Abstract
Purpose
To reveal the prevalence of small (≤ 20 mm) pancreatic ductal carcinomas with enhanced rims on triple-phase contrast-enhanced CT and correlate the CT images with the pathologic findings.
Materials and methods
Between April 2005 and April 2016, 45 patients underwent preoperative triple-phase contrast-enhanced CT and were pathologically diagnosed with small pancreatic ductal carcinoma. CT images were independently reviewed by two radiologists. The attenuation values of the enhanced rims, internal areas of the tumors, and surrounding pancreatic parenchyma were compared using Mann–Whitney U test. These areas were also correlated with the pathologic findings. Tumor invasiveness was compared between the tumors with and without enhanced rims using Fisher’s exact test.
Results
Enhanced rims were identified in 18 tumors (40%) by consensus between the two reviewers. The enhanced rims showed significantly higher mean attenuation values compared with the internal areas of the tumors (p < 0.001) and surrounding pancreatic parenchyma (p < 0.0086), and were most clearly visualized on equilibrium phase. The enhanced rims pathologically reflected the abundant fibrotic stroma with cancer cells in all tumors. There was no statistically significant difference in tumor invasiveness between the tumors with and without enhanced rims (anterior peripancreatic invasion, p = 0.137; posterior peripancreatic invasion, p = 0.758; portal vein invasion, p = 0.639; and lymph node metastases, p = 0.359).
Conclusions
Enhanced rims were detected at a rate of 40% in small pancreatic ductal carcinomas and could be an important finding for diagnosis on CT images, but did not suggest a less aggressive nature.
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References
Rao SX, Zeng MS, Cheng WZ, et al. (2011) Small solid tumors (≤ 2 cm) of the pancreas: relative accuracy and differentiation of CT and MR imaging. Hepatogastroenterology 58:996–1001
Choi TW, Lee JM, Kim JH, et al. (2016) Comparison of multidetector CT and gadobutrol-enhanced MR imaging for evaluation of small, solid pancreatic lesions. Korean J Radiol 17:509–521
Yoon SH, Lee JM, Cho JY, et al. (2011) Small (≤ 20 mm) pancreatic adenocarcinomas: analysis of enhancement patterns and secondary signs with multiphasic multidetector CT. Radiology 259:442–452
Dietrich CF, Sahai AV, D’Onofrio M, et al. (2016) Differential diagnosis of small solid pancreatic lesions. Gastrointest Endosc 84:933–940
Yu MH, Lee JY, Kim MA, et al. (2010) MR imaging features of small solid pseudopapillary tumors: retrospective differentiation from other small solid pancreatic tumors. AJR 195:1324–1332
Kamisawa T, Wood LD, Itoi T, Takaori K (2016) Pancreatic cancer. Lancet 388:73–85
Xu Z, Pothula SP, Wilson JS, Apte MV (2014) Pancreatic cancer and its stroma: a conspiracy theory. World J Gastroenterol 20:11216–11229
Gleason MX, Mdzinarishvili T, Are C, et al. (2013) Prognostic estimator of survival for patients with localized and extended pancreatic ductal adenocarcinoma. Cancer Inform 12:103–114
Prokesch RW, Chow LC, Beaulieu CF, Bammer R, Jeffrey RB Jr (2002) Isoattenuating pancreatic adenocarcinoma at multi-detector row CT: secondary signs. Radiology 224:764–768
Ishigami K, Yoshimitsu K, Irie H, et al. (2009) Diagnostic value of the delayed phase image for iso-attenuating pancreatic carcinomas in the pancreatic parenchymal phase on multidetector computed tomography. Eur J Radiol 69:139–146
Yamada Y, Mori H, Matsumoto S, et al. (2010) Pancreatic adenocarcinoma versus chronic pancreatitis: differentiation with triple-phase helical CT. Abdom Imaging 35:163–171
Furuhashi N, Suzuki K, Sakurai Y, et al. (2015) Differentiation of focal-type autoimmune pancreatitis from pancreatic carcinoma: assessment by multiphase contrast-enhanced CT. Eur Radiol 25:1366–1374
Tamada T, Ito K, Kanomata N, et al. (2016) Pancreatic adenocarcinomas without secondary signs on multiphasic multidetector CT: association with clinical and histopathologic features. Eur Radiol 26:646–655
Landis JR, Koch GG (1977) The measurement of observer agreement for categorical data. Biometrics 33:159–174
Greenlee RT, Murray T, Bolden S, Wingo PA (2000) Cancer statistics, 2000. CA Cancer J Clin 50:7–33
Lau MK, Davila JA, Shaib YH (2010) Incidence and survival of pancreatic head and body and tail cancers: a population-based study in the United States. Pancreas 39:458–462
Matsuno S, Egawa S, Fukuyama S, et al. (2004) Pancreatic cancer registry in Japan: 20 years of experience. Pancreas 28:219–230
Asayama Y, Yoshimitsu K, Irie H, et al. (2006) Delayed-phase dynamic CT enhancement as a prognostic factor for mass-forming intrahepatic cholangiocarcinoma. Radiology 238:150–155
Hwang RF, Moore T, Arumugam T, et al. (2008) Cancer-associated stromal fibroblasts promote pancreatic tumor progression. Cancer Res 68:918–926
Kalluri R, Zeisberg M (2006) Fibroblasts in cancer. Nat Rev Cancer 6:392–401
von Ahrens D, Bhagat TD, Nagrath D, Maitra A, Verma A (2017) The role of stromal cancer-associated fibroblasts in pancreatic cancer. J Hematol Oncol 10:76
Chiou YY, Chiang JH, Hwang JI, et al. (2004) Acinar cell carcinoma of the pancreas: clinical and computed tomography manifestations. J Comput Assist Tomogr 28:180–186
Hsu MY, Pan KT, Chu SY, et al. (2010) CT and MRI features of acinar cell carcinoma of the pancreas with pathologic correlations. Clin Radiol 65:223–229
Raman SP, Hruban RH, Cameron JL, et al. (2013) Acinar cell carcinoma of the pancreas: computed tomography features–a study of 15 patients. Abdom Imaging 38:137–143
Yin Q, Wang M, Wang C, et al. (2012) Differentiation between benign and malignant solid pseudopapillary tumor of the pancreas by MDCT. Eur J Radiol 81:3010–3018
Huang YS, Chen JL, Chang CC, Liu KL (2014) Solid pseudopapillary neoplasms of the pancreas: imaging differentiation between benignity and malignancy. Hepatogastroenterology 61:809–813
Chung YE, Kim MJ, Choi JY, et al. (2009) Differentiation of benign and malignant solid pseudopapillary neoplasms of the pancreas. J Comput Assist Tomogr 33:689–694
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All procedures performed in this study involving human participants were in accordance with the ethical standards of the institutional research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards. IRB approval was obtained, and informed consent was waved for this retrospective study.
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Takaji, R., Yamada, Y., Matsumoto, S. et al. Small pancreatic ductal carcinomas on triple-phase contrast-enhanced computed tomography: enhanced rims and the pathologic correlation. Abdom Radiol 43, 3374–3380 (2018). https://doi.org/10.1007/s00261-018-1645-6
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DOI: https://doi.org/10.1007/s00261-018-1645-6