In addition to clinical manifestations, the following examination methods can be selected for the diagnosis of elderly pancreatic cancer.
One, Tumor Marker Detection
1. Carcinoembryonic antigen (CEA)
CEA is a tumor-associated antigen extracted from colon adenocarcinoma and is a tumor embryonic antigen, which is a glycoprotein. It can increase in digestive tract tumors such as colon cancer, pancreatic cancer, gastric cancer, lung cancer, etc. The sensitivity and specificity of CEA for diagnosing pancreatic cancer are both low, with only 30% of advanced pancreatic cancer patients showing elevated serum CEA. Some reports indicate that the sensitivity and specificity of CEA are 35% to 51% and 50% to 80% respectively. Due to the possibility of false positives in both normal people and patients with chronic pancreatitis, the elevation of serum CEA level has only a reference value for the diagnosis of pancreatic cancer. It is reported that measuring CEA in pancreatic juice, combined with cytological examination of pancreatic juice, can increase the sensitivity of diagnosis to 86%. CEA cannot be used as a screening test for asymptomatic populations, nor can it be used as a method for early diagnosis of pancreatic cancer.
2. Carbohydrate antigen determinant CA19-9
It is a glycoprotein extracted from colon cancer cell lines and has high sensitivity and relative specificity for pancreatic cancer. The normal serum CA19-9 value in humans is 8.4 ± 4 U/ml, and 37 U/ml is the critical value. The diagnostic sensitivity for pancreatic cancer reaches 79%, while it is only 18% for colon cancer, and none of the patients with pancreatitis show an increase. It helps in differentiation. Recently, the application of immunoperoxidase staining method for detecting CA19-9 has been introduced, which can reach an accuracy of 86% for diagnosing pancreatic cancer. The content of CA19-9 is positively correlated with the size of the tumor, and those with low levels have a higher possibility of surgical resection. After tumor resection, CA19-9 levels significantly decrease to normal, indicating a better prognosis.
3. Pancreatic cancer embryonic antigen (POA)
POA is an antigen found in normal fetal pancreatic tissue and pancreatic cancer cells. The normal value is 4.0 ± 1.4 U/ml, and a value above 7.0 U/ml is considered positive. Literature reports that the incidence of elevated POA in patients with pancreatic cancer is 73%, while the positive rates in gastric cancer and colon cancer are 49% and 33% respectively. The sensitivity and specificity of POA for diagnosing pancreatic cancer are 73% and 68% respectively, but about 10% of cases of pancreatitis can show false positives. It has certain reference value for the diagnosis of pancreatic cancer, but the specificity is not high, so its wide application is still limited.
4. Pancreatic cancer-related antigen (PEAA) and pancreatic-specific antigen (PSA)
PEAA is a glycoprotein isolated from the ascites of pancreatic cancer patients. The normal upper limit of PEAA in serum is 16.2 ng/L, and 53% of patients with pancreatic cancer have positive PCAA. Among stage I patients, the positive rate is 50%, but the positive rates in patients with chronic pancreatitis and cholelithiasis are also as high as 50% and 38% respectively, indicating that the specificity of PCAA for diagnosing pancreatic cancer is poor. PSA is a single-chain protein extracted from normal human pancreas and is an acidic glycoprotein. The normal level in humans is 8.2 μg/L, and a level above 21.5 μg/L is considered positive. 66% of patients with pancreatic cancer have positive serum PSA, among whom 60% of stage I patients are positive. The positive rates in patients with benign pancreatic diseases and cholelithiasis are 25% and 38% respectively. The sensitivity and specificity of PSA and PCAA combined detection for pancreatic cancer are significantly higher than those of single detection, reaching 90% and 85% respectively.
The levels of carbohydrate antigen-199 (CA-199), pancreatic embryonic antigen (PEA), and tumor-specific growth factor (TSGF) were detected by ELISA, and the colorimetric method was used to detect TSGF. The contents were all significantly increased, with positive rates of 85.4%, 87.5%, and 83.3%, respectively. The combined detection of the three has a positive rate of 100% for the diagnosis of pancreatic cancer. The dynamic detection of CA-199, PEA, and TSGF is an important indicator for the diagnosis of pancreatic cancer, the observation of the efficacy of pancreatic cancer, and the judgment of prognosis.
2. Other laboratory tests
1. CCK-PZ and secretin test
After intravenous infusion of CCK-PZ and secretin, pancreatic juice is collected from the duodenum. The normal value is that the flow rate after the injection of secretin is >90ml at 80min, the highest concentration of bicarbonate is >80mmol/L, and the total excretion of amylase after the injection of CCK-PZ is >7500 SomogyiU/80min. Pancreatic cancer patients mainly have significantly reduced enzyme values and bicarbonate concentrations.
2. BT-PABA test
The oral synthetic polypeptide BT-PABA test is used to determine the secretion function of trypsinogen, with a normal value of 63.52±10.53%. If it is below 30%, it is definitely indicative of low pancreatic secretion function, which is seen in pancreatic cancer and chronic pancreatitis.
3. Serum ribonuclease
Some reports show that 90% of pancreatic cancer patients have elevated serum ribonuclease levels, >250U/ml (normal value
4. Lactoferrin
LF is a glycoprotein combined with iron, which can be detected in various exocrine fluids such as milk, pancreatic juice, saliva, bile, bronchial secretions, and special granules of neutrophils. Detection of LF in pancreatic juice helps to differentiate pancreatic cancer from chronic pancreatitis.
In recent years, due to the rapid development of imaging examination technology and the progress of experimental diagnostic methods, the diagnostic level of pancreatic cancer has been improved, but the detection rate of early pancreatic cancer (tumor diameter ≤ 2cm, capsule not invaded, no metastasis) is still very low, and it is necessary to continue to explore.
3. X-ray examination
Low-tension duodenal angiography is significant for the diagnosis of pancreatic cancer, as pancreatic cancer can affect adjacent hollow organs, causing them to shift or be invaded, the most common being the
2. Retrograde pancreatic and bile duct造影 (ERCP)
By inserting a catheter into the ampulla opening through the duodenoscope to perform ERCP, the diagnostic rate for pancreatic cancer is about 85% to 90%, which is higher than that of B-ultrasonography or CT. It can detect pancreatic cancer earlier, especially for those with lower bile duct and pancreatic duct obstruction, which has significant clinical significance. The ERCP manifestations can be divided into obstruction type, local stenosis type, progressive stenosis type, and abnormal branch type, etc. The main pancreatic duct and common bile duct show double duct sign, etc. The advantages are that it can observe whether the pancreatic head lesion infiltrates the duodenal papilla and the morphological changes of the pancreatic duct and bile duct. It is the most valuable method to show the pancreatic duct.
3. Selective celiac artery angiography
By inserting a catheter into the celiac artery, superior mesenteric artery, and its branches through the abdominal aorta, selective angiography is performed. The accuracy rate of selective angiography is about 90%. In pancreatic cancer, the main manifestations are variations in the morphology of intra-abdominal or peripancreatic arteries and veins, including serrated changes in the vascular wall, narrowing, angular changes, namely displacement, interruption, and obstruction, etc.
4. Percutaneous liver puncture cholangiography (PTC)
It can show the location, degree of bile duct obstruction, and differentiate it from stones. For example, if there is dilation of the intrahepatic bile ducts, the success rate of puncture under the guidance of B-ultrasonography is over 90%.
IV. CT examination and MRI imaging
1. CT examination
It is a non-invasive imaging technique that can observe the position, contour, and tumor manifestations of the pancreas more clearly. CT has a diagnostic rate for pancreatic cancer of about 75% to 88%. The main manifestations of pancreatic cancer include local mass, partial or abnormal enlargement of the pancreatic shape, disappearance of the fat layer around the pancreas, tumor, and edema of the body and tail adjacent to the pancreatic head. Due to necrosis of the tumor or obstruction of the pancreatic duct, secondary cystic dilation occurs, presenting as focal areas of reduced density.
2. MRI imaging
The MRI of pancreatic cancer shows irregular T1 values, with higher T1 values at the center of the tumor. If there is bile duct obstruction at the same time, it is considered a specific manifestation of pancreatic cancer, which is significant for distinguishing between benign and malignant tumors.
3. MRCP
It has characteristics such as non-invasiveness, no trauma, no serious complications, short examination time, no need for contrast agent injection, no X-ray damage, and can clearly show the condition of bile ducts and pancreatic ducts. Its diagnostic rate for pancreatic cancer is similar to that of ERCP.
V. Ultrasonography
1. B-ultrasonography
It can be understood whether there is dilation of the extrahepatic bile ducts, whether there are tumors at the lower end of the pancreatic head or common bile duct, the location of extrahepatic bile duct obstruction, the nature, and the degree of bile duct dilation. The ultrasound image of pancreatic cancer shows localized enlargement or lobular changes of the pancreas; the edges are unclear, and the echo is reduced or disappeared.
2. Endoscopic ultrasound examination
For the diagnosis of pancreatic cancer, including early-stage pancreatic cancer, it has great value and can make a certain diagnosis on the possibility of surgical resection. The endoscopic ultrasound examination of pancreatic cancer is manifested as:
(1) Hyperechoic solid mass, internally visible irregular spots, presenting as circular or nodular, with rough edges of the mass. The typical lesion has a flame-like outer contour.
(2) The infiltration of pancreatic cancer into surrounding large blood vessels is manifested as rough edges of blood vessels and compression by the tumor, and so on.
Sixth, laparoscopic examination
Under laparoscopic direct vision, the normal surface of the pancreas is yellowish-white. Due to the special anatomical position of pancreatic head cancer, laparoscopic examination can only be diagnosed based on indirect signs, which are manifested as significant gallbladder enlargement, green liver, large gastric窦side irregular mass-like protuberance and deformation, varices of the right gastroepiploic artery and superior pancreaticoduodenal artery, and changes such as liver and peritoneal metastasis. The direct signs of pancreatic body and tail cancer are pancreatic masses with irregularly proliferating small blood vessels accompanied by vascular interruption, narrowing, and hard texture. The indirect signs include varices of the coronary vein of the stomach and the great omentum vein of the stomach, disordered omental blood vessels, green liver, and enlarged gallbladder, and so on.
Seventh, pancreatic biopsy and cytological examination
Fine needle aspiration biopsy (FNA) before or during surgery is used for diagnosing pancreatic cancer and obtaining pancreatic cells. The methods include:
1. Direct puncture of the pancreas from the pancreatic duct and duodenal wall through the duodenoscope;
2. Under the guidance of ultrasound, CT, or angiography, percutaneous fine needle puncture of pancreatic tissue is performed;
3. Under direct vision during surgery, Kim performed FNA on 30 patients with pancreatic lesions, with an accuracy rate of 80%, specificity of 100%, sensitivity of 79%, positive predictive value of 100%, which is one of the very effective methods for diagnosing pancreatic cancer.