Multiple endocrine neoplasia type 1 screening

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Multiple endocrine neoplasia type 1 Microchapters

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Overview

Historical Perspective

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Pathophysiology

Causes

Differentiating Multiple endocrine neoplasia type 1 from other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications and Prognosis

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Template:CMGG; Associate Editor(s)-in-Chief: Ammu Susheela, M.D. [1]

Overview

Screening

Screening and surveillance for MEN1 may employ a combination of biochemical tests and imaging. Available recommendations are summarized in the following table.

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Biochemical Test or Procedure Condition Screened For Age Screening Initiated (y) Frequency
Serum prolactin and/or insulin-like growth factor 1 Pituitary tumors 5 Every 1 y
Fasting total serum calcium and/or ionized calcium and PTH Parathyroid tumors and PHPT 8 Every 1 y
Fasting serum gastrin Duodenopancreatic gastrinoma 20 Every 1 y
Chromogranin A, pancreatic polypeptide, glucagon, and vasointestinal polypeptide Pancreatic NETs <10years Every 1 y
Fasting glucose and insulin Insulinoma 5 Every 1 y
Brain MRI Pituitary tumors 5 Every 3–5 y based on biochemical results
Abdominal CT or MRI Pancreatic NETs 20 Every 3–5 y based on biochemical results
Abdominal CT, MRI, or endoscopic US Pancreatic NETs <10 Every 1 y