Imaging presentation of pancreatic neuroendocrine neoplasms
Pancreatic neuroendocrine neoplasms (P-NENs) are the second most common solid pancreatic neoplasms. P-NENs have a wide range of imaging features presentations and they can be detected with typical and atypical imaging presentations. Typical and atypical appearances can be explained by pathologic correlations. P-NENs are generally hypervascular lesions, showing a typical enhancement behavior after contrast media injection during imaging methods, but they could also have different imaging features, creating some difficulty in differential diagnosis. For this reason, radiologists should be aware of different imaging presentations of these neoplasms. Radiological evaluation has a critical role in P-NENs identification, characterization, and staging of these neoplasms, especially in those cases in which surgery is the treatment of choice. The present paper shows, indicating the underlying pathologic correlations, typical and atypical presentations of NENs.
• P-NENs have a wide range of imaging features presentations, typical and atypical.
• Pathology could help in better understanding the typical P-NENs appearance at imaging.
• P-NENs are generally hypervascular lesions.
• Radiological evaluation has a critical role in P-NENs identification and management.
• Radiologists should know every type of different imaging presentation of P-NENs to better diagnose these kinds of lesions.
KeywordsPancreatic neuroendocrine tumors Pancreatic neuroendocrine neoplasms P-NEN
Pancreatic neuroendocrine neoplasm
Pancreatic neuroendocrine neoplasms (P-NENs) have a wide range of imaging features presentations. They can show different typical and atypical, common and uncommon, rare and very rare imaging presentations. Typical appearances can be explained by pathologic correlations and multimodalities approaches (US, CT, MRI, EUS, and PET) can be used to better show these features.
A radiologist has to know every possible imaging presentations range to improve the diagnosis and, therefore, management and treatment of P-NENs.
P-NENs are the second most common solid pancreatic neoplasms, after the first pancreatic ductal adenocarcinoma. Nevertheless, they are rare neoplasms, accounting for 1–2% of all pancreatic lesions . Even though they are rare tumors, in the last 20–30 years, their incidence has significantly increased more than twice, due to diagnostic imaging improvements and to medical knowledge increase [2, 3, 4]. Most of the time, they are sporadic tumors and they are solitary, whereas sometimes they are part of hereditary syndromes, such as multiple endocrine neoplasia type 1 (MEN1), Von Hippel–Lindau (VHL), neurofibromatosis type 1 (NF1), and tuberous sclerosis complex (TSC), and, in these hereditary syndromes, they present more frequently as multifocal lesions .
P-NENs can be divided into two categories, based on patients’ symptoms complained: functioning, if they produce and release hormones with different syndromes, depending on the produced molecule type, and non-functioning, in case of tumors inactivity. Non-functioning lesions are more frequent than functioning ones, accounting for two-thirds of all P-NENs [1, 2, 5, 6, 7]. However, in recent years, the small non-functioning lesions have been diagnosed incidentally with increased frequency in asymptomatic patients, due to imaging techniques improvements.
The tumor grade is one of the most important prognostic factors of neuroendocrine tumors, underlying the importance of knowing this data, by means of histological analysis. With increase of the tumor grade, the prognosis is lower.
NEN G1: Ki67 < 3% and/or < 2/10 mitosis 10/HPF; well differentiated
NEN G2: Ki67 > 3% and < 20% and/or 2–20 mitosis 10/HPF; well differentiated
NEN G3: Ki67 > 20% and/or > 20 mitosis 10/HPF; well differentiated
NEC (neuroendocrine carcinoma) G3 small cells: Ki67 > 20% and/or > 20 mitosis 10/HPF; poorly differentiated
NEC G3 large cells: Ki67 > 20% and/or > 20 mitosis 10/HPF; poorly differentiated
As previously stated, these neoplasms are mainly subdivided into two large groups (functioning and non-functioning), with different main features.
Functioning P-NENs are usually diagnosed in younger patients compared to the non-functioning P-NENs (55 years vs. 59 years), and the first type are usually smaller in dimension (< 3 cm) and usually non-metastatic at the time of diagnosis. However, the non-functioning neoplasms are generally the majority of P-NENs, accounting for about 40–90% of cases [2, 9]. Usually, functioning P-NENs present early with clinical manifestations related to the produced hormones, so, often, patients with P-NENs undergo imaging studies with a strong suspicion of disease.
The second most common type of functioning P-NENs are gastrinomas, accounting for about 20% of cases. Gastrinomas are slightly prevalent in middle-aged (V decade) men and they are usually located in the “gastrinoma triangle”, defined as the anatomical area among the junction of the cystic duct and common bile duct, the second and third duodenal portions, and the pancreatic head and neck. They tend to have a malignant course, accounting for about 60–65% of cases, and they are often multiple (about 60% cases, of which 20–60% in MEN1 disease) [1, 10].
Other histological types are somatostinomas, glucagonomas, ACTH-omas, and VIP-omas, accounting for a small percentage of P-NENs, about 20%, and their behavior can be atypical as a rule, so they tend to be bigger, malignant, and metastatic at diagnosis most of the time [1, 7, 10, 11, 12].
As previously stated, small non-functioning P-NENs are being incidentally discovered with increasing frequency in asymptomatic patients, due to recent advances in imaging methods and an increasing number of imaging abdominal scans and studies [1, 13, 14].
Typical imaging presentations
During imaging, P-NENs usually present as a solid hypervascular mass (Fig. 3).
During US, P-NENs are usually well-marginated hypoechoic masses with sharp margins, more or less homogeneous due to their size, which can vary. Doppler study could show small vessels within lesions. These neoplasms typically appear hypervascular (Fig. 3) during contrast-enhanced ultrasound (CEUS), and they usually show a rapid and intense enhancement in the early contrast-enhanced phase [1, 15, 16]. In bigger lesions, such as non-functioning types, necrotic intralesional areas can be seen within the rapid intense enhancement in the early dynamic phase at CEUS. Non-functioning P-NENs usually have a larger size than functioning P-NENs, which also justifies their tendency to contain necrosis and hemorrhage, giving them a typical presentation at imaging before and after contrast injection. Small calcifications, central necrotic or hemorrhagic, or cystic degeneration can be better identified during ultrasound harmonic imaging within P-NENs [1, 6, 17].
During CT, P-NENs typically present as more or less homogeneously isodense or slightly hypodense, well-defined masses during the pre-contrast phase, but they can also be inhomogeneous if larger. After contrast injection, during the arterial phase, they tend to be homogeneous or inhomogeneous hyperdense (Fig. 3), generally well depictable with respect to the adjacent parenchyma, and hyperdense or isodense during the portal phase, due to their vascularization. Very small intralesional calcifications can be presented in particular in the largest non-functioning lesions, which can also be inhomogeneous (Fig. 5), due to the presence of hypodense necrotic areas [1, 14, 18, 19, 20].
At MRI, they usually present as well-defined rounded lesions, homogeneously hypointense on T1-weighted sequence and hyperintense on T2-weighted sequence, better visualized with fat-suppression techniques. In case of bigger dimensions, they could be more inhomogeneous.
Diffusion-weighted imaging (DWI) may be useful in the study of P-NENs because, usually, they have clear restriction signal during DWI (Fig. 2) due to the high cellularity. DWI may help in the detection of P-NENS, especially for localizing non-hypervascular neoplasms . It has been reported that P-NENs with different grades of differentiation can be distinguished evaluating ADC maps: poor-differentiated P-NENs have significantly lower mean ADC values compared to normal pancreatic tissue and to well-differentiated pancreatic neuroendocrine tumors [22, 23, 24]. DWI MR could predict pancreatic neuroendocrine tumor grade, as reported in the literature, playing a role in tumor prognostic stratification at the beginning of the clinical history of the patient . After intravenous contrast administration, they typically appear hypervascular (Fig. 3) during the arterial phase and isointense or slightly hyperintense during the portal phase, more or less homogeneous related with their dimensions [1, 18, 19, 26].
Imaging methods can have a role in the detection, characterization, and staging of P-NENs. The staging of these tumors is important to choose the better treatment plan.
Metastases from P-NENs tend to resemble imaging features of primary tumors, usually showing enhancement after contrast media injection.
Atypical imaging presentations and variants
P-NENs could show atypical behavior. The most common atypical presentations are the hypoenhancing pattern, the intravessels growth, the intraductal growth, and the cystic and calcified variants .
In this variant, the involvement of the main pancreatic duct is more frequent, with also the presence of the “double-duct sign” if there is a concomitant involvement of the common bile duct due to a lesion occurring in the pancreatic head. This tumor variant at imaging is very close to the expected picture of a ductal adenocarcinoma, especially if it is small in dimension, implicating the cytological or histological confirmation mandatory in every case . At imaging, these fibrous P-NENs have atypical features, appearing hypovascular in the arterial phase at CT and MRI and with a possible progressive enhancement in the other phase due to the presence of fibrosis within lesions, except during CEUS due to the microbubble contrast media inner characteristics. Moreover, during MRI, it could lack the typical high hyperintensity on T2-weighted images, appearing isointense or slightly hyperintense on T2-weighted sequences, and, also, the strong restriction on DWI could be missed, causing mistakes in the differential diagnosis.
Intraductal location and growth of P-NENs may occur in two different scenarios. First, as part of a parenchymal pancreatic lesion strictly next to the main pancreatic duct that extends into the pancreatic duct and then grows along it, so the intraductal growth is connected to an extraductal lesion [1, 30, 31]. Second, the rarer setting of a NEN that originates within the main duct, fills the lumen as a polypoid mass, and grows along the duct. This type of lesion does not have a parenchymal component . Usually, this behavior is shown by non-functioning neoplasms that could grow within the main pancreatic duct and may completely obstruct the lumen, causing an obstructive pancreatitis.
The intraductal growth could be very insidious at imaging because it could be small in dimension and could be masked by pancreatitis signs. In case of an intraductal lesion associated with intrapancreatic lesion, at imaging, it could be possible to see the intrapancreatic one. Whereas in the case of a lesion that is exclusively intraductal, this is very difficult to observe at imaging; in the majority of these cases, diagnosis is possible only after surgery. At US, lesions may appear hyperechoic and difficult to separate from adjacent pancreatic parenchyma. At CT, often, these lesions are not visible. MR could be useful due to cholangiopancreatography (MRCP) because it could be possible to see a filling defect because lesions could appear hypointense compared to surrounding fluid and it could be possible to see them enhance following the administration of contrast agent.
In case of vessels involvement, this particular growing pattern is usually confined to peri-pancreatic vessels, such as splenic and portal veins, producing a neoplastic thrombus, characterized by enhancement during contrast media imaging studies, quite the opposite of blood clot thrombus .
P-NENs may also present as a lesion growing around the main pancreatic duct, causing abrupt-type stricture with upstream dilatation and a normal-caliber duct downstream of the stricture [1, 34, 35]. These neoplasms are usually positive using serotonin and very small in dimensions, exhibiting highly fibrotic stroma, and, as a consequence, poor vascularization.
In 5–10% of cases, P-NENs could present a cystic degeneration, usually in non-functioning lesions, causing some difficulties in differential diagnosis. Usually, cystic NENs are larger, more often symptomatic, and more likely to be non-functional than solid NENs .
During US, neuroendocrine cystic neoplasms are anechoic lesions delimited by a wall of variable thickness. In case of contrast media injection, this wall and eventual inner septa show enhancement.
During CT, usually, the cystic portion is hypodense, with wall and septa enhancement after contrast media injection.
CT is the most common initial imaging study in the evaluation of patients with cystic pancreatic lesions, whereas the gold standard in studying pancreatic cystic lesions is MR, due to its superior fluid and soft-tissue contrast, and it affords the best non-invasive means for the morphologic evaluation of cystic lesions of the pancreas. The MR signal is typically low in T1-weighted sequences, and high in T2-weighted sequences, with enhancement of wall and septa in post-contrastographic phases.
Calcifications may occur in P-NENs, unlike intra-tumor calcifications, which are not often seen in ductal adenocarcinoma. More commonly, calcifications occur within non-functioning and larger neoplasms [22, 38]. However, insulinoma may contain calcifications in up to 20% of cases. Overall, calcifications can be found in NENs in up to 16% of cases; these calcifications tend to be focal, coarse, irregular, and centrally located [22, 39].
Summary of typical and atypical aspects during imaging of pancreatic neuroendocrine neoplasms (P-NENs)
Well-marginated hypoechoic with sharp margins
Hypervascular with rapid and intense enhancement
Isodense or slightly hypodense, well-defined, hyperdense in arterial phase, hyperdense or isodense in portal phase
Well-defined, hypointense on T1W and hyperintense on T2W (better conspicuity in FAT-SAT)
Clear restriction signal at DWI
Hypervascular in arterial phase and isointense or slightly hyperintense in portal phase
Hypodense in arterial phase, possible enhancement in portal and late phases
Isointense or slightly hyperintense on T2-weighted sequences
No strong restriction at DWI
Hypointense in arterial phase, possible enhancement in portal and late phase
Hyperechoic areas with prominent posterior acoustic shadowing
Hyperdense areas with high HU values
Signal void artefact
Filling defect at MRCP
Possible enhancement after contrast media
Intravessel vascularized thrombus
Intravessel vascularized thrombus
Absence of flow void artefact
Intravessel vascularized thrombus
Anechoic lesion delimited by wall and possible inner septa
Hypervascular enhancement of wall and septa
Hypodense cystic portion
Hypervascular enhancement of wall and septa
Hypointense in T1W, hyperintense in T2W
Hypervascular enhancement of wall and septa
Nuclear medicine techniques
The majority of P-NENs (about 70%), with the exception of insulinomas and poorly differentiated neoplasms, are usually characterized by lots of somatostatin receptors (SSRs) along the cell membrane, and this is the reason why functional imaging with somatostatin analogs is able to clearly show these neoplasms [40, 41, 42].
Somatostatin receptor scintigraphy (SRS), also called OctreoScan due to the first commercially available somatostatin analog called Octreotide, is based on the high affinity of synthetic somatostatin analogs for tissue expressing SSRs, such as most NENs.
This technique gives a scan of the whole body, allowing the detection of primitive tumor and metastatic lesions. Moreover, SRS gives functional information based on SSRs expression by the tumor, also contributing to the correct selection patients’ therapy with somatostatin analogs and/or radiometabolic therapy [2, 43]. Nevertheless, SRS has the intrinsic limit of basing itself only on the tumor SSRs expression. Non-specific uptake in inflammatory tissue or normal organs and poor intrinsic spatial resolution are two recognized limitations of SRS. Often, poorly differentiated NENs and insulinomas are not identified during SRS, and it does not give anatomical or surgical resectability information [2, 44].
Fused positron emission tomography (PET)/computed tomography (CT) is a recent imaging technique that provides functional information for PET study and anatomic details for CT study. PET/CT provides help in depicting pancreatic tumors and distant metastases, in performing pre-operative staging, and in monitoring treatment response .
A new PET tracer, 68Ga-DOTATATE, a new somatostatin analog combined with gallium (with other somatostatin analogs labeled with gallium), was recently introduced to nuclear medicine in the NENs study, and several investigations showed that it has greater sensitivity than OctreoScan in detecting P-NENs, in particular the small ones [45, 46, 47]. As a consequence, PET with gallium could be used in tumor detection and staging, and in selecting the correct treatment and therapy for patients.
Another radiopharmaceutical used in PET imaging is fluorodeoxyglucose (FDG), because, usually, tumoral cells have high glucose metabolism, and, as a consequence, they show FDG uptake. Generally, well-differentiated, slow-growing NENs demonstrate little or no FDG uptake, due to their low metabolic activity, whereas poorly differentiated NENs and metastases from P-NENs, which rarely express somatostatin receptors, are well depicted during FDG-PET. For the depiction of P-NENs, FDG PET has a sensitivity of 53–57% [40, 41, 48, 49, 50]. For these reasons, FDG PET/CT can play a role in discerning well- and poor-differentiated neoplasms because, with the increase in aggression and malignancy potential of the tumor, there is an increase in the glucose uptake by the neoplasm. FDG activity on PET is related to tumor progression and increased mortality [45, 51, 52].
Kayani et al.  reported that high-grade and poor-differentiated NENs show greater FDG uptake, whereas low-grade and well-differentiated tumors demonstrate greater 68Ga-DOTATATE uptake.
Imaging methods, such as transabdominal ultrasound, endoscopic ultrasound, and CT, can also be used to guide fine needle aspiration or fine needle biopsy for cytological and/or histological confirmation of P-NENs.
Moreover, in NENs, interventional radiology could play an important role, especially in the control of non-surgical cases of disease.
Local treatment strategies such as embolization, chemoembolization, and targeted radionuclide therapy are increasingly being used in case of metastatic liver disease; moreover, local ablative techniques such as radiofrequency ablation (RFA) and cryotherapy are also important tools [53, 54].
P-NENs treatment should be individualized for every patient and planned by a multidisciplinary group.
The first treatment for P-NENs is radical surgery, and in patients with advance disease and/or metastatic disease, a multidisciplinary approach should be linked to surgical methods .
Surgery is the treatment of choice for both primary tumors and metastatic lesions if eradicable, and this is why differential diagnosis with pancreatic ductal adenocarcinoma is very important, due to the completely different treatment choice and consequent prognosis.
In case of functioning neoplasms, surgery should be mandatory due to the symptoms complained by patients, also in case of small lesions, whereas in case of small (< 2 cm) non-functioning neoplasms well differentiated and with a low grade, nowadays it is possible to use a “wait and watch” follow-up, in order to avoid mortality and surgery complications in patients with lesions with a very low malignancy rate.
In some cases, for example in local advanced disease, it should be useful to follow a “neoadjuvant therapy” with somatostatin analogs and/or metabolic radiotherapy to downstage the disease and then apply surgery.
In case of metastatic disease, there are several possibilities, such as chemotherapy, therapy with somatostatin analogs, metabolic radiotherapy, and local treatment, the latter with interventional radiology, such as RFA and trans-arterial chemoembolization.
Pancreatic neuroendocrine neoplasms (P-NENs) are typically hypervascular, but they could present with atypical features. At imaging, the atypical presentations of P-NENs are less frequent than typical presentations, but they could be very heterogeneous and hard to characterize, because of peculiar pathological changes, causing possible misdiagnosis. As a consequence, it is very important for radiologists to know all of the possible P-NENs presentations forms.
- 1.D’Onofrio M, Capelli P, Pederzoli P (eds) (2015) Imaging and pathology of pancreatic neoplasms. A pictorial atlas. Springer, MilanGoogle Scholar
- 5.Procacci C, Biasiutti C, Carbognin G et al (2001) Pancreatic neoplasms and tumor-like conditions. Eur Radiol 11(S2):S167–S192Google Scholar
- 11.Lee LS (2010) Diagnosis of pancreatic neuroendocrine tumors and the role of endoscopic ultrasound. Gastroenterol Hepatol (N Y) 6:520–522Google Scholar
- 34.Heller SJ, Ferrari AP, Carr-Locke DL, Lichtenstein DR, Van Dam J, Banks PA (1996) Pancreatic duct stricture caused by islet cell tumors. Am J Gastroenterol 91:147–149Google Scholar
Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.