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(Q45.2) Congenital pancreatic cyst
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21 601 in individuals diagnosis congenital pancreatic cyst confirmed
1 940 deaths with diagnosis congenital pancreatic cyst
9% mortality rate associated with the disease congenital pancreatic cyst
Diagnosis congenital pancreatic cyst is diagnosed Men are 0.76% more likely than Women
10 883
Men receive the diagnosis congenital pancreatic cyst
975 (9.0 %)Died from this diagnosis.
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10 718
Women receive the diagnosis congenital pancreatic cyst
965 (9.0 %)Died from this diagnosis.
Risk Group for the Disease congenital pancreatic cyst - Men and Women aged 0
In Men diagnosis is most often set at age 0-19, 25-59, 65-84
Less common in men the disease occurs at Age 20-24, 60-64, 85-95+Less common in women the disease occurs at Age 45-49, 55-59, 85-95+
In Women diagnosis is most often set at age 0-44, 50-54, 60-84
Disease Features congenital pancreatic cyst
Absence or low individual and public risk
Congenital pancreatic cyst - what does this mean
Congenital pancreatic cysts are rare, non-hereditary cysts that form in the pancreas during fetal development. they are usually asymptomatic and are usually found incidentally during imaging studies such as ultrasound or ct scans. they may be filled with fluid, or they may contain solid material. treatment is usually not required, but in some cases they may need to be surgically removed.
What happens during the disease - congenital pancreatic cyst
Congenital pancreatic cysts are usually caused by an abnormal development of the pancreas during fetal development. this can lead to the formation of cysts in the pancreas which can be filled with fluid or other material. these cysts can cause a wide range of symptoms depending on their size and location, including abdominal pain, nausea, and vomiting.
Clinical Pattern
More details coming soon
How does a doctor diagnose
- Physical examination
- Blood tests
- Imaging tests such as ultrasound, CT scan, MRI
- Endoscopic retrograde cholangiopancreatography (ERCP)
- Endoscopic ultrasound (EUS)
- Percutaneous transhepatic cholangiography (PTC)
- Cyst aspiration and biopsy
Treatment and Medical Assistance
Main goal of the treatment: To reduce the size of the cyst and reduce the risk of complications.
- Medication to reduce inflammation and pain
- Surgery to remove the cyst
- Endoscopic Ultrasound to monitor the cyst and assess the need for surgery
- Chemotherapy to shrink the cyst
- Radiation therapy to reduce the size of the cyst
- Endoscopic retrograde cholangiopancreatography (ERCP) to remove the cyst
- Intravenous fluids to reduce the risk of dehydration
- Nutritional support to maintain adequate nutrition
- Lifestyle changes to reduce the risk of complications
18 Days of Hospitalization Required
Average Time for Outpatient Care Not Established
Congenital pancreatic cyst - Prevention
The best way to prevent congenital pancreatic cysts is to ensure that pregnant women receive regular prenatal care, including ultrasounds to detect any abnormalities. it is also important to maintain a healthy lifestyle, including a balanced diet and regular exercise, to reduce the risk of developing this condition.