This document discusses the imaging findings and differential diagnosis of pancreatic cystic lesions, specifically distinguishing pancreatic pseudocysts from cystic neoplasms. Key points include:
- Pancreatic pseudocysts are the most common cystic pancreatic lesion and appear as fluid collections with thin walls that develop after pancreatitis.
- Cystic neoplasms, while less common, include lesions like serous cystadenomas that have characteristic honeycomb appearances due to numerous small cysts.
- Differentiating pseudocysts from cystic neoplasms is important for determining appropriate treatment and management of the cystic lesion.
This document discusses the imaging findings and differential diagnosis of pancreatic cystic lesions, specifically distinguishing pancreatic pseudocysts from cystic neoplasms. Key points include:
- Pancreatic pseudocysts are the most common cystic pancreatic lesion and appear as fluid collections with thin walls that develop after pancreatitis.
- Cystic neoplasms, while less common, include lesions like serous cystadenomas that have characteristic honeycomb appearances due to numerous small cysts.
- Differentiating pseudocysts from cystic neoplasms is important for determining appropriate treatment and management of the cystic lesion.
This document discusses the imaging findings and differential diagnosis of pancreatic cystic lesions, specifically distinguishing pancreatic pseudocysts from cystic neoplasms. Key points include:
- Pancreatic pseudocysts are the most common cystic pancreatic lesion and appear as fluid collections with thin walls that develop after pancreatitis.
- Cystic neoplasms, while less common, include lesions like serous cystadenomas that have characteristic honeycomb appearances due to numerous small cysts.
- Differentiating pseudocysts from cystic neoplasms is important for determining appropriate treatment and management of the cystic lesion.
The spectrum of imaging findings of cystic pancreatic
lesions and highlight the roles, advantages, and limitations of various imaging modalities in the differential diagnosis of pancreatic cystic lesions, with particular emphasis on pseudocysts versus nonpseudocysts LEARNING OBJECTIVES Identify the radiologic findings of pancreatic pseudocysts. Describe the radiologic findings of cystic pancreatic neoplasms. Discuss the findings that allow differential diagnosis between pancreatic pseudocysts and cystic pancreatic neoplasms. Pancreatic Pseudocyst Pseudocysts are the most common cystic lesions of the pancreas. wide application of computed tomography (CT) and ultrasound (US) in asymptomatic and mildly symptomatic patients has increased detection of incidental cystic lesions of the pancreas so that the differential diagnosis of pancreatic cystic lesions has become more challenging. Differentiating pancreatic pseudocysts from nonpseudocysts is important for determining treatment. Radiologic imaging alone has limited accuracy in differentiating between pseudocysts and nonpseudocysts due to similarities in the imaging findings of the lesions Thin-section CT and magnetic resonance (MR) cholangiopancreatography have gained popularity for the potential advantages of visualizing communication between the main pancreatic duct and a cystic lesion noninvasively. Endoscopic US has emerged as a modality that can provide anatomic structure in greater detail and facilitate aspiration biopsy of smaller lesions. When radiologic imaging findings and results of cyst fluid analysis with or without biopsy are interpreted in conjunction with a careful patient history, diagnostic accuracy may be increased substantially. Most cystic masses of the pancreas encountered in clinical practice are postinflammatory pseudocysts Pancreatic pseudocysts are defined as “localized amylase- rich fluid collections located within the pancreatic tissue or adjacent to the pancreas and surrounded by a fibrous wall that does not possess an epithelial lining.” The CT findings of a pseudocyst include a round or oval fluid collection with a thin, barely perceptible wall or thick wall that shows evidence of contrast enhancement. They develop most often as a complication of acute or chronic pancreatitis and may develop secondary to pancreatic trauma or surgery Clinical scenarios pseudocyst developing after identifiable acute pancreatitis a pseudocyst resulting from an acute incident superimposed on chronic pancreatitis pseudocyst with an uncertain or no known previous clinical history of pancreatitis. Classic Postinflammatory Pancreatic Pseudocyst After an acute attack, the pseudocyst develops during a period of 4–6 weeks. Pseudocysts may be followed conservatively if they are smaller than 6 cm in diameter or the patient is asymptomatic because pseudocysts can resolve spontaneously Unilocular pseudocysts occur more frequently than multilocular pseudocysts. Complications related to pseudocysts include infection, hemorrhage, rupture, and obstruction of other abdominal organs. Secondary infection of the pseudocyst is a dreaded complication due to its high rate of morbidity and mortality, requiring drainage by radiologic, endoscopic, or surgical decompression Figure 1a. Developing pseudocyst in a 63-year-old woman with epigastric pain. (a) Unenhanced CT scan shows an edematous pancreas and an ill-defined, acute fluid collection surrounding the tail of the pancreas (arrow) with peripancreatic inflammatory changes, an appearance compatible with acute pancreatitis Figure 1b. Developing pseudocyst in a 63-year-old woman with epigastric pain. On a follow-up contrast-enhanced CT scan obtained 1 month later, the lesion appears as a bilobed cystic mass with a septum in the pancreatic body and tail (arrow). The peripancreatic inflammatory changes are markedly decreased. Figure 1c. Developing pseudocyst in a 63-year-old woman with epigastric pain. On a follow-up CT scan obtained 2 years later, the lesion appears as a unilocular, low- attenuation fluid collection with a well-defined thin wall (arrow). This is the typical appearance of a postinflammatory pseudocyst. Figure 2a. Progressive evolution and spontaneous resolution of a pancreatic pseudocyst in a 31-year-old man with left upper quadrant pain. (a) Initial contrast-enhanced CT scan shows an edematous pancreas and peripancreatic inflammatory changes, an appearance compatible with acute pancreatitis Figure 2b. Progressive evolution and spontaneous resolution of a pancreatic pseudocyst in a 31-year-old man with left upper quadrant pain. Follow-up CT scan obtained 2 months later shows a relatively thick-walled cyst in the pancreatic tail (arrow). This lesion represents a maturing pseudocyst. Figure 2c. Progressive evolution and spontaneous resolution of a pancreatic pseudocyst in a 31-year-old man with left upper quadrant pain. CT scan obtained 4 months later shows resolution of the pseudocyst. Pancreatic Pseudocyst Superimposed on Chronic Pancreatitis Pancreatic pseudocysts can occur in association with chronic pancreatitis as chronic pseudocysts or can result from acute exacerbation of pancreatitis or chronic pancreatitis. In the former case, a distinct clinical history of acute pancreatitis may be lacking and the pseudocyst is often detected incidentally, in comparison with the latter case. The recognition of a pancreatic pseudocyst resulting from chronic pancreatitis is usually easy when there are associated stigmata of chronic pancreatitis such as parenchymal calcifications or ductal stones, ductal dilatation, and atrophy of the parenchyma (Fig 5). Figure 5a. Chronic pancreatitis with an intrapancreatic pseudocyst in a 42-year-old man with a history of alcoholic pancreatitis. (a) Contrast- enhanced CT scan shows a dilated pancreatic duct (arrows) with mild pancreatic atrophy, an appearance compatible with chronic pancreatitis Figure 5b. Chronic pancreatitis with an intrapancreatic pseudocyst in a 42-year-old man with a history of alcoholic pancreatitis. a round mass with diffuse low attenuation in the pancreatic head (curved arrow). The mass represents a pseudocyst. Note the dilated pancreatic duct (straight arrow). Figure 5c. Chronic pancreatitis with an intrapancreatic pseudocyst in a 42-year-old man with a history of alcoholic pancreatitis.. (c) Contrast- enhanced CT scan shows pancreatic calcifications (arrow), a finding compatible with chronic pancreatitis. Pancreatic Pseudo-cyst without an Antecedent Episode of Acute Pancreatitis Incidental pancreatic cysts are smaller than symptomatic cysts and are unlikely to be pseudocysts. Cystic pancreatic neoplasm should be considered in the differential diagnosis of a pancreatic cyst, even in patients with a history of pancreatitis, if no recent episode of acute pancreatitis can be documented on clinical or imaging grounds. For pancreatic pseudocysts without an antecedent episode of acute pancreatitis and radiologic evidence of pancreatitis, US-, CT-, or endoscopic US–guided aspiration or biopsy or at least a follow-up study should be recommended. Figure 4. Hemorrhagic pseudocyst in a 45-year-old man who experienced an episode of abdominal pain but had no clinical findings suggestive of infection. Contrast-enhanced CT scan shows a cystic mass containing an area of high attenuation (arrow), a finding consistent with recent hemorrhage. Figure 6a. Incidentally detected pancreatic pseudocyst in a 77-year-old woman with no known history of pancreatitis. (a) Image obtained with thin- section (2.5-mm section thickness) contrast-enhanced multidetector CT shows an ovoid hypoattenuating mass without internal septa or mural nodules in the pancreatic tail (arrow). Cystic Neoplasms uncommon increasingly being detected and are difficult to distinguish from pseudocysts, which are encountered far more frequently. D/d serous cystadenoma mucinous cystic neoplasm IPMT solid and papillary epithelial neoplasm (SPEN) and cystic islet cell tumor the average size of detected lesions has steadily decreased and imaging characterization becomes more difficult for smaller lesions. Serous Cystadenoma also referred to as microcystic cystadenoma typically found in women over the age of 60 years with nonspecific complaints of abdominal pain or weight loss or more commonly as an incidental finding. multiple cysts varying in size from 0.2 to 2.0 cm, and the size of the tumors ranges in greatest dimension from 1.4 to 27 cm A central stellate scar with calcification, which is known to be characteristic of serous cystadenoma, may sometimes be observed Continue… Internally, the cyst has a honeycombed appearance compatible with innumerable cysts. At US, the lesion may appear as a solid echogenic mass due to interfaces produced by the numerous cysts. It may appear as a solid mass at CT, depending on the size of the cysts and the amount of fibrous tissue Asymptomatic serous cystadenomas do not require surgical excision because they are rarely malignant. Tumors smaller than 2 cm have been reported and are more likely to be serous cystadenomas Macrocystic or oligocystic serous cystadenoma is a variant of serous cystadenoma that is very difficult to differentiate from mucinous cystadenoma Figure 7a. Serous cystadenoma in a 45-year-old woman with right upper quadrant pain. (a) Contrast-enhanced CT scan shows a low-attenuation mass with a honeycomb appearance in the pancreatic head and uncinate process (arrow). The honeycomb appearance is produced by numerous tiny cystic structures Figure 7b. Serous cystadenoma in a 45-year-old woman with right upper quadrant pain. (b) US scan shows that the mass has low echogenicity due to the interfaces between the tiny cysts. Note the increased through transmission posterior to the mass Figure 7c. Serous cystadenoma in a 45-year-old woman with right upper quadrant pain. Photograph of the cut surface of the specimen shows innumerable cysts. Location in the pancreatic head, lobulated contour, and lack of wall enhancement have been reported to be specific for macrocystic serous cystadenoma in comparison with mucinous cystic tumor. Lobulated contours have been reported to be a specific finding in comparison with pseudocyst. Oligocystic serous cystadenoma in a 56-year-old woman with epigastric pain. (a, b) US scan (a) and CT scan (b) show a well-demarcated cystic mass with peripheral internal septa (arrow) in the pancreatic head. Note the peripheral septum with calcification (arrow in b) Figure 9b. Oligocystic serous cystadenoma in a 56-year-old woman with epigastric pain. (a, b) US scan (a) and CT scan (b) show a well-demarcated cystic mass with peripheral internal septa (arrow) in the pancreatic head. Note the peripheral septum with calcification (arrow in b) Figure 9c. Oligocystic serous cystadenoma in a 56-year-old woman with epigastric pain. (c) Endoscopic pancreatogram shows the pancreatic duct splayed by the tumor. No communication exists between the lesion and the main duct Mucinous Cystic Neoplasms most common cystic tumors of the pancreas large cystic spaces are lined by tall, mucin- producing columnar cells. Mucinous cystic neoplasms may be unilocular or mutilocular and are commonly detected only after achieving a large size. Solid papillary excrescences sometimes protrude from the wall into the interior of these tumors. The absence of excrescences does not exclude malignancy. Figure 10. Incidentally detected mucinous cystadenoma in a 67-year-old woman. Contrast-enhanced CT scan shows a complex cystic mass with a few septa in the pancreatic tail (arrow). Figure 11. Mucinous cystadenoma in a 47-year-old woman with left upper quadrant pain. Contrast-enhanced CT scan shows a large cystic tumor with small cysts clustered at its periphery (arrow). . Multiple enhancing septations and solid intramural nodules are typical radiologic findings of mucinous cystic neoplasms Peripheral calcification, which can be seen in 10%–25%, is an important characteristic for mucinous cystic neoplasms and can be used to differentiate them from serous cystadenomas, which are known to have central calcification. Endoscopic US can depict the internal architecture of the cystic mass, including internal septa and tiny solid components, better than conventional CT, depending on the location of the tumor and patient body habitus. tumors are round to oval with a smooth external surface. Secondary cysts along the internal wall are common. Occasionally, communication between the pancreatic duct and the cystic neoplasm is present. Mucinous cystic tumors should always be resected because they are all potentially malignant. When the cyst is small in an asymptomatic patient, cyst aspiration and analysis of the cyst fluid can be helpful in differential diagnosis Mucinous Cystic Neoplasm Misdiagnosed as a Pseudocyst Owing to partial volume averaging with the hypoattenuating cyst fluid, the fine internal septa and small intramural nodules may not be visible at conventional contrast-enhanced CT. This explains why mucinous cystic neoplasm sometimes is misdiagnosed as a pseudocyst So to avoid this better is to use multidetector CT Figure 12. Mucinous cystadenocarcinoma in a 52-year-old woman with epigastric pain. Despite the absence of a history of pancreatitis, the thin cyst wall led to the presumptive diagnosis of a pseudocyst. CT scan shows a thin-walled cyst in the pancreatic tail. There is a tiny peripheral intramural nodular structure (arrow), which was initially overlooked. At surgery, the lesion proved to be a mucinous cystadenocarcinoma. Figure 13a. Incidentally detected mucinous cystadenoma in a 65-year-old woman. (a) Contrast-enhanced CT scan shows an ovoid hypoattenuating mass with barely visible septa in the pancreatic head (arrow). (b) Endoscopic US scan shows the complex cystic mass with multiple internal septa (arrow). Endoscopic US–guided fine-needle aspiration was performed, and cytologic analysis revealed abundant mucin with scant glandular epithelial cells, findings suggestive of a mucin- producing tumor. At surgery, the lesion proved to be a mucinous cystadenoma. Figure 13b. Incidentally detected mucinous cystadenoma in a 65-year-old woman. (a) Contrast-enhanced CT scan shows an ovoid hypoattenuating mass with barely visible septa in the pancreatic head (arrow). (b) Endoscopic US scan shows the complex cystic mass with multiple internal septa (arrow). Endoscopic US–guided fine-needle aspiration was performed, and cytologic analysis revealed abundant mucin with scant glandular epithelial cells, findings suggestive of a mucin-producing tumor. At surgery, the lesion proved to be a mucinous cystadenoma. Intraductal Papillary Mucinous Tumor IPMT is characterized by the papillary proliferation of pancreatic ductal epithelium and production of mucin. It is characterized by cystic dilatation of a main or a side branch duct that contains thick mucoid secretions. Patients present with nonspecific abdominal symptoms and sometimes hyperamylasemia. typically occur in elderly patients and are more common in men. Although the incidence of IPMT seems to be increasing, the likely explanation is increased use of imaging and awareness of this disease entity. IPMTs are classified into:- main duct type branch duct type and combined type. Accordingly, imaging findings vary depending on the type of the tumor.. The side branch duct type is the most commonly mistaken for mucinous cystic tumor or pseudocyst. Typical location (uncinate process), typical appearance (grapelike locular appearance), and communication with the duct at endoscopic retrograde cholangiopancreatography (ERCP) usually separate it from other lesions in the pancreas. A markedly dilated uncinate branch filled with mucus is a typical feature of a side branch IPMT ERCP is regarded as the modality of choice in the diagnosis of IPMT for its ability to depict the bulging ampulla of Vater, mucin pouring from the papilla, and communication between the pancreatic duct and the cyst cavity. Communication between the duct and the abnormal cystic structure can be shown with thin-section helical CT or with MR imaging and MR cholangiopancreatography. Although the classic diagnostic role of ERCP has been challenged to some extent by combined use of MR cholangiopancreatography and endoscopic US in the evaluation of IPMT, ERCP has a distinctive diagnostic role where the diagnosis is not clear on cross-sectional images. Figure 14a. Multiple branch duct type of IPMT. (a) Contrast-enhanced CT scan shows multiple cystic masses (straight arrow) in the pancreatic head and body. Note the dilated pancreatic duct (curved arrow) Figure 14b. Multiple branch duct type of IPMT. (a) Contrast-enhanced CT scan shows multiple cystic masses (straight arrow) in the pancreatic head and body. Note the dilated pancreatic duct (curved arrow). (b) Curved coronal reformatted view obtained along the pancreatic tail shows a communication between a cystic mass and the dilated distal pancreatic duct (arrow). Solid and Papillary Epithelial Neoplasm are histologically distinctive neoplasms of low malignant potential with a favorable prognosis. SPEN is typically found in young women. Most patients present with nonspecific signs and symptoms including nausea, vomiting, and abdominal pain or fullness. The tumor tends to be a large, well-circumscribed, and slowly growing mass. The tumor may have a variety of internal appearances, from purely cystic to completely solid, but is usually surrounded by a thick, well-defined rim. The appearance of the internal architecture typically depends on the degree of hemorrhage and necrosis of the tumor. Figure 17a. SPEN in a 32-year-old woman with epigastric pain. (a) Contrast-enhanced CT scan shows a mixed solid and cystic mass in the pancreatic head (arrows). Figure 17b. SPEN in a 32-year-old woman with epigastric pain. (b) Axial T1-weighted MR image (500/20) shows areas of high signal intensity due to hemorrhage within the mass (arrow). Multidetector CT and MR Imaging with MR Cholangiopancreatography The improved multiplanar capability, thin collimation, and ability to optimize parenchymal enhancement of multidetector CT not only improve the detection rate of the cystic pancreatic lesion but may enhance diagnostic accuracy by depicting fine internal architecture and the anatomic relationship between the main pancreatic duct and the cystic lesions Image-guided Fine-Needle Aspiration Biopsy can be obtained by conventional US- or CT-guided percutaneous needle aspiration or by an endoscopic US–guided technique. Analysis of the cystic contents includes viscosity, enzymes (amylase, lipase), tumor markers (carcinoembryonic antigen [CEA], cancer antigen 19-9 [CA 19-9]), and cytologic findings, which may help differentiate between neoplastic cysts and pseudocysts. Endoscopic US and US-guided Fine-Needle Aspiration or Biopsy provides more detailed anatomic information about the cyst than conventional US allows the sampling of both cyst fluid and any solid component in smaller lesions. Conclusions Despite a remarkable increase in the number of cystic lesions of the pancreas detected in clinical practice, the number of cystic neoplasms misdiagnosed as pseudocysts has decreased. The likely explanation is the increasing use of various imaging modalities and image-guided aspiration and biopsy. If the patient has no history of pancreatitis and no history of pancreatic trauma or pancreatic surgery and the findings from imaging do not allow conclusive diagnosis, a follow-up imaging study or image-guided aspiration/biopsy should be recommended.