Generic placeholder image

Current Medical Imaging

Editor-in-Chief

ISSN (Print): 1573-4056
ISSN (Online): 1875-6603

General Review Article

Craniofacial Fibrous Dysplasia Involvements of Mccune-Albright Syndrome: A Review with an Additional Case

Author(s): İlknur Özcan, Gürkan Ünsal, Revan Birke Koca* and Kaan Orhan

Volume 17, Issue 7, 2021

Published on: 09 December, 2020

Page: [864 - 870] Pages: 7

DOI: 10.2174/1573405616666201209102418

Price: $65

Abstract

Background: McCune-Albright Syndrome (MAS) is a genetic disorder with a triad of endocrine diseases, café-au-lait macules and fibrous dysplasias. Craniofacial fibrous dysplasia is a term that is used to describe the fibrous dysplasia, which was localized at the craniofacial skeleton and is common in MAS patients.

Objective: The objective of this review is to determine the involvement frequency of cranial and facial bones in patients with MAS and CFD.

Methods: Articles in PubMed was searched with the following details “(mccune[Title/Abstract] OR albright[Title/Abstract]) OR (“craniofacial fibrous dysplasia”[MeSH Terms] OR (“craniofacial”[ All Fields] AND “fibrous”[All Fields] AND “dysplasia”[All Fields]) OR “craniofacial fibrous dysplasia”[All Fields])”. The articles in which the authors did not state the involved bones or did not add any radiographic images were excluded from the study.

Results: 26 cases in 25 articles met the inclusion criteria. Among the 26 cases and our case, sphenoid and frontal bones were involved in 17 cases, parietal and occipital bones were involved in 15 cases, mandible and ethmoid bone were involved in 14 cases, maxilla-zygoma-temporal and palate was involved in 13, 11, 6 and 3 cases, respectively. Palate was involved in cases where maxilla was also involved. Our case was the only case that was evaluated with CBCT.

Conclusion: Routine follow-ups are important since new CFDs can occur in different cranial or facial bones. 2D imaging techniques may not be able to demonstrate early CFDs; thus, an advanced imaging technique should be used after MAS diagnosis.

Keywords: Craniofacial fibrous dysplasia, polyostotic fibrous dysplasia, cafe-au-Lait spots, cone-beam computed tomography, panoramic radiography, MAS(McCune-Albright syndrome).

Graphical Abstract

[1]
Spencer T, Pan KS, Collins MT, Boyce AM. The clinical spectrum of McCune-Albright syndrome and its management. Horm Res Paediatr 2019; 92(6): 347-56.
[http://dx.doi.org/10.1159/000504802] [PMID: 31865341]
[2]
Takayasu S, Makita K, Kageyama K, et al. Presence of aberrant adrenocorticotropic hormone precursors in two cases of McCune-Albright syndrome. Endocr J 2019.
[PMID: 31801917]
[3]
Kelly MH, Brillante B, Collins MT. Pain in fibrous dysplasia of bone: Age-related changes and the anatomical distribution of skeletal lesions. Osteoporos Int 2008; 19(1): 57-63.
[http://dx.doi.org/10.1007/s00198-007-0425-x] [PMID: 17622477]
[4]
Burke AB, Collins MT, Boyce AM. Fibrous dysplasia of bone: craniofacial and dental implications. Oral Dis 2017; 23(6): 697-708.
[http://dx.doi.org/10.1111/odi.12563] [PMID: 27493082]
[5]
Hansen MR, Moffat JC. Osteosarcoma of the skull base after radiation therapy in a patient with McCune-Albright syndrome: Case report. Skull Base 2003; 13(2): 79-83.
[http://dx.doi.org/10.1055/s-2003-40597] [PMID: 15912163]
[6]
Kanazawa I, Yamauchi M, Yano S, et al. Osteosarcoma in a pregnant patient with McCune-Albright syndrome. Bone 2009; 45(3): 603-8.
[http://dx.doi.org/10.1016/j.bone.2009.05.018] [PMID: 19481621]
[7]
Sung SH, Yoon HD, Shon HS, et al. A case of McCune-Albright syndrome with associated multiple endocrinopathies. Korean J Intern Med (Korean Assoc Intern Med) 2007; 22(1): 45-50.
[http://dx.doi.org/10.3904/kjim.2007.22.1.45] [PMID: 17427647]
[8]
Dumitrescu CE, Collins MT. McCune-Albright syndrome. Orphanet J Rare Dis 2008; 3: 12.
[http://dx.doi.org/10.1186/1750-1172-3-12] [PMID: 18489744]
[9]
Li P, Zhang ZR, Jiang Y, Xia XD, Wang D, Li XF. MR and CT findings of cyst degeneration of sphenoid bone in McCune-Albright syndrome: A case report. Cases J 2009; 2: 9376.
[http://dx.doi.org/10.1186/1757-1626-2-9376] [PMID: 20062549]
[10]
Rostampour N, Hashemipour M, Kelishadi R, Hovsepian S, Hekmatnia A. A case of atypical McCune-Albright syndrome with vaginal bleeding. Iran J Pediatr 2011; 21(3): 399-403.
[PMID: 23056821]
[11]
Liu F, Li W, Yao Y, et al. A case of McCune-Albright syndrome associated with pituitary GH adenoma: Therapeutic process and autopsy. J Pediatr Endocrinol Metab 2011; 24(5-6): 283-7.
[PMID: 21823524]
[12]
Classen CF, Mix M, Kyank U, Hauenstein C, Haffner D. Pamidronic acid and cabergoline as effective long-term therapy in a 12-year-old girl with extended facial polyostotic fibrous dysplasia, prolactinoma and acromegaly in McCune-Albright syndrome: A case report. J Med Case Reports 2012; 6: 32.
[http://dx.doi.org/10.1186/1752-1947-6-32] [PMID: 22273876]
[13]
Chakraborty D, Mittal BR, Kashyap R, Manohar K, Bhattacharya A, Bhansali A. Radioiodine treatment in McCune-Albright syndrome with hyperthyroidism. Indian J Endocrinol Metab 2012; 16(4): 654-6.
[http://dx.doi.org/10.4103/2230-8210.98035] [PMID: 22837937]
[14]
Genç DB, Özkan MA, Büyükgebiz A. McCune-Albright syndrome mimicking malignancy: An endocrine disease from oncologist’s perspective. J Clin Res Pediatr Endocrinol 2012; 4(3): 160-3.
[http://dx.doi.org/10.4274/Jcrpe.712] [PMID: 22985616]
[15]
Akintoye SO, Boyce AM, Collins MT. Dental perspectives in fibrous dysplasia and McCune-Albright syndrome. Oral Surg Oral Med Oral Pathol Oral Radiol 2013; 116(3): e149-55.
[http://dx.doi.org/10.1016/j.oooo.2013.05.023] [PMID: 23953425]
[16]
Kollerova J, Koller T, Zelinkova Z, Kostalova L, Payer J. Treatment of pathological bone fractures in a patient with McCune-Albright syndrome. Case Rep Endocrinol 2013; 2013589872
[http://dx.doi.org/10.1155/2013/589872] [PMID: 24369512]
[17]
DeKlotz TR, Kim HJ, Kelly M, Collins MT. Sinonasal disease in polyostotic fibrous dysplasia and McCune-Albright Syndrome. Laryngoscope 2013; 123(4): 823-8.
[http://dx.doi.org/10.1002/lary.23758] [PMID: 23444264]
[18]
Aravinda K, Ratnakar P, Srinivas K. Oral manifestations of McCune-Albright syndrome. Indian J Endocrinol Metab 2013; 17(1): 170-3.
[http://dx.doi.org/10.4103/2230-8210.107878] [PMID: 23776876]
[19]
Jung KE, Lee JH, Kim TY. A suspected case and literature review of McCune-Albright syndrome. Ann Dermatol 2014; 26(5): 639-40.
[http://dx.doi.org/10.5021/ad.2014.26.5.639] [PMID: 25324661]
[20]
Shetty S, Varghese RT, Shanthly N, Paul TV. Toxic thyroid adenoma in McCune-Albright syndrome. J Clin Diagn Res 2014; 8(2): 281-2.
[PMID: 24701557]
[21]
Noh JH, Kong DS, Seol HJ, Shin HJ. Endoscopic decompression for optic neuropathy in McCune-Albright syndrome. J Korean Neurosurg Soc 2014; 56(3): 281-3.
[http://dx.doi.org/10.3340/jkns.2014.56.3.281] [PMID: 25368777]
[22]
Xu J, Li X, Lv CS, et al. Treatment protocols for growth hormone-secreting pituitary adenomas combined with craniofacial fibrous dysplasia: A case report of atypical McCune-Albright syndrome. Exp Ther Med 2014; 8(3): 877-80.
[http://dx.doi.org/10.3892/etm.2014.1792] [PMID: 25120617]
[23]
Williams RG. A case of craniofacial fibrous dysplasia associated with McCune-Albright syndrome lost to follow-up. BMJ Case Rep 2015.
[http://dx.doi.org/10.1136/bcr-2014-209011]
[24]
Özsu E, Mutlu GY, Çizmecioğlu FM, Hatun Ş. McCune Albright syndrome in association with excessive GH secretion: Case report. Turk Pediatri Ars 2015; 50(2): 114-7.
[http://dx.doi.org/10.5152/tpa.2015.615] [PMID: 26265896]
[25]
Belsuzarri TA, Araujo JF, Melro CA, et al. McCune-Albright syndrome with craniofacial dysplasia: Clinical review and surgical management. Surg Neurol Int 2016; 7(Suppl. 6): S165-9.
[http://dx.doi.org/10.4103/2152-7806.178567] [PMID: 27057395]
[26]
Wójcik S, Koszowski R, Drozdowska B, Śmieszek-Wilczewska J, Raczkowska-Siostrzonek A. Maxillary fibrous dysplasia associated with McCune-Albright syndrome. A case study. Open Med (Wars) 2016; 11(1): 465-70.
[http://dx.doi.org/10.1515/med-2016-0082] [PMID: 28352837]
[27]
Tournis S, Balanika A, Megaloikonomos PD, Mavrogenis AF. Secondary aneurysmal bone cyst in McCune-Albright syndrome. Clin Cases Miner Bone Metab 2017; 14(3): 332-5.
[http://dx.doi.org/10.11138/ccmbm/2017.14.3.332] [PMID: 29354163]
[28]
Kumar N, Kheruka SC, Singh RK, Ravina M, Dutta D, Gambhir S. Hypothyroidism in McCune-Albright syndrome and role of bone scan in management of fibrous dysplasia: An unusual case scenario with review of literature. Indian J Nucl Med 2017; 32(1): 25-9.
[http://dx.doi.org/10.4103/0972-3919.198462] [PMID: 28242980]
[29]
Pal R, Dutta P, Mukherjee KK, et al. Acromegaly with hypophosphataemia: McCune-Albright syndrome. BMJ Case Rep 2017.
[30]
Pina Rivera Y, Rwegerera GM, Sesay S. Short stature and growth hormone deficiency: unexpected manifestations of McCune-Albright syndrome. BMJ Case Rep 2018.
[http://dx.doi.org/10.1136/bcr-2018-225709]
[31]
Boyce AM, Florenzano P, de Castro LF, et al. Fibrous dysplasia/McCune-Albright syndrome. GeneReviews((R)). Seattle, WA 1993.
[32]
Dean L. McCune-Albright syndrome.Medical genetics summaries. Bethesda, MD 2012.
[33]
Leet AI, Chebli C, Kushner H, et al. Fracture incidence in polyostotic fibrous dysplasia and the McCune-Albright syndrome. J Bone Miner Res 2004; 19(4): 571-7.
[http://dx.doi.org/10.1359/JBMR.0301262] [PMID: 15005844]
[34]
Szabo BT, Aksoy S, Repassy G, Csomo K, Dobo-Nagy C, Orhan K. Comparison of hand and semiautomatic tracing methods for creating maxillofacial artificial organs using sequences of computed tomography (CT) and cone beam computed tomography (CBCT) images. Int J Artif Organs 2017; 40(6): 307-12.
[http://dx.doi.org/10.5301/ijao.5000580] [PMID: 28525668]
[35]
Cakir Karabas H, Ozcan I, Erturk AF, Guray B, Unsal G, Senel SN. Cone-beam computed tomography evaluation of impacted and transmigrated mandibular canines: A retrospective study. Oral Radiol 2020.
[http://dx.doi.org/10.1007/s11282-020-00464-9] [PMID: 32632702]
[36]
White SC, Pharoah MJ. Oral Radiology: Principles and Interpretation. 7th ed. Elsevier Inc. 2014.
[37]
Jibbe N, Jibbe A, Rajpara A. McCune Albright Syndrome. Kans J Med 2020; 13: 49-50.
[http://dx.doi.org/10.17161/kjm.v13i1.13491] [PMID: 32190188]

Rights & Permissions Print Cite
© 2024 Bentham Science Publishers | Privacy Policy