence interval [CI] = 0.79–0.97) and wall thickness more than 2.75 mm (P < 0.001, AUC = 0.98, CI = 0.95–1.00) [Figure 2]. Stricture length >11.5 mm was able to detect malignant lesions with a sensitivity of 87% and specificity of 75%. The sensitivity and specificity of wall thickness to detect the malignant lesions were 95% and 93%, respectively.
Figure 2: Receiver operating characteristic cure analysis for wall thickness and stenosis length in distinguishing malignant strictures from benign pathologies

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  Discussion Top


This study was performed on 50 patients with abnormal MRCP and a confirmed diagnosis using histopathology and ERCP findings as the gold standard. The results of this study suggested MRCP as a sensitive and specific method to detect malignant strictures. Moreover, we found that among several radiologic features of strictures, margin irregularity, abrupt tapering, presence of solid mass, invasion to surrounding tissue, presence of lymphadenopathy, and upstream biliary duct dilation were more related to malignant lesions. Furthermore, stenosis length >11.5 mm and wall thickness >2.75 mm were more common among patients with malignant pathologies.

The reported sensitivity and specificity of MRCP to differentiate the benign and malignant lesions were 95.7% and 96.3%, respectively. The high sensitivity of MRCP to detect malignant strictures was reported in other studies.[7],[8] Suthar et al. reported a sensitivity of 85.7% and specificity of 96.3% for MRCP in detecting malignant strictures.[7] Saxena et al., in another study, found the sensitivity of 94%, the specificity of 94%, PPV of 97%, and NPV of 91%.[9] Margin irregularity in MRCP for suggesting malignancy was reported in the study of Abdelrahman et al.[10] However, they did not describe abrupt tapering as a cholangiographic criterion for malignancy diagnosis. Furthermore, in another study, abrupt ductal narrowing was seen in benign pathologies more commonly.[11] This is while, in the present study, abrupt tapering was significantly more common among malignant lesions. Abrupt tapering was able to predict the malignancy with a sensitivity of 96% and specificity of 74%. Although it was not a specific criterion for malignancy and it was also present in benign lesions, abrupt tapering should be considered as a malignant MRCP feature.

In our study, the presence of a mass was highly suggestive of a malignant stricture. Since the most common growth pattern of intrahepatic cholangiocarcinoma is a mass formation, more investigations are needed if a mass is detected in MRCP. However, extrahepatic cholangiocarcinomas are more likely to grow in an infiltrative pattern. Therefore, the absence of a mass does not rule out malignancy.[12]

The results of this study showed a higher frequency of symmetrical dilation of IHBR among benign lesions than malignant strictures. However, the difference was not statistically significant (P > 0.05). Moreover, asymmetrical dilation of biliary radicals was reported as a related feature to malignancy in some studies which is not consistent with our results.[7],[13]

The correlation between the length and thickness of stricture and malignancy was reported in many studies. In a study performed by Yu et al., the strictures were significantly thicker (4.4 mm) and longer (16.7 mm) in malignant lesions than benign pathologies.[14] Strictures with long segment narrowing were more likely to have an infiltrative growth pattern.[9] We detected a cutoff point 11.5 mm for the length of strictures which can predict the malignancy with a sensitivity of 87% and specificity of 75%. Furthermore, a wall thickness of more than 2.75 mm was highly suggestive of malignancy (sensitivity of 95% and specificity of 93%) in our study. Kim et al. also reported length <12 mm and thickness >3 mm as an indicator of malignancy which was similar to our results.[15]

Furthermore, Yu et al. reported a larger dilation of the upstream CBD in malignant strictures (21 mm) than benign strictures (16 mm), suggesting this feature as an MRCP finding of malignancy.[14] We measured the prognostic value of upstream dilation of the CBD and a sensitivity of 100% was detected. Although the sensitivity is high, the specificity was 15%, suggesting that the absence of upstream biliary duct dilation cannot rule out the malignancy.

In pancreatic duct stenosis, the absence of duct penetrating sign, the presence of complete stenosis, and the dilation of main or side branches of the pancreatic duct, were reported as a sign of adenocarcinoma.[16] In our study, although all three cases with the presence of duct penetrating sign had malignancy and idiopathic pancreatitis was not diagnosed in any of them, the sensitivity of this feature was low. However, a specificity of 100% was reported which suggests the absence of duct penetrating sign as an imaging feature in ruling out benign etiologies of stricture. Moreover, we reported complete stenosis and dilation of the main pancreatic duct with a higher frequency in malignant strictures. However, the difference was not significant.

Nonenhancing mural nodule ≥10 mm was as a malignancy predictor of intraductal papillary mucinous neoplasm. Ultrasonography was reported as the best method for detecting mural nodules.[17] However, MRCP was not sensitive enough in mural nodule detection.[18] In the present study, no mural nodule was detected in the MRCP of participants. This may be due to the absence of intraductal papillary mucinous neoplasm as the etiology of pancreatic cancers or low sensitivity of MRCP in finding mural nodules.

Pancreatic parenchymal atrophy was detected with a higher frequency among patients with malignant lesions than benign pathologies. However, it was not statistically different. The results show that the atrophy of pancreatic parenchyma cannot be related to malignancy. In another study done on 178 patients, a high degree of pancreatic atrophy was not associated to the pancreatic ductal adenocarcinoma with intraductal papillary mucinous neoplasm.[19] Since the degree of pancreatic parenchymal atrophy may vary among different types of cancers, more studies are needed to distinguish parenchymal changes in malignancies.


  Conclusion Top


The results showed that the strictures with a length >11.5 mm and wall thickness >2.75 mm are highly suggestive for cholangiocarcinoma. We found upstream biliary duct dilation, abrupt tapering, and the presence of a solid mass as the most sensitive features. Lymphadenopathy, invasion to surrounding tissue, margin irregularity, and presence of a solid mass were the most specific findings to detect cholangiocarcinoma using MRCP. In addition, the absence of a duct penetrating sign was a specific radiologic feature in detecting pancreatic adenocarcinoma.

Acknowledgment

We would like to express our great thanks to Dr. Mohsen Hosseini because of his valuable consultation in doing the statistical analysis.

Financial support and sponsorship

The study was supported by Isfahan University of Medical Sciences.

Conflicts of interest

There are no conflicts of interest.



 
  References Top

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Griffin N, Charles-Edwards G, Grant LA. Magnetic resonance cholangiopancreatography: The ABC of MRCP. Insights Imaging 2012;3:11-21.  Back to cited text no. 4
    
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Wang Y, Wang Y, Yang T, Chen Y. Value of Magnetic Resonance Cholangiopancreatography Combined with Dynamic Contrast Enhanced CT in Differential Diagnosis of Benign and Malignant Biliary Stricture; 2017;28;16.  Back to cited text no. 5
    
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Rajab L. Correlation of MRCP and Surgical Findings in Patients with Obsructive Jaundice at MNH: Muhimbili University of Health and Allied Sciences; 2017.  Back to cited text no. 6
    
7.
Suthar M, Purohit S, Bhargav V, Goyal P. Role of MRCP in differentiation of benign and malignant causes of biliary obstruction. J Clin Diagn Res 2015;9:TC08-12.  Back to cited text no. 7
    
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Dillman JR, Patel RM, Lin TK, Towbin AJ, Trout AT. Diagnostic performance of magnetic resonance cholangiopancreatography (MRCP) versus endoscopic retrograde cholangiopancreatography (ERCP) in the pediatric population: A clinical effectiveness study. Abdom Radiol (NY) 2019;44:2377-83.  Back to cited text no. 8
    
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Saxena S, Prajapati D, Doctor M, Patel H. Role of 3T magnetic resonance cholangiopancreatography (MRCP) in biliary strictures in adult population of western India. Int J Sci Res 2019;8:63-66.  Back to cited text no. 9
    
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Abdelrahman AS, Muhammed ZM. Role of magnetic resonance cholangio-pancreaticography in differentiating between benign and malignant causes of biliary obstruction. Egypt J Hosp Med 2017;68:954-66.  Back to cited text no. 10
    
11.
Katabathina VS, Dasyam AK, Dasyam N, Hosseinzadeh K. Adult bile duct strictures: Role of MR imaging and MR cholangiopancreatography in characterization. Radiographics 2014;34:565-86.  Back to cited text no. 11
    
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Lee WJ, Lim HK, Jang KM, Kim SH, Lee SJ, Lim JH, et al. Radiologic spectrum of cholangiocarcinoma: Emphasis on unusual manifestations and differential diagnoses. Radiographics 2001;21:S97-116.  Back to cited text no. 12
    
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Joo I, Lee JM, Yoon JH. Imaging diagnosis of intrahepatic and perihilar cholangiocarcinoma: Recent advances and challenges. Radiology 2018;288:7-13.  Back to cited text no. 13
    
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Yu XR, Huang WY, Zhang BY, Li HQ, Geng DY. Differentiation of infiltrative cholangiocarcinoma from benign common bile duct stricture using three-dimensional dynamic contrast-enhanced MRI with MRCP. Clin Radiol 2014;69:567-73.  Back to cited text no. 14
    
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Kim JY, Lee JM, Han JK, Kim SH, Lee JY, Choi JY, et al. Contrast-enhanced MRI combined with MR cholangiopancreatography for the evaluation of patients with biliary strictures: Differentiation of malignant from benign bile duct strictures. J Magn Reson Imaging 2007;26:304-12.  Back to cited text no. 15
    
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Boninsegna E, Manfredi R, Negrelli R, Avesani G, Mehrabi S, Pozzi Mucelli R. Pancreatic duct stenosis: Differential diagnosis between malignant and benign conditions at secretin-enhanced MRCP. Clin Imaging 2017;41:137-43.  Back to cited text no. 16
    
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Kawada N, Uehara H, Nagata S, Tsuchishima M, Tsutsumi M, Tomita Y. Mural nodule of 10 mm or larger as predictor of malignancy for intraductal papillary mucinous neoplasm of the pancreas: Pathological and radiological evaluations. Pancreatology 2016;16:441-8.  Back to cited text no. 17
    
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    Figures

  [Figure 1], [Figure 2]
 
 
    Tables

  [Table 1], [Table 2], [Table 3], [Table 4]



 

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