Interactive Transcript
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So, another entity we should be
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aware of is autoimmune pancreatitis.
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As the name suggests, the underlying pathology
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is autoimmune process going on in the body.
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So our body is working against our
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own body, and antibodies are formed,
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and that can lead to some pseudomasses
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which can mimic pancreatic head masses.
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Or it can be sometime in the body or tail as well.
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So autoimmune pancreatitis is broadly
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divided into type 1 and type 2.
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With the type 1, the IgG4 levels are seen in the
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serum as well as the tissue if you biopsy it.
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But in type 2, the IgG4 is not found.
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That is the problem.
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So if you do a blood test, it will be negative.
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So in IgG1, the pancreas can be diffusely
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involved, or it can be just a focal disease.
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And that is the presentation which
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is going to mimic with the cancer.
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So diffused disease can be seen in 60 percent of
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the patient with type 1, and focal disease can be
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seen with 40 percent of the patient with type 1.
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But that number can go high,
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presenting with focal disease.
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In type 2, where the serum markers were
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negative, and we have no clue otherwise,
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whether it is autoimmune pancreatitis or
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not, in up to 85 percent of the patients.
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And that, that is what mimics with the mass.
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It can look like mass.
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Okay?
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And the point here is, the extra pancreatic
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tissue involvement, like involving CVD,
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or intra hepatic bile ducts, that can be seen
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with type 1, but it is not present in type 2.
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So we have no other clue.
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Okay?
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Only organ which can be involved with
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type 2 is colon, ulcerative colitis,
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can be present in 30 percent of the patient.
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Ulcerative colitis can also be present here,
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but not the way it is present in type 2.
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But there could be other involvement of the
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bile duct or some other tissues as well.
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So the point here is, the type 2 is the one
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which is going to be more controversial.
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And here we play the classical role
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because we diagnose that on MRs.
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This can be diagnosed with IgG4,
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but there is IgG4 is negative in this case.
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So we are going to play a crucial role here
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because we are the first person who is going to
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call it a mass versus autoimmune pancreatitis
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and we can prove it just by imaging, just by
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following it up after the steroid is given.
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The good news is if you give a steroid and
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follow these patients, type 2 will never
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recur back, but type 1 will recur back.
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So recurrence is common. The steroid is given
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to type 1, but they will never recur back.
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So if we diagnose on MR, and if they're treated
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with the steroid, it will never come back.
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So we have a crucial role in diagnosing
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autoimmune pancreatitis, and diagnosing it,
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or differentiating it with the adenocarcinoma,
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and we can play a very, very crucial role here.
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