Acromegaly resident survival guide

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Tayyaba Ali, M.D.[2]

Overview

This section provides a short and straight to the point overview of the disease or symptom. The first sentence of the overview must contain the name of the disease.

Causes

Life Threatening Causes

Life-threatening causes include conditions that may result in death or permanent disability within 24 hours if left untreated.

Common Causes

Diagnosis

The approach to diagnosis of Acromegaly is based on a step-wise testing strategy. Below is an algorithm summarising the identification and laboratory diagnosis of Acromegaly.

 
 
 
 
 
 
 
 
 
 
 
 
Characterize the symptoms:
Headaches
❑ Enlargement of the hands (change in ring or glove size) and feet (change in shoe size)
Lethargy
Hyperhidrosis (excessive sweating)
Paraesthesia
Sexual dysfunction [1]
Fatigue
Jaw pain
❑ Body odor
Blood in the stool
Sleep apnea
Weight gain [2]
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Examine the patient:
❑ HEENT

❑ Musculoskeletal exam:

❑ Neurological exam:

  • Decreased muscle strength and power (weakness)

❑ Cardiovascular exam:

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

Treatment

Shown below is an algorithm summarizing the treatment of [[Acromegaly]] according the the [...] guidelines.

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Transphenoidal surgery
❑ Complete resection
❑ Tumors that are unresectable, a surgical debulking procedure may be performed followed by medical therapy
 
Yes
 
Patient is not a surgical candidate
❑ Patient preference
❑ High risk due to medical comorbidities
❑ Unresectable tumors
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Are the following criteria met postoperatively?
❑ Morning serum GH the day after surgery <1ng/ml
❑ 12 weeks postoperative:
  • Normal serum IGF-1 (for age and gender)
  • No evidence of residual tumor on pituitary MRI
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Yes
 
No
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Remission
❑ Monitor with annual IGF-1
 
Is there residual tumor that appears resectable and readily accessible (eg, not invading the cavernous sinus)?
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Perform MRI for clinical or biochemical evidence of recurrence
 
Medical therapy
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Failure of medical therapy
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Radiation therapy
❑ Stereotactic radiotherapy is most common method
 
 
 
 
 

Do's

  • The content in this section is in bullet points.

Don'ts

  • The content in this section is in bullet points.

References

  1. 1.0 1.1 Molitch ME (1992). "Clinical manifestations of acromegaly". Endocrinol Metab Clin North Am. 21 (3): 597–614. PMID 1521514.
  2. 2.0 2.1 2.2 "Acromegaly: MedlinePlus Medical Encyclopedia".


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