Type 1: Absolute insulin deficiency
Type 2: Insulin resistance and inadequate secretion
Etiology/Pathogenesis
•
Unknown and multifactorial
Possible autoimmune causes
Some genetic causes
Diseases of exocrine pancreas
Clinical Issues
•
Laboratory tests
Elevated random plasma and fasting glucose, hemoglobin A1c
Macroscopic
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Decreased size and weight (type 1 > type 2)
Microscopic
•
Type 1
Variation in islet size and shape with irregularly shaped islets
Reduced or absent B cells
Variably present islet inflammation
Amyloidosis almost never seen in type 1 diabetes
•
Type 2
Islet amyloidosis
Reduction in both A and B cells
Islets reduced in number but unchanged in size
•
Both types
Interlobular and interacinar fibrosis, exocrine atrophy
Exocrine atrophy
Top Differential Diagnoses
•
Normal aging may also result in decreased size and weight of pancreas, islet amyloidosis
TERMINOLOGY
Abbreviations
Definitions
•
Heterogeneous group of metabolic diseases characterized by hyperglycemia
Result of defects in insulin secretion, insulin activity, or both
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