Abstract

BackgroundThe aim is to assess the time-density curves (TDCs) and correlate the histologic results for small (≤ 2 cm) PDA and surrounding parenchyma at triphasic Multidetector-row CT (MDCT).MethodsTriphasic MDCT scans of 38 consecutive patients who underwent surgery for a small PDA were retrospectively reviewed. The TDCs were analyzed and compared with histologic examination of the PDA and pancreas upstream/downstream in all cases. Three enhancement patterns were identified: 1) enhancement peak during pancreatic parenchymal phase (PPP) followed by a rapid decline on portal venous phase (PVP) and delayed phase (DP) at 5 minutes (type 1 pattern: normal pancreas); 2) maximum enhancement in PVP that gradually decreases in DP (type 2 pattern: mild chronic pancreatitis or PDA with mild fibrous stroma); 3) progressive enhancement with maximum peak in DP (type 3 pattern: severe chronic pancreatitis or PDA with severe fibrous stroma). A p value less than 0.05 was considered statistically significant. Sensitivity was calculated for PDA detection and an attenuation difference with the surrounding tissue of at least 10 HU was considered.ResultsPDA showed type 2 pattern in 5/38 cases (13.2%) and type 3 pattern in 33/38 cases (86,8%). Pancreas upstream to the tumor had type 2 pattern in 20/38 cases (52,6%) and type 3 pattern in 18/38 cases (47,4%). Pancreas downstream to the tumor had type 1 pattern in 19/25 cases (76%) and type 2 pattern in 6/25 cases (24%). Attenuation difference between tumor and parenchyma upstream was higher of 10 UH on PPP in 31/38 patients (sensitivity = 81.6%), on PVP in 29/38 (sensitivity = 76.3%) and on DP in 17/38 (sensitivity = 44.7%). Attenuation difference between tumor and parenchyma downstream was higher of 10 UH on PPP in 25/25 patients (sensitivity = 100%), on PVP in 22/25 (sensitivity = 88%) and on DP in 20/25 (sensitivity = 80%). Small PDAs were isodense to the pancreas upstream to the tumor, and therefore unrecognizable, in 8 cases (8/38; 21%) at qualitative analysis and in 4 cases (4/38; 10,5%) at quantitative analysis.ConclusionsThe quantitative analysis increases the sensitivity for detection of small PDA at triphasic MDCT.

Highlights

  • The aim is to assess the time-density curves (TDCs) and correlate the histologic results for small (≤ 2 cm) pancreatic ductal adenocarcinoma (PDA) and surrounding parenchyma at triphasic Multidetector-row Computed Tomography (CT) (MDCT)

  • On qualitative triphasic CT analysis, small PDAs were isodense to the pancreas upstream to the tumor in 8 cases (8/38; 21%); on delayed phase (DP) were detected 2 PDAs isoattenuating on pancreatic parenchymal phase (PPP) and portal venous phase (PVP)

  • Tumor shows progressive enhancement throughout the three phases with maximum peak in DP; pancreatic parenchyma upstream to the tumor shows maximum enhancement in PVP that gradually decreases in DP; pancreatic parenchyma downstream to the tumor shows maximum enhancement peak during PPP followed by a rapid decline on PVP and DP

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Summary

Introduction

The aim is to assess the time-density curves (TDCs) and correlate the histologic results for small (≤ 2 cm) PDA and surrounding parenchyma at triphasic Multidetector-row CT (MDCT). A similar degree of fibrosis in the tumor and surrounding pancreatic parenchyma, resulting in the form of mild or severe chronic obstructive pancreatitis, may determine a similar enhancement on MDCT precluding the identification of PDA. The knowledge by triphasic MDCT of the different enhancement patterns of PDA, pancreatic parenchyma upstream (toward the tail) and downstream (toward the head) to the tumor and histopathological features related are essential to increase the sensitivity of MDCT in the detection of PDA. Our aim is to correlate the time-density curves (TDCs) at triphasic MDCT with histological characteristics for small (≤ 2 cm) PDA and surrounding parenchyma

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