Acromegaly resident survival guide: Difference between revisions
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{{familytree | | | | | | | A01 |A01=<div style="float: left; text-align: center; width: 20em; padding:1em;"> '''[[Acromegaly]]''' }} | {{familytree | | | | | | | A01 |A01=<div style="float: left; text-align: center; width: 20em; padding:1em;"> '''[[Acromegaly]]''' }} | ||
{{familytree | | | | |,|-|-|^|-|-|.| | | }} | {{familytree | | | | |,|-|-|^|-|-|.| | | }} | ||
{{familytree | | | | {{familytree | | | | |!| | | | | |!| | | }} | ||
{{familytree | | | |!| | | | | | | |!| | }} | {{familytree | | | B01 |-| B03 | | B02 | | |B01=<div style="float: left; text-align: left; width: 20em; padding:1em;"> '''[[Transphenoidal surgery]]'''<br>❑ Complete resection<br>❑ Tumors that are unresectable, a surgical debulking procedure may be performed followed by medical therapy|B02=<div style="float: left; text-align: left; width: 20em; padding:1em;"> '''Patient is not a surgical candidate'''<br>❑ Patient preference<br>❑ High risk due to medical comorbidities<br>❑ Unresectable tumors|B03=<div style="float: left; text-align: center; width: 10em; padding:1em;"> '''Yes'''</div>}} | ||
{{familytree | | | C01 | | | | | | |!| | | |C01=<div style="float: left; text-align: left; width: 20em; padding:1em;"> '''Are the following criteria met postoperatively?'''<br>❑ Morning serum GH the day after surgery <1ng/ml<br>❑ 12 weeks postoperative: | {{familytree | | | |!| | | |!| | | |!| | }} | ||
{{familytree | | | C01 | | |!| | | |!| | | |C01=<div style="float: left; text-align: left; width: 20em; padding:1em;"> '''Are the following criteria met postoperatively?'''<br>❑ Morning serum GH the day after surgery <1ng/ml<br>❑ 12 weeks postoperative: | |||
* Normal serum IGF-1 (for age and gender) | * Normal serum IGF-1 (for age and gender) | ||
* No evidence of residual tumor on pituitary MRI</div>}} | * No evidence of residual tumor on pituitary MRI</div>}} | ||
{{familytree | |,|-|^|.| | | | | | |!| | | }} | {{familytree | |,|-|^|.| | |!| | | |!| | | }} | ||
{{familytree | D01 | | D02 | | | | |!| | | |D01=<div style="float: left; text-align: left; width: 20em; padding:1em;"> '''Yes'''|D02=<div style="float: left; text-align: left; width: 20em; padding:1em;"> '''No'''</div>}} | {{familytree | D01 | | D02 |!| | | |!| | | |D01=<div style="float: left; text-align: left; width: 20em; padding:1em;"> '''Yes'''|D02=<div style="float: left; text-align: left; width: 20em; padding:1em;"> '''No'''</div>}} | ||
{{familytree | |!| | | |!| | | | | |!| | | | }} | {{familytree | |!| | | |!|,|(| | | |!| | | | }} | ||
{{familytree | E01 | | E02 | | | | |!|E01=<div style="float: left; text-align: left; width: 20em; padding:1em;"> '''Remission'''<br>❑ Monitor with annual IGF-1|E02=<div style="float: left; text-align: left; width: 20em; padding:1em;"> '''Is there residual tumor that appears resectable and readily accessible (eg, not invading the cavernous sinus)?'''</div>}} | {{familytree | E01 | | E02 | | | | |!|E01=<div style="float: left; text-align: left; width: 20em; padding:1em;"> '''Remission'''<br>❑ Monitor with annual IGF-1|E02=<div style="float: left; text-align: left; width: 20em; padding:1em;"> '''Is there residual tumor that appears resectable and readily accessible (eg, not invading the cavernous sinus)?'''</div>}} | ||
{{familytree | |!| | | |!|,|-|-|-|-|(| | | | }} | {{familytree | |!| | | |!|,|-|-|-|-|(| | | | }} |
Revision as of 08:12, 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:
❑ 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 | 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:
| |||||||||||||||||||||||||||||||
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
- ↑ 1.0 1.1 Molitch ME (1992). "Clinical manifestations of acromegaly". Endocrinol Metab Clin North Am. 21 (3): 597–614. PMID 1521514.
- ↑ 2.0 2.1 2.2 "Acromegaly: MedlinePlus Medical Encyclopedia".