Gallbladder diagnosis aims to identify gallbladder diseases such as gallstones (cholelithiasis), gallbladder inflammation (cholecystitis), or gallbladder cancer.
The following is a general outline for the diagnosis of gallbladder diseases:
The clinician will typically start with a thorough medical history. They will ask about the patient's symptoms, duration of symptoms, diet, lifestyle, and personal or family history of gallbladder disease.
The doctor will perform a physical examination that may include feeling the upper abdomen for signs of gallbladder inflammation, such as tenderness or swelling. They may also check for signs of jaundice (yellowing of the skin and the whites of the eyes).
Blood tests may be performed to detect signs of infection, liver problems, pancreatitis, or other abnormalities. Blood tests can also determine if there is an increased white blood cell count, which may suggest an infection or inflammation.
Imaging tests can help visualise gallstones, inflammation, or tumours in the gallbladder. These may include:
If gallbladder cancer is suspected, a biopsy may be performed. This involves removing a small tissue sample from the gallbladder for examination under a microscope.
Remember that not all these tests may be necessary for every patient, and the exact approach will depend on the patient's symptoms, physical exam findings, medical history, and the results of initial tests.
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