Acromegaly resident survival guide: Difference between revisions

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* No evidence of residual tumor on pituitary MRI</div>}}
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Revision as of 06:43, 20 August 2020

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[2]
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Examine the patient:
❑ HEENT

❑ Musculoskeletal exam:

  • Joint pain
  • Limited joint movement
  • Swelling of the bony areas around a joint [2]

Fever and neurological signs are seen in TTP
Hemoglobinuria in some cases
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

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
 
 
 
 
 
 
 
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
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

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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