Type 3c diabetes

Medical condition From Wikipedia, the free encyclopedia

Type 3c diabetes (also known as pancreatogenic diabetes) is diabetes that comes secondary to pancreatic diseases,[1] involving the endocrine and exocrine (digestive) functions of the pancreas. It also occurs following surgical removal of the pancreas.

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Type 3c diabetes
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Around 5–10% of cases of diabetes in the Western world are related to pancreatic diseases. Chronic pancreatitis is most often the cause.[1][2]

Presentation

The symptoms of Type 3c diabetes are the same as other forms of diabetes. They include:[citation needed]

  • Increased thirst (polydipsia) and dry mouth.
  • Frequent urination.
  • Fatigue.
  • Blurred vision.
  • Unexplained weight loss.
  • Numbness or tingling in hands or feet.
  • Slow-healing sores or cuts.
  • Frequent skin and/or vaginal yeast infections.

People with Type 3c diabetes typically also have symptoms of exocrine pancreatic insufficiency, which include:[citation needed]

  • Abdominal pain, gas and bloating.
  • Constipation.
  • Diarrhoea.
  • Fatty stools (pale, oily, foul-smelling faeces that float).
  • Unexplained weight loss.

The same complications that occur for other types of diabetics (type 1 and type 2) may occur for type 3c diabetics. These include retinopathy, nephropathy, neuropathy, and cardiovascular disease. Patients with this condition are advised to follow the same risk-reduction guidelines as the other diabetics do and keep blood sugars as normal as possible to minimize any complications.[citation needed]

Cause

There are multiple causes. Some of which identified are:

Diagnosis

More information Diagnostic Criteria for T3cDM ...
Diagnostic Criteria for T3cDM
Major criteria (all must be fulfilled):
  • Presence of exocrine pancreatic insufficiency (according to monoclonal fecal elastase-1 or direct function tests).
  • Pathological pancreatic imaging: (by endoscopic ultrasound, MRI, or CT)
  • Absence of T1DM-associated autoimmune markers (autoantibodies).
Minor Criteria:
  • Impaired β-cell function
  • No excessive insulin resistance (e.g. as measured by HOMA-IR).
  • Impaired incretin (e.g. GIP) or pancreatic polypeptide secretion.
  • Low serum levels of lipid (fat) soluble vitamins (A, D, E, or K).
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Management

The condition can be managed by many factors.[citation needed]

Medications

Medications such as insulin may be given in order to lower blood sugars. For not so high blood sugars, oral treatments in the form of a pill or capsule may be given.

Usually, insulin requirements are lower than in type 1 diabetes (SAID).[5] However, therapeutic challenges may arise from the fact that hypoglycaemia is a common complication, owing to the lack of alpha cells.[5]

See also

References

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