Skip to main content

Acromegaly

Julie A Creech, DO, CAQSM and Nicholas Wayne Ginther, MD Reviewed 04/2024
 


BASICS

DESCRIPTION

  • Acromegaly: a rare endocrinologic disease characterized by excess secretion of growth hormone (GH), resulting in a syndrome of coarsened facial features and overgrowth of the jaw, ha...

DIAGNOSIS

HISTORY

  • Musculoskeletal

    • Enlarging shoe and ring size

    • Arthralgias/myalgias

  • Neurologic

    • Headache

    • Vision changes, particularly temporal hemianopsia

    • Hand numbness/carpal tunnel syndrome

    • Fatigue, weakness

    • ...

TREATMENT

  • Goals of treatment:

    • Decrease the serum IGF-1 level to within the reference range for the patient's age and sex.

    • Lower serum GH to <1 mcg/L

    • Ameliorate symptoms without causing other pituitary...

ONGOING CARE

Following successful resection with normalization of IGF-1 levels, patients should continue to be monitored for recurrence. Regular appointments with endocrinology and neurosurgical speci...

REFERENCES

1
Fleseriu M, Biller BMK, Freda PU, et al. A Pituitary Society update to acromegaly management guidelines. Pituitary. 2021;24(1):1-13. doi:10.1007/s11102-020-01091-7
2
Ogedegbe OJ, Yar Cheema ...

SEE ALSO

Algorithm: Tall Stature 

CODES

ICD10

E22.0 Acromegaly and pituitary gigantism 

SNOMED

  • 74107003 Acromegaly (disorder)

  • 240089002 Myopathy in acromegaly (disorder)

  • 230581008 Neuropathy in acromegaly (disorder)

  • 80849007 Gigantism (diso...

CLINICAL PEARLS

  • The onset of acromegaly is insidious and may be initially subtle.

  • The serum IGF-1 level is the preferred screening test and is elevated in acromegaly. An elevated IGF-1 should prompt an...

Subscribe to Access Full Content

Sign Up for a 10-Day Free Trial

Sign up for a 10-day FREE Trial now and receive full access to all content.

 
×