eMedicine Specialties > Radiology > Gastrointestinal

Pseudocyst, Pancreatic: Imaging

Author: Michael AJ Sawyer, MD, Director, Videoendoscopic Surgical Institute of Oklahoma, Consulting Staff, Department of Surgery, Comanche County Memorial Hospital; Consulting Staff, Great Plains Surgical Clinic, Lawton, Oklahoma
Coauthor(s): Manish K Varma, MD, Chief of Interventional Radiology, Department of Radiology, Tripler Army Medical Center
Contributor Information and Disclosures

Updated: Aug 30, 2007

Radiography

Findings

Plain radiographs are not a typical choice in the diagnostic armamentarium for pancreatic pseudocysts. These images may be obtained in patients undergoing a workup for nonspecific abdominal pain.

If the patient has a pancreatic pseudocyst, plain abdominal radiographs may depict its presence on the basis of the mass effect caused by the pseudocyst. In this case, findings include suggestion of a soft-tissue mass displacing or compressing surrounding hollow viscera such as the stomach, duodenum, or transverse colon. Other diagnostic clues to the condition can include the presence of calcifications in the pancreatic duct in a patient with chronic pancreatitis.

Degree of Confidence

Although plain radiographs can demonstrate soft-tissue mass effect, findings are nonspecific and must be confirmed by using other diagnostic modalities. The studies of choice include abdominal CT scanning and abdominal US.

False Positives/Negatives

Other cystic lesions of the pancreas may be misinterpreted as pancreatic pseudocysts. No normal anatomic variants mimic a pseudocyst.

Computed Tomography

Findings

Abdominal CT is an excellent choice for imaging acute fluid collections and pancreatic pseudocysts. Most patients with clinically significant pancreatitis undergo CT scanning. Contrast-enhanced dynamic CT scans are instrumental in determining the severity of pancreatitis (percentage of pancreatic necrosis). Therefore, they have become important predictors of the clinical course and prognosis.

Approximately 30-50% of patients presenting with acute pancreatitis have an associated acute fluid collection according to the work of Siegelman and colleagues9 and Bradley and coworkers.10 The fluid collections are found in the lesser omental sac; in other peripancreatic locations; or, occasionally, within the gland.

CT characteristics of an acute fluid collection include low attenuation and a homogeneous appearance. Occasionally, especially when associated with severe acute pancreatitis, CT attenuation values may be greater than 20-30 HU (Hounsfield units) because of the presence of necrotic pancreatic or peripancreatic debris or blood within the confines of the acute fluid collection. The presence of such material in the pseudocyst can make its appearance more heterogeneous on CT scans.

Pancreatic pseudocysts have several features that help distinguish them from acute fluid collections on CT scans. Most prominent is the presence of a well-defined, nonepithelial, fibrous wall around the pseudocyst. The wall is the result of the intense inflammatory response associated with pancreatitis and the spillage of enzyme-rich pancreatic juice into the peripancreatic tissues.

Pseudocysts are round or ovoid in configuration, whereas acute fluid collections are not well defined. A thick pseudocyst capsule may enhance with the addition of contrast. Bradley has described a time course of at least 4 weeks before an acute fluid collection matures into a pseudocyst, which occurs in as many as 50% of patients with an acute fluid collection.10,4

Degree of Confidence

The identification of a thick-walled, rounded, fluid-filled mass adjacent to the pancreas on an abdominal CT scan in a patient with a history of acute or chronic pancreatitis is virtually pathognomonic for pancreatic pseudocyst. Positive CT findings in this clinical situation do not require confirmation with another diagnostic modality.

Both abdominal CT scanning and US are highly sensitive and specific for the diagnosis of a pancreatic pseudocyst. In the acute setting, a CT scan is the better choice because significant amounts of bowel gas resulting from ileus or obstruction decrease the sensitivity of US. In addition, CT scans provide more detailed information regarding the surrounding anatomy and can demonstrate additional pathology, including pancreatic duct dilatation and calcifications, common bile duct dilatation, and extension of the pseudocyst outside the lesser sac.

False Positives/Negatives

The major weakness of CT scanning is the relative inability to distinguish pseudocyst from cystic neoplasms, especially mucinous cystadenomas and intraductal papillary mucinous tumors (IPMT). As Cooperman stated, the clinical history provides clues to a diagnosis other than pancreatic pseudocyst.6 If the patient has had no prior history of pancreatitis but has a cystic mass associated with the pancreas, an alternative diagnosis should be entertained.

Magnetic Resonance Imaging

Findings

Magnetic resonance imaging (MRI) and magnetic resonance cholangiopancreatography (MRCP) are sensitive diagnostic modalities for pancreatic pseudocysts. They are generally not routinely used because CT scanning typically offers all the diagnostic information that is required. However, the increased contrast provides for better characterization of fluid collections. MRI or MRCP is superior to CT in depicting debris within fluid collections and pseudocysts, as described by Chalmers11 and by Morgan and coworkers.12

On T2-weighted images, a fluid-filled cystic mass produces high signal intensity and appears bright on images. The pancreatic duct and biliary systems are easily visualized in detail, although interpreting the status of pancreatic duct integrity is difficult.

Degree of Confidence

As with CT scanning, the detection of a cystic mass in the proper clinical context should make the examiner confident that a pancreatic pseudocyst is present.

Although MRI is more expensive than CT, it has multiplanar capabilities, it requires no ionizing radiation, and it involves non-nephrotoxic contrast agents. Its ability to depict choledocholithiasis is far superior to that of CT or US. Furthermore, MRCP techniques can also depict subtle branch-chain dilatation in chronic pancreatitis. They are also highly sensitive to blood products such as that seen in complex hemorrhagic fluid collections or pseudocysts.

False Positives/Negatives

Megibow and coworkers13 and Dani and colleagues14 have stated that MRI offers no advantage over CT scanning in the differentiation of pancreatic pseudocysts from other pancreatic cystic lesions. The patient's clinical history is extremely important in this situation.

Ultrasonography

Findings

Pancreatic pseudocysts appear as anechoic structures associated with acoustic enhancement on US examination. They are well defined and round or oval, and they are contained within a smooth wall.

During the early phases of their development, pseudocysts can appear more complex, with varying degrees of internal echoes. Usually, this appearance results from the presence of necrotic pancreatic and peripancreatic debris and is more common in pseudocysts that form as a result of acute necrotizing pancreatitis than in other pseudocysts. The debris is cleared over time. The pseudocyst can appear more complex in 2 other instances: when hemorrhage occurs into the cyst or when infection of the cyst complicates the clinical course.

Color Doppler or duplex scanning should always be performed in cystic lesions to ensure that the lesion in question is not a giant pseudoaneurysm.

Degree of Confidence

Sensitivity rates for US in the detection of pancreatic pseudocysts are 75-90%, according to Pitchumoni and Agarwal15 ; therefore, US is slightly inferior to CT, which has a sensitivity of 90-100%.

US has several limitations, as compared with CT, in the initial diagnosis of a pseudocyst: the presence of overlying bowel gas decreases the sensitivity of US, and unlike CT, US examinations are highly operator dependent. However, CT scans provide more information regarding the surrounding viscera and vasculature.

False Positives/Negatives

No normal anatomic variants mimic the presence of a pseudocyst; however, other cystic pancreatic masses can be misinterpreted as pseudocysts. This observation is important because as many as 10% of cystic pancreatic lesions are neoplasms; examples of these include serous and mucinous cystadenomas and mucinous cystadenocarcinomas. Clues to the diagnosis of a neoplastic cyst include a complex nature and the presence of internal septations, which can be extremely difficult to detect with US.

Brugge states that endoscopic US is helpful in the differentiation of pancreatic fluid collections.16 Endoscopic US is more sensitive than transcutaneous US for demonstrating the internal architecture of the lesions.

Nuclear Imaging

Findings

Radionuclide examinations are rarely used for the diagnosis of pancreatic pseudocysts. Nevertheless, they can depict the presence of a pseudocyst, which appears as a photon-deficient mass in proximity to the pancreas. Tracers used in the diagnosis of a pancreatic pseudocyst include gallium-67 citrate and selenium-75 selenomethionine.

Pseudocysts can also be demonstrated scintigraphically if they dissect into the spleen, where they can be associated with subcapsular splenic hemorrhage. In these instances, case reports have been published in which a pseudocyst was imaged as a splenic defect on scanning using technetium-99m sulfur colloid.

Degree of Confidence

Nuclear medicine scans must be considered a poor choice in the diagnosis of pancreatic pseudocysts. They depend on indirect information such as compression or invasion of surrounding structures. The information they provide can demonstrate a mass effect but is nonspecific in aiding with an exact diagnosis.

If the presence of a pseudocyst is suggested on the basis of the results of a nuclear medicine study, the diagnosis must be confirmed by means of a more accurate examination such as abdominal CT or abdominal US. These studies are highly accurate in the diagnosis of a pancreatic pseudocyst.

False Positives/Negatives

No specific conditions cause false-negative or false-positive findings on nuclear medicine scans.

Angiography

Findings

Angiography is rarely, if ever, useful in the diagnosis of pancreatic pseudocysts. Arterial pseudoaneurysms resulting from vessel erosion by pancreatic pseudocysts and acute pancreatitis are another matter. In these conditions, angiography can be used as both a diagnostic technique and a therapeutic modality.

Expectant management of pancreatic pseudocysts, including observation and waiting for their resolution, has been associated with rates of significant hemorrhage as high as 18%, according to a report by Kiviluoto and coworkers.17 Angiographic intervention has been helpful in controlling such hemorrhage. In addition, interventional angiographic techniques have been instrumental in decreasing the mortality rate associated with hemorrhagic complications of acute pancreatitis by transcatheter embolization of bleeding vessels and pseudoaneurysms.

Degree of Confidence

For diagnostic purposes, angiography is not a good choice because it is invasive, it exposes the patient to contrast material, and it offers no advantages over CT, MRI, or US.

False Positives/Negatives

To the authors' knowledge, no comprehensive discussions describe the issue of false-positive or false-negative angiographic findings related to pancreatic pseudocysts.

More on Pseudocyst, Pancreatic

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Imaging: Pseudocyst, Pancreatic
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Multimedia: Pseudocyst, Pancreatic
References

References

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Further Reading

Keywords

lesser sac fluid collection, acute fluid collection, internal pancreatic fistula, postnecrotic pseudocysts, retention cysts, pancreatic cysts, postnecrotic pseudocysts

Contributor Information and Disclosures

Author

Michael AJ Sawyer, MD, Director, Videoendoscopic Surgical Institute of Oklahoma, Consulting Staff, Department of Surgery, Comanche County Memorial Hospital; Consulting Staff, Great Plains Surgical Clinic, Lawton, Oklahoma
Michael AJ Sawyer, MD is a member of the following medical societies: American College of Surgeons, Society for Surgery of the Alimentary Tract, Society of American Gastrointestinal and Endoscopic Surgeons, and Society of Laparoendoscopic Surgeons
Disclosure: Nothing to disclose.

Coauthor(s)

Manish K Varma, MD, Chief of Interventional Radiology, Department of Radiology, Tripler Army Medical Center
Manish K Varma, MD is a member of the following medical societies: American College of Radiology, American Roentgen Ray Society, and Radiological Society of North America
Disclosure: Nothing to disclose.

Medical Editor

Glenn Krinsky, MD, Chief of Abdominal Imaging Section, Associate Professor, Department of Radiology, New York University School of Medicine
Glenn Krinsky, MD is a member of the following medical societies: Alpha Omega Alpha and Radiological Society of North America
Disclosure: Nothing to disclose.

Pharmacy Editor

Bernard D Coombs, MB, ChB, PhD, Consulting Staff, Department of Specialist Rehabilitation Services, Hutt Valley District Health Board, New Zealand
Disclosure: Nothing to disclose.

Managing Editor

Udo P Schmiedl, MD, PhD, Clinical Professor, Department of Radiology, University of Washington; Consulting Staff, Swedish Medical Center, University of Washington Medical Center, Seattle Radiologists
Udo P Schmiedl, MD, PhD is a member of the following medical societies: American College of Radiology and Radiological Society of North America
Disclosure: Nothing to disclose.

CME Editor

Robert M Krasny, MD, Consulting Staff, Department of Radiology, The Angeles Clinic and Research Institute
Robert M Krasny, MD is a member of the following medical societies: American Roentgen Ray Society and Radiological Society of North America
Disclosure: Nothing to disclose.

Chief Editor

Eugene C Lin, MD, Consulting Staff, Department of Radiology, Virginia Mason Medical Center
Eugene C Lin, MD is a member of the following medical societies: American College of Nuclear Medicine, American College of Radiology, Radiological Society of North America, and Society of Nuclear Medicine
Disclosure: Nothing to disclose.

 
 
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