Cushing's Syndrome: Difference between revisions

No edit summary
(Added categories)
 
(87 intermediate revisions by 11 users not shown)
Line 1: Line 1:
<div class="noeditbox">Welcome to [[Pathophysiology of Complex Patient Problems|PT 635 Pathophysiology of Complex Patient Problems]] This is a wiki created by and for the students in the School of Physical Therapy at Bellarmine University in Louisville KY. Please do not edit unless you are involved in this project, but please come back in the near future to check out new information!!</div><div class="editorbox">
<div class="editorbox">
'''Original Editors '''-&nbsp;Jessica Stevenson from [[Pathophysiology of Complex Patient Problems|Bellarmine University's&nbsp;Pathophysiology of Complex Patient Problems project.]]  
'''Original Editors ''' - [[User:Jessica Stevenson|Jessica Stevenson]] from [[Pathophysiology of Complex Patient Problems|Bellarmine University's&nbsp;Pathophysiology of Complex Patient Problems project.]]  


'''Lead Editors''' - Your name will be added here if you are a lead editor on this page.&nbsp; [[Physiopedia:Editors|Read more.]]
'''Top Contributors''' - {{Special:Contributors/{{FULLPAGENAME}}}} &nbsp;  
</div>
</div>  
== Definition/Description&nbsp;<br> ==
== Introduction ==
[[File:Cushing's syndrome diag.png|thumb|Cushing's syndrome]]
Cushing’s syndrome is a general term for increased secretion of cortisol by the [[Adrenal Glands|adrenal]] cortex.


Cushing’s syndrome is a general term for increased secretion of cortisol by the adrenal cortex. When corticosteroids are administered externally, a condition of hypercortisolism called iatrogenic Cushing’s syndrome occurs.&nbsp;&nbsp;<ref name="DD">Goodman CC, Snyder KS. Differential Diagnosis for Physical Therapists: Screening for Referral. Philadelphia : W.B. Saunders Company; 2006: 473-475</ref> When the hypercotisolism results from an oversecretion of ACTH from the pituitary, the condition is called Cushing’s disease. The clinical presentation is the same for all of these conditions. <ref name="Path">Goodman CC, Fuller KS. Pathology: Implications for the Physical Therapist 3rd ed. St. Louis: Saunders Elsevier; 2009: 481-483.</ref><br>
# When [[Corticosteroid Medication|corticosteroids]] are administered externally, a condition of hypercortisolism called iatrogenic Cushing’s syndrome occurs.
# When the hypercortisolism results from an oversecretion of Adrenocorticotropic hormone (ACTH) from the pituitary, the condition is called Cushing’s disease.  


*ACTH: Adrenocorticotropic hormone<br>
The clinical presentation is the same for all of these conditions.<ref name="DD">Goodman CC, Snyder KS. Differential Diagnosis for Physical Therapists: Screening for Referral. Philadelphia : W.B. Saunders Company; 2006: 473-475</ref> <ref name="Path">Goodman CC, Fuller KS. Pathology: Implications for the Physical Therapist 3rd ed. St. Louis: Saunders Elsevier; 2009: 481-483.</ref>
== Epidemiology ==
[[File:Kidney and adrenal gland.jpeg|right|frameless]]
The actual incidence and prevalence of Cushing syndrome are not known. The prevalence of the disease is highly variable across different ethnic and cultural groups depending upon the frequency and spectrum of the medical conditions requiring steroid-based therapy.


== Prevalence<br> ==
# Of the known cases, iatrogenic hypercortisolism outweighs the endogenous causes,
# Of the endogenous causes, pituitary-mediated ACTH production accounts for up to 80% of cases of hypercortisolism, followed by adrenals, unknown source, and ectopic ACTH production secondary to malignancies<ref name=":0">Chaudhry HS, Singh G. Cushing syndrome. InStatPearls [Internet] 2021 Jul 30. StatPearls Publishing. Available:https://www.ncbi.nlm.nih.gov/books/NBK470218/ (accessed 12.5.2022)</ref>


Non-iatrogenic Cushing’s syndrome occurs mainly in women, with an average age of onset of 20 to 40 years, although it can be seen in people up to age 60 years. <ref name="Path" />
== Etiology ==
[[File:Corticosteroid.jpg|thumb|522x522px|Corticosteroid Medications]]
There are two main etiologies of Cushing syndrome:
 
# Endogenous hypercortisolism: results from excessive production of cortisol by adrenal glands and can be ACTH-dependent and ACTH-independent. ACTH-secreting pituitary adenomas (Cushing disease) and ectopic ACTH secretion by neoplasms are responsible for ACTH-dependent Cushing. Adrenal hyperplasia, adenoma, and carcinoma are major causes of ACTH-independent Cushing syndrome.
# Exogenous hypercortisolism: the most common cause of Cushing syndrome, mostly iatrogenic and results from the prolonged use of [[Corticosteroid Medication|glucocorticoids]]<ref name=":0" />.


== Characteristics/Clinical Presentation  ==
== Characteristics/Clinical Presentation  ==
[[File:Cushings-syndrome2.jpg|alt=|right]]


Clinical manifestations include “moon” face (very round), buffalo hump (truncal obesity with prominent supraclavicular and dorsal cervical fat pads) <ref name="Merck">Beers MH, Porter RS, Jones TV, Kaplan JL, Berkwits M. The Merck Manual of Diagnosis and Therapy 18th ed. Whitehouse Station:Merck Research Laboratories; 2006: 1212-1214.</ref>, protuberant abdomen with accumulation of fatty tissue and stretch marks with purple striae, muscle wasting and weakness, thin extremities, decreased bone density (especially spine), kyphosis and back pain (secondary to bone loss), easy bruising and poor wound healing due to thin and atrophic skin <ref name="Merck" />, acne, psychiatric or emotional disturbances, impaired reproductive function (decreased libido and changes in menstrual cycle, and diabetes mellatis. In women, masculinizing effects such as hypertrichosis, breast atrophy, voice changes, and other signs of virilism are noted. Cessation of linear growth is characteristic in children.&nbsp;<ref name="DD" /> <ref name="Merck" />
Clinical manifestations include:
 
== Associated Co-morbidities  ==
 
Cushing’s syndrome involves the HPA axis causing excess cortisol release from the adrenal glands. When the normal function of the glucocorticoids becomes exaggerated, a wide range of physiologic responses can be triggered. <ref name="Path" />
 
Co-morbidities involved with Cushing’s disease are persistent hyperglycemia, cardiac hypertrophy and hypertension, proximal muscle wasting (protein tissue wasting), osteopenia or osteoporosis, hypokalemia, mental changes and memory loss, depression, renal calculi, increased susceptibility to infection, adrenal hyperplasia and adrenal tumors&nbsp;<ref name="Path" /> <ref name="Merck" />&nbsp;<ref name="DD" /><br><br>
 
== Medications  ==
 
Initially, the patient’s general condition should be supported by high protein intake and appropriate administration of vitamin K. If clinical manifestations are severe, it may be reasonable to block corticosteroid secretion with metyrapone 250 mg to 1 g pot id or ketoconazole 400 mg po once/day, increasing to a maximum of 400 tid. Ketoconazole is more readily available but slower in onset and sometimes hepatatoxic. <ref name="Merck" />
 
Adrenal inhibitors, such as metyrapone 500 mg pot id (and up to a total of 6 g/day) or mitotane 0.5 g po once/day, increasing to a maximum of 3 to 4 g/day, usually control severe metabolic disturbances (eg. Hypokalemia). When mitotane is used, large doses of hydrocortisone or dexamethasone may be needed. Measures of cortisol production may be unreliable, and severe hypercholesterolemia may develop. Ketoconazole 400 to 1200 mg po once/day also blocks corticosteroid synthesis, although it may cause liver toxicity and can cause addisonian symptoms. Alternatively, the corticosteroid receptors can be blocked with mifepristone (RU 486). Mifepristone increases plasma cortisol but blocks effects of the corticosteroid. Sometimes ACTH-secreting tumors respond to long-acting somatostatin analogs, although administration for &gt; 2 years requires close follow-up, because mild gastritis, gall stones, cholangitis, and malabsorption may develop. <ref name="Merck" /><br><br>


== Diagnostic Tests/Lab Tests/Lab Values  ==
* “moon” face (very round),
* buffalo hump (truncal obesity with prominent supraclavicular and dorsal cervical fat pads) <ref name="Merck">Beers MH, Porter RS, Jones TV, Kaplan JL, Berkwits M. The Merck Manual of Diagnosis and Therapy 18th ed. Whitehouse Station:Merck Research Laboratories; 2006: 1212-1214.</ref>,
* protuberant abdomen with accumulation of fatty tissue and stretch marks with purple striae,
* muscle wasting and weakness,
* thin extremities,
* decreased bone density (especially spine),
* [[kyphosis]] and back pain (secondary to bone loss),
* easy bruising and poor wound healing due to thin and atrophic skin <ref name="Merck" />,
* acne,
* psychiatric or emotional disturbances,
* impaired reproductive function (decreased libido and changes in menstrual cycle, and
* diabetes mellitus.


add text here <br>
In women, masculinizing effects such as hypertrichosis, breast atrophy, voice changes, and other signs of virilism are noted. Cessation of linear growth is characteristic in children.&nbsp;<ref name="DD" /> <ref name="Merck" />
== Complications ==


== Causes  ==
Complications include:


add text here <br>
* Excess hair growth
* [[Osteoporosis]]
* Susceptibility to infections
* [[Diabetes Mellitus Type 2|Type 2 diabetes]]
* Peptic ulcer disease
* [[Hypertension]]<ref name=":0" />


== Systemic Involvement  ==
== Diagnosis ==
Taking glucocorticoid medications is the most common cause of Cushing syndrome. If this is the case other tests are not needed. Cushing syndrome from endogenous cortisol production can be difficult to diagnose because other conditions have similar signs and symptoms. Diagnosing Cushing syndrome can be a long and extensive process. The below tests can help find the cause:


add text here
* [[Urine]] and [[Blood Tests|blood tests]]: measure [[Hormones|hormone]] levels and show whether person is producing excessive cortisol. The doctor might also recommend other specialized tests that involve measuring cortisol levels before and after using hormone medications to stimulate or suppress cortisol.
* Saliva test. Cortisol levels normally rise and fall throughout the day. In people without Cushing syndrome, levels of cortisol drop significantly in the evening. By analyzing cortisol levels from a small sample of saliva collected late at night, doctors can see if cortisol levels are too high.
* Imaging tests. CT or MRI scans can provide images of the pituitary and adrenal glands to detect abnormalities, eg tumors.
* Petrosal sinus sampling. This test can help determine whether the cause of Cushing syndrome is rooted in the pituitary or somewhere else. For the test, blood samples are taken from the veins that drain the pituitary gland (petrosal sinuses).


== Medical Management (current best evidence)  ==
== Management ==
Treatments for Cushing syndrome are designed to lower the high level of cortisol in the body. The best treatment for you depends on the cause of the syndrome. Options include:


add text here
* The best therapy for iatrogenic Cushing syndrome is to taper exogenous steroids'''.''' Chronic exposure to steroids potentially suppresses the function of the adrenal and it can take several months for normal adrenal functioning to recover.  Steroids should be slowly tapered allowing adrenal functioning to recover.
* Hypercortisolism due to Cushing disease or adrenal tumor or ectopic tumor is treated with surgical resection. After the operation,  cortisol replacement medications are needed to provide the body with the correct amount of cortisol. In most cases eventually normal adrenal hormone production returns. If the surgeon can not totally remove a pituitary tumor, [[Radiation Side Effects and Syndromes|radiation]] therapy as well as surgery will be needed. Additionally, radiation may be used for people who aren't suitable candidates for surgery<ref name=":0" />.<ref>Mayo clinic Cushing Syndrome Available:https://www.mayoclinic.org/diseases-conditions/cushing-syndrome/diagnosis-treatment/drc-20351314 (accessed 13.5.2022)</ref>
* Medications can be used to control cortisol production when surgery and radiation don't work. Medical therapy may not completely improve all of the symptoms of excess cortisol. Medications to control excessive production of cortisol at the adrenal gland include ketoconazole, mitotane (Lysodren) and metyrapone (Metopirone).


== Physical Therapy Management (current best evidence)  ==
In the management of Cushing syndrome, it is crucial to treat comorbidities such as [[Diabetes Mellitus Type 1|diabetes mellitus]], [[hypertension]], [[osteoporosis]], psychiatric issues, and electrolyte disorders.<ref name=":0" />
== Physical Therapy Management ==


add text here
Therapists are more likely to treat people who have developed medication-induced Cushing’s syndrome. Exogenous [[Corticosteroid Medication|steroids]] are administered for a number of inflammatory and other disorders eg [[asthma]] or [[Rheumatoid Arthritis|rheumatoid arthritis]]. <ref name="DD" />


== Alternative/Holistic Management (current best evidence)  ==
Educate Clients with regard to:


add text here
* Getting  regular [[Therapeutic Exercise|exercise]] to help maintain muscles and bone mass and prevent weight gain. To maintain muscle and bone mass, weight-bearing exercises eg [[Pushups|push-ups]], [[Curl-ups|sit-ups]], or lifting weights are helpful. To prevent weight gain, [[Aerobic Exercise|aerobic]] exercise are good. eg fast [[Walking - Muscles Used|walking]], jogging, cycling, and [[Swimming: Freestyle|swimming]]. <ref name="yahoo">Caroline Rea. Cushing's Syndrome. YahooHealth. last updated 4/29/2008. http://health.yahoo.com/hormone-living/cushing-s-syndrome-home-treatment/healthwise--hw71687.html</ref>
* Education on avoiding [[falls]] and removing loose rugs and other hazards in the home. Falling may lead to broken bones and other injuries. <ref name="yahoo" />
* Pay close attention to all [[Wound Debridement|wounds]]. Too much cortisol slows wound healing. Education on proper wound healing and cleansing is important.&nbsp; Clean all wounds immediately with antibacterial soap and use antibiotic ointment and dressings to prevent infection. <ref name="yahoo" />


== Differential Diagnosis  ==
add text here
== Case Reports  ==
add links to case studies here (case studies should be added on new pages using the [[Template:Case Study|case study template]])<br>
== Resources <br> ==
add appropriate resources here
== Recent Related Research (from [http://www.ncbi.nlm.nih.gov/pubmed/ Pubmed])  ==
see tutorial on [[Adding PubMed Feed|Adding PubMed Feed]]
<div class="researchbox">
<rss>Feed goes here!!|charset=UTF-8|short|max=10</rss>
</div>
== References  ==
== References  ==


see [[Adding References|adding references tutorial]].
<references />  
 
<references />


[[Category:Bellarmine_Student_Project]]
[[Category:Bellarmine_Student_Project]]
[[Category:Conditions]]
[[Category:Metabolic/Endocrine]]

Latest revision as of 16:25, 7 February 2023

Introduction[edit | edit source]

Cushing's syndrome

Cushing’s syndrome is a general term for increased secretion of cortisol by the adrenal cortex.

  1. When corticosteroids are administered externally, a condition of hypercortisolism called iatrogenic Cushing’s syndrome occurs.
  2. When the hypercortisolism results from an oversecretion of Adrenocorticotropic hormone (ACTH) from the pituitary, the condition is called Cushing’s disease.

The clinical presentation is the same for all of these conditions.[1] [2]

Epidemiology[edit | edit source]

Kidney and adrenal gland.jpeg

The actual incidence and prevalence of Cushing syndrome are not known. The prevalence of the disease is highly variable across different ethnic and cultural groups depending upon the frequency and spectrum of the medical conditions requiring steroid-based therapy.

  1. Of the known cases, iatrogenic hypercortisolism outweighs the endogenous causes,
  2. Of the endogenous causes, pituitary-mediated ACTH production accounts for up to 80% of cases of hypercortisolism, followed by adrenals, unknown source, and ectopic ACTH production secondary to malignancies[3]

Etiology[edit | edit source]

Corticosteroid Medications

There are two main etiologies of Cushing syndrome:

  1. Endogenous hypercortisolism: results from excessive production of cortisol by adrenal glands and can be ACTH-dependent and ACTH-independent. ACTH-secreting pituitary adenomas (Cushing disease) and ectopic ACTH secretion by neoplasms are responsible for ACTH-dependent Cushing. Adrenal hyperplasia, adenoma, and carcinoma are major causes of ACTH-independent Cushing syndrome.
  2. Exogenous hypercortisolism: the most common cause of Cushing syndrome, mostly iatrogenic and results from the prolonged use of glucocorticoids[3].

Characteristics/Clinical Presentation[edit | edit source]

Clinical manifestations include:

  • “moon” face (very round),
  • buffalo hump (truncal obesity with prominent supraclavicular and dorsal cervical fat pads) [4],
  • protuberant abdomen with accumulation of fatty tissue and stretch marks with purple striae,
  • muscle wasting and weakness,
  • thin extremities,
  • decreased bone density (especially spine),
  • kyphosis and back pain (secondary to bone loss),
  • easy bruising and poor wound healing due to thin and atrophic skin [4],
  • acne,
  • psychiatric or emotional disturbances,
  • impaired reproductive function (decreased libido and changes in menstrual cycle, and
  • diabetes mellitus.

In women, masculinizing effects such as hypertrichosis, breast atrophy, voice changes, and other signs of virilism are noted. Cessation of linear growth is characteristic in children. [1] [4]

Complications[edit | edit source]

Complications include:

Diagnosis[edit | edit source]

Taking glucocorticoid medications is the most common cause of Cushing syndrome. If this is the case other tests are not needed. Cushing syndrome from endogenous cortisol production can be difficult to diagnose because other conditions have similar signs and symptoms. Diagnosing Cushing syndrome can be a long and extensive process. The below tests can help find the cause:

  • Urine and blood tests: measure hormone levels and show whether person is producing excessive cortisol. The doctor might also recommend other specialized tests that involve measuring cortisol levels before and after using hormone medications to stimulate or suppress cortisol.
  • Saliva test. Cortisol levels normally rise and fall throughout the day. In people without Cushing syndrome, levels of cortisol drop significantly in the evening. By analyzing cortisol levels from a small sample of saliva collected late at night, doctors can see if cortisol levels are too high.
  • Imaging tests. CT or MRI scans can provide images of the pituitary and adrenal glands to detect abnormalities, eg tumors.
  • Petrosal sinus sampling. This test can help determine whether the cause of Cushing syndrome is rooted in the pituitary or somewhere else. For the test, blood samples are taken from the veins that drain the pituitary gland (petrosal sinuses).

Management[edit | edit source]

Treatments for Cushing syndrome are designed to lower the high level of cortisol in the body. The best treatment for you depends on the cause of the syndrome. Options include:

  • The best therapy for iatrogenic Cushing syndrome is to taper exogenous steroids. Chronic exposure to steroids potentially suppresses the function of the adrenal and it can take several months for normal adrenal functioning to recover.  Steroids should be slowly tapered allowing adrenal functioning to recover.
  • Hypercortisolism due to Cushing disease or adrenal tumor or ectopic tumor is treated with surgical resection. After the operation, cortisol replacement medications are needed to provide the body with the correct amount of cortisol. In most cases eventually normal adrenal hormone production returns. If the surgeon can not totally remove a pituitary tumor, radiation therapy as well as surgery will be needed. Additionally, radiation may be used for people who aren't suitable candidates for surgery[3].[5]
  • Medications can be used to control cortisol production when surgery and radiation don't work. Medical therapy may not completely improve all of the symptoms of excess cortisol. Medications to control excessive production of cortisol at the adrenal gland include ketoconazole, mitotane (Lysodren) and metyrapone (Metopirone).

In the management of Cushing syndrome, it is crucial to treat comorbidities such as diabetes mellitus, hypertension, osteoporosis, psychiatric issues, and electrolyte disorders.[3]

Physical Therapy Management[edit | edit source]

Therapists are more likely to treat people who have developed medication-induced Cushing’s syndrome. Exogenous steroids are administered for a number of inflammatory and other disorders eg asthma or rheumatoid arthritis. [1]

Educate Clients with regard to:

  • Getting regular exercise to help maintain muscles and bone mass and prevent weight gain. To maintain muscle and bone mass, weight-bearing exercises eg push-ups, sit-ups, or lifting weights are helpful. To prevent weight gain, aerobic exercise are good. eg fast walking, jogging, cycling, and swimming. [6]
  • Education on avoiding falls and removing loose rugs and other hazards in the home. Falling may lead to broken bones and other injuries. [6]
  • Pay close attention to all wounds. Too much cortisol slows wound healing. Education on proper wound healing and cleansing is important.  Clean all wounds immediately with antibacterial soap and use antibiotic ointment and dressings to prevent infection. [6]

References[edit | edit source]

  1. 1.0 1.1 1.2 Goodman CC, Snyder KS. Differential Diagnosis for Physical Therapists: Screening for Referral. Philadelphia : W.B. Saunders Company; 2006: 473-475
  2. Goodman CC, Fuller KS. Pathology: Implications for the Physical Therapist 3rd ed. St. Louis: Saunders Elsevier; 2009: 481-483.
  3. 3.0 3.1 3.2 3.3 3.4 Chaudhry HS, Singh G. Cushing syndrome. InStatPearls [Internet] 2021 Jul 30. StatPearls Publishing. Available:https://www.ncbi.nlm.nih.gov/books/NBK470218/ (accessed 12.5.2022)
  4. 4.0 4.1 4.2 Beers MH, Porter RS, Jones TV, Kaplan JL, Berkwits M. The Merck Manual of Diagnosis and Therapy 18th ed. Whitehouse Station:Merck Research Laboratories; 2006: 1212-1214.
  5. Mayo clinic Cushing Syndrome Available:https://www.mayoclinic.org/diseases-conditions/cushing-syndrome/diagnosis-treatment/drc-20351314 (accessed 13.5.2022)
  6. 6.0 6.1 6.2 Caroline Rea. Cushing's Syndrome. YahooHealth. last updated 4/29/2008. http://health.yahoo.com/hormone-living/cushing-s-syndrome-home-treatment/healthwise--hw71687.html