McCune-Albright syndrome: Difference between revisions

Jump to navigation Jump to search
No edit summary
Line 1: Line 1:
{{Infobox_Disease |
__NOTOC__
  Name          = McCune-Albright syndrome |
 
  Image          = |
  Caption        = |
  DiseasesDB    = 7880 |
  ICD10          = {{ICD10|Q|78|1|q|65}} |
  ICD9          = {{ICD9|756.54}} |
  ICDO          = |
  OMIM          = 174800 |
  MedlinePlus    = 001217 |
  eMedicineSubj  = ped |
  eMedicineTopic = 1386 |
  MeshID        = D005359 |
}}
{{SI}}
{{SI}}
{{CMG}}; {{AE}} [[User:Dushka|Dushka Riaz, MD]]
{{CMG}}; {{AE}} [[User:Dushka|Dushka Riaz, MD]]

Revision as of 13:45, 29 September 2020


WikiDoc Resources for McCune-Albright syndrome

Articles

Most recent articles on McCune-Albright syndrome

Most cited articles on McCune-Albright syndrome

Review articles on McCune-Albright syndrome

Articles on McCune-Albright syndrome in N Eng J Med, Lancet, BMJ

Media

Powerpoint slides on McCune-Albright syndrome

Images of McCune-Albright syndrome

Photos of McCune-Albright syndrome

Podcasts & MP3s on McCune-Albright syndrome

Videos on McCune-Albright syndrome

Evidence Based Medicine

Cochrane Collaboration on McCune-Albright syndrome

Bandolier on McCune-Albright syndrome

TRIP on McCune-Albright syndrome

Clinical Trials

Ongoing Trials on McCune-Albright syndrome at Clinical Trials.gov

Trial results on McCune-Albright syndrome

Clinical Trials on McCune-Albright syndrome at Google

Guidelines / Policies / Govt

US National Guidelines Clearinghouse on McCune-Albright syndrome

NICE Guidance on McCune-Albright syndrome

NHS PRODIGY Guidance

FDA on McCune-Albright syndrome

CDC on McCune-Albright syndrome

Books

Books on McCune-Albright syndrome

News

McCune-Albright syndrome in the news

Be alerted to news on McCune-Albright syndrome

News trends on McCune-Albright syndrome

Commentary

Blogs on McCune-Albright syndrome

Definitions

Definitions of McCune-Albright syndrome

Patient Resources / Community

Patient resources on McCune-Albright syndrome

Discussion groups on McCune-Albright syndrome

Patient Handouts on McCune-Albright syndrome

Directions to Hospitals Treating McCune-Albright syndrome

Risk calculators and risk factors for McCune-Albright syndrome

Healthcare Provider Resources

Symptoms of McCune-Albright syndrome

Causes & Risk Factors for McCune-Albright syndrome

Diagnostic studies for McCune-Albright syndrome

Treatment of McCune-Albright syndrome

Continuing Medical Education (CME)

CME Programs on McCune-Albright syndrome

International

McCune-Albright syndrome en Espanol

McCune-Albright syndrome en Francais

Business

McCune-Albright syndrome in the Marketplace

Patents on McCune-Albright syndrome

Experimental / Informatics

List of terms related to McCune-Albright syndrome

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Dushka Riaz, MD

Overview

McCune-Albright syndrome is a rare genetic disorder caused by an activating mutation of the GNAS gene resulting in various phenotypic presentations. McCune-Albright syndrome typically presents with the triad of fibrous dysplasia, precocious puberty and café au lait spots in both genders. Other manifestations include acromegaly, Cushing’s syndrome [1] and thyroid hyperplasia or toxic nodular goiters [2]

Historical Perspective

Classification

There is no established system for the classification of McCune-Albright syndrome.

Pathophysiology

  • The pathogenesis of McCune-Albright syndrome is characterized by increased cAMP signaling in bone, skin and endocrine tissues. In bone, osteoblasts differentiation results in fibrous dysplasia. In the skin, there is stimulation of melanin production resulting in café au lait macules with irregular borders. In endocrine tissues, increased cAMP results in increased production of hormones depending on which tissue is affected including the gonads, thyroid, parathyroid, pituitary and adrenal glands. [1]
  • The GNAS gene mutation has been associated with the development of McCune-Albright syndrome, involving the cAMP pathway-associated G-protein, Gsα. [4]

Causes

McCune-Albright syndrome is caused by a missense mutation of the GNAS gene alpha subunit which becomes constitutively activated. This increases intracellular cAMP which activates downstream hormones resulting in multiple tissue types being affected and mosaicism presented in its patients. [1]

Differentiating McCune-Albright syndrome from other Diseases

For further information about the differential diagnosis, click here

Epidemiology and Demographics

  • The prevalence of McCune-Albright syndrome is between 1:100,000 and 1:1,000,000 making it very rare.

Age

  • McCune-Albright syndrome is more commonly observed among infants and young children.

Gender

  • Girls are more commonly affected with McCune-Albright syndrome than boys [5]

Race

  • There is no racial predilection for McCune-Albright syndrome.

Risk Factors

There are no risk factors for McCune-Albright syndrome.

Natural History, Complications and Prognosis

  • Early clinical features include café-au-lait macules often at birth. [6]
  • If left untreated, patients may progress to develop decreased adult stature as a result of precocious puberty.
  • Common complications of McCune-Albright syndrome include rickets because of phosphate wasting and fractures at fibrous dysplastic sites. [1]

Diagnosis

Diagnostic Criteria

  • The diagnosis of McCune-Albright syndrome is a clinical diagnosis. [1]
  • Though there are genetic tests available for the GNAS gene mutation with new PCR techniques for those who show clinical signs of the syndrome. [7]
  • Patients who present with monostotic fibrous dysplasia are required to have evidence of the pathogenic GNAS gene by molecular testing [4]

Symptoms

  • Symptoms of McCune-Albright syndrome include the following:
    • Precocious puberty being the most common presentation [8]
      • In girls presenting with recurrent cysts and cyclic menses [9]
      • In boys presenting with acne, body odor, pubic hair and penile enlargement
      • Both genders with gonadal pathologies [7]
    • Fibrous dysplasia leading to pathologic fractures or pain [1] because of fibrous tissue replacing the normal bone
      • This can be either monostotic (involving one bone) or polyostotic (involving multiple bones) [4]
      • This presents in adolescent years affecting males more than females [10]
    • Café au lait spots with “coast of Maine” irregular borders [11] are often the first presenting sign [4] and may increase over time [12]
    • Possible hyperthyroidism, Cushing syndrome, acromegaly or prolactin secretion due to increased thyroid, cortisol, growth hormone or prolactin secretion respectively depending on which tissues are affected [1]
    • Phosphate wasting with or without hypophosphatemia mediated by Fibroblast growth factor 23 (FGF23) [4]
    • Possible hepatitis, cholestasis and cardiac arrhythmias [13]
Café au lait spot

Physical Examination

  • Patients with McCune-Albright syndrome usually present with bone pain or limping.
  • Physical examination may be remarkable for:
    • Facial asymmetry due to craniofacial fibrous dysplasia
    • Hearing impairment or visual disturbances due to craniofacial fibrous dysplasia
    • Café au lait macules
    • Goiter due to hyperthyroidism
    • Macrocephaly due to excess growth hormone
    • Vaginal bleeding in females due to ovarian cysts
    • Pubic and or axillary hair and penile enlargement in males
    • Growth acceleration in both genders
    • Cushingoid features due to hypercortisolism [6]

Laboratory Findings

  • Girls will have raised estradiol levels indicating an activated hypothalamic-pituitary axis.
  • Other laboratory findings consistent with the diagnosis of McCune-Albright syndrome are elevated growth hormone which can be deduced by an oral glucose tolerance test, serum GH and prolactin measurements.
  • Evaluation of hyperthyroidism by measuring TSH, free and bound thyroxine and T3. [1]

Electrocardiogram

There are no ECG findings associated with McCune-Albright syndrome.

X-ray

The fibrous dysplasia of bone is present at multiple sites (polyostotic) and xrays would give a ground glass appearance. [7]

Echocardiography or Ultrasound

US in boys may be helpful in the diagnosis of McCune-Albright syndrome. Findings on an US suggestive of McCune-Albright syndrome include testicular ultrasounds to detect hormonally active tumors.[1]

CT scan

CT scan may be helpful in the diagnosis of McCune-Albright syndrome. Findings on CT scan suggestive of/diagnostic of McCune-Albright syndrome include fibroblastic lesions. It is helpful to identify these early in children to prevent permanent deformities. [1]

MRI

There are no MRI findings associated with McCune-Albright syndrome.

Other Imaging Findings

There are no other imaging findings associated with McCune-Albright syndrome.

Other Diagnostic Studies

  • McCune Albright may be diagnosed using total body bone scintigraphy to identify the fibrous dysplastic lesions. This should then be followed up with radiographs and CT to clearly determine the extent of the lesions.
  • It is helpful to perform baseline ophthalmic and audiologic testing for those patients whose fibrous dysplastic lesions involve the craniofacial area [4]

Treatment

Medical Therapy

  • The treatment for McCune Albright syndrome includes:
    • Precocious puberty- treatment is aimed to prevent bone age advancement [4]
      • For girls- Letrozole (aromatase inhibitor) and or tamoxifen (estrogen receptor modulator) [7]
      • For boys- treatment options are not well established
    • Fibrous dysplasia – treatment is aimed to minimize pain and fractures:
    • Endocrinopathies
      • Thyroid disease – Methimazole is effective though surgery is preferred
      • Increased growth hormone
        • Octeotride which acts as a somatostatin analog and should be monitored for signs and symptoms of gallbladder disease
        • Pegvisomant which is a growth hormone receptor antagonist and should be monitored for hepatotoxicity
      • Hypercortisolism - metyparone is effective
      • FGF23-mediated phosphate wasting with oral phosphorus and calcitriol [4]
    • Café-au-lait macules
      • There is no effective treatment [14]

Surgery

  • Surgery should be used in extreme caution for female patients with ovarian cysts because of the high risk of recurrence and resultant decrease in ovarian reserve.
  • Patients with hyperthyroidism are preferred to have a thyroidectomy with total gland resection [4]

Prevention

  • Once diagnosed, patients with McCune-Albright syndrome are followed-up with:
    • Females – early breast cancer screening
    • Males – testicular lesions by physical examination and US [4]
    • Both genders – signs of precocious puberty, growth hormone excess or growth acceleration (IGF-1 levels), monitoring thyroid function (TSH, free T4, and T3), routine radiographs for fibrous dysplasia lesions particularly to check for scoliosis, serum phosphorous to monitor for development of hypophosphatemia [4] and annual vision and hearing testing to monitor fibrotic lesions affecting these areas. [1]
  • Parents should be counseled that McCune-Albright syndrome is not inherited [4]
  • There is an increased risk for malignancies [15]
  • Patients should also be advised to avoid contact sports and optic nerve decompressions [4]

References

  1. 1.00 1.01 1.02 1.03 1.04 1.05 1.06 1.07 1.08 1.09 1.10 "StatPearls". 2020. PMID 30725777.
  2. Mastorakos G, Mitsiades NS, Doufas AG, Koutras DA (1997). "Hyperthyroidism in McCune-Albright syndrome with a review of thyroid abnormalities sixty years after the first report". Thyroid. 7 (3): 433–9. doi:10.1089/thy.1997.7.433. PMID 9226216.
  3. Manring MM, Calhoun JH (2011). "Biographical sketch: Fuller Albright, MD 1900-1969". Clin Orthop Relat Res. 469 (8): 2092–5. doi:10.1007/s11999-011-1831-0. PMC 3126964. PMID 21384213.
  4. 4.00 4.01 4.02 4.03 4.04 4.05 4.06 4.07 4.08 4.09 4.10 4.11 4.12 4.13 Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K; et al. (1993). "GeneReviews®". PMID 25719192.
  5. Lumbroso S, Paris F, Sultan C, European Collaborative Study (2004). "Activating Gsalpha mutations: analysis of 113 patients with signs of McCune-Albright syndrome--a European Collaborative Study". J Clin Endocrinol Metab. 89 (5): 2107–13. doi:10.1210/jc.2003-031225. PMID 15126527.
  6. 6.0 6.1 Spencer T, Pan KS, Collins MT, Boyce AM (2019). "The Clinical Spectrum of McCune-Albright Syndrome and Its Management". Horm Res Paediatr. 92 (6): 347–356. doi:10.1159/000504802. PMC 7302983 Check |pmc= value (help). PMID 31865341.
  7. 7.0 7.1 7.2 7.3 7.4 Pratt VM, McLeod HL, Rubinstein WS, Scott SA, Dean LC, Kattman BL; et al. (2012). "Medical Genetics Summaries". PMID 28520344.
  8. de Sanctis C, Lala R, Matarazzo P, Balsamo A, Bergamaschi R, Cappa M; et al. (1999). "McCune-Albright syndrome: a longitudinal clinical study of 32 patients". J Pediatr Endocrinol Metab. 12 (6): 817–26. doi:10.1515/jpem.1999.12.6.817. PMID 10614538.
  9. Frisch LS, Copeland KC, Boepple PA (1992). "Recurrent ovarian cysts in childhood: diagnosis of McCune-Albright syndrome by bone scan". Pediatrics. 90 (1 Pt 1): 102–4. PMID 1614755.
  10. Biermann JS (2002). "Common benign lesions of bone in children and adolescents". J Pediatr Orthop. 22 (2): 268–73. PMID 11856945.
  11. Pichard DC, Boyce AM, Collins MT, Cowen EW (2014). "Oral pigmentation in McCune-Albright syndrome". JAMA Dermatol. 150 (7): 760–3. doi:10.1001/jamadermatol.2014.184. PMC 4933654. PMID 24671640.
  12. Nabhan ZM, West KW, Eugster EA (2007). "Oophorectomy in McCune-Albright syndrome: a case of mistaken identity". J Pediatr Surg. 42 (9): 1578–83. doi:10.1016/j.jpedsurg.2007.04.021. PMID 17848252.
  13. Javaid MK, Boyce A, Appelman-Dijkstra N, Ong J, Defabianis P, Offiah A; et al. (2019). "Best practice management guidelines for fibrous dysplasia/McCune-Albright syndrome: a consensus statement from the FD/MAS international consortium". Orphanet J Rare Dis. 14 (1): 139. doi:10.1186/s13023-019-1102-9. PMC 6567644 Check |pmc= value (help). PMID 31196103.
  14. Ozawa T, Tateishi C, Shirakawa M, Murakami E, Ishii M, Harada T (2011). "Long-term follow-up of a case of cheek hyperpigmentation associated with McCune-Albright syndrome treated with Q-switched ruby laser". Dermatol Surg. 37 (2): 263–6. doi:10.1111/j.1524-4725.2010.01864.x. PMID 21272121.
  15. Chanson P, Salenave S, Orcel P (2007). "McCune-Albright syndrome in adulthood". Pediatr Endocrinol Rev. 4 Suppl 4: 453–62. PMID 17982395.

See also

External links

it:Sindrome di McCune-Albright-Sternberg

Template:WH Template:WikiDoc Sources