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Journal articles on the topic 'Craniofacial fibrous dysplasia'

Author: Grafiati

Published: 2 June 2025

Last updated: 31 July 2025

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1

COŞGUNARSLAN, Aykağan, Mehmet AMUK, Neşe İSPEKTER, and Hatice Cansu KIŞ. "Craniofacial Fibrous Dysplasia." Turkiye Klinikleri Journal of Case Reports 28, no. 2 (2020): 126–32. http://dx.doi.org/10.5336/caserep.2019-72722.

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2

Jhamb, Aakarsh, Sujata Mohanty, and ParulA Jhamb. "Craniofacial fibrous dysplasia." Journal of Oral and Maxillofacial Pathology 16, no. 3 (2012): 465. http://dx.doi.org/10.4103/0973-029x.102523.

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3

Hussein, Mohammed Ahmed, In Sik Yun, Bo Ok Kim, and Yong Oock Kim. "Craniofacial Fibrous Dysplasia." Annals of Plastic Surgery 78, no. 3 (2017): 289–93. http://dx.doi.org/10.1097/sap.0000000000000917.

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4

Zanini, Silvio A., Jorge M. Psillakis, Walter Migowski, and Mark Tershakowec. "Craniofacial Fibrous Dysplasia." Annals of Plastic Surgery 14, no. 4 (1985): 378–82. http://dx.doi.org/10.1097/00000637-198504000-00013.

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5

Camilleri, A. E. "Craniofacial fibrous dysplasia." Journal of Laryngology & Otology 105, no. 8 (1991): 662–66. http://dx.doi.org/10.1017/s0022215100116974.

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AbstractFibrous dysplasia is a benign localized bone disorder of unknown aetiologyin which endocrinopathies, abnormal pigmentation of the skin and mucous membranes may formpart of the disease. Five cases involving the facial and cranial bones are described to illustrate the various presentations and radiological appearances including computerized tomography and magnetic resonance imaging. Some of these cases demonstrate that serial radiology may be adequate for diagnosis and management without the necessity for histological confirmation. The place of limited surgical treatment for the craniofa

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6

Hanifi, Bayarogullari, Kahraman Serif Samil, Cokkeser Yasar, Cevik Cengiz, Akbay Ercan, and Davran Ramazan. "Craniofacial fibrous dysplasia." Clinical Imaging 37, no. 6 (2013): 1109–15. http://dx.doi.org/10.1016/j.clinimag.2013.01.010.

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7

Ricalde, Pat, Kelly R. Magliocca, and Janice S. Lee. "Craniofacial Fibrous Dysplasia." Oral and Maxillofacial Surgery Clinics of North America 24, no. 3 (2012): 427–41. http://dx.doi.org/10.1016/j.coms.2012.05.004.

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8

Mahmoudi Hashemi, Elahe, Mahrokh Imanimoghaddam, Somayeh Nemati, and Zohre Dalir. "Craniofacial Fibrous Dysplasia." Journal of Dentomaxillofacial Radiology, Pathology and Surgery 1, no. 1 (2012): 47–49. http://dx.doi.org/10.18869/acadpub.3dj.1.1.8.

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9

Pruksakorn, Promphan, Shanop Shuangshoti, Rungsak Siwanuwatn, Sukalaya Lerdlum, Sarat Sunthornyothin, and Thiti Snabboon. "Craniofacial Fibrous Dysplasia." Internal Medicine 49, no. 3 (2010): 249–50. http://dx.doi.org/10.2169/internalmedicine.49.2890.

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10

Eversole, Lewis R. "Craniofacial Fibrous Dysplasia and Ossifying Fibroma." Oral and Maxillofacial Surgery Clinics of North America 9, no. 4 (1997): 625–42. http://dx.doi.org/10.1016/s1042-3699(20)30355-1.

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11

Guruprasad, Yadavalli, and Chandan Prabhakar. "Craniofacial polyostotic fibrous dysplasia." Contemporary Clinical Dentistry 1, no. 3 (2010): 177. http://dx.doi.org/10.4103/0976-237x.72787.

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12

Pierce, Angela M., David F. Wilson, and Alastair N. Goss. "Inherited craniofacial fibrous dysplasia." Oral Surgery, Oral Medicine, Oral Pathology 60, no. 4 (1985): 403–9. http://dx.doi.org/10.1016/0030-4220(85)90263-4.

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13

Lello, Glenn E., and Owen C. Sparrow. "Craniofacial polyostotic fibrous dysplasia." Journal of Maxillofacial Surgery 13 (1985): 267–72. http://dx.doi.org/10.1016/s0301-0503(85)80062-x.

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14

Kulakova, G. A., N. A. Solovyeva, E. A. Kurmaeva, et al. "Craniofacial polyossal fibrous dysplasia." Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics) 67, no. 5 (2022): 199–202. http://dx.doi.org/10.21508/1027-4065-2022-67-5-199-202.

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Fibrous dysplasia is a rare anomaly of bone tissue development, in which it is replaced by fibrocystic tissue. A clinical case of a patient with a craniofacial polyossal form of fibrous dysplasia is presented. At the age of 13, a child had a constant intense headache, which was accompanied by dizziness, tinnitus, cognitive impairment, deformity of the frontal region and lower jaw on the right, local pigmentation in the neck and face (coffee-and-milk-like stains). Brain tomography and osteoscintigraphy visualized a volumetric formation in the right half of the skull bones, in which fibrotic dys

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15

International, Journal of Medical Science and Innovative Research (IJMSIR). "Unusual Case of Craniofacial Fibrous Dysplasia." International Journal of Medical Science and Innovative Research (IJMSIR) 9, no. 5 (2024): 34–36. https://doi.org/10.5281/zenodo.15430274.

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<strong>Abstract</strong> Craniofacial fibrous dysplasia is a rare bone disorder characterized by abnormal growth and deformity. We present a case report of a patient with craniofacial fibrous dysplasia, highlighting its radiological features, clinical presentation, and management. The patient demonstrated characteristic ground-glass appearance on CT scans and expansile lesions with sclerotic margins. Surgical intervention and rehabilitation resulted in improved symptom management and quality of life. This case report contributes to the understanding of craniofacial fibrous dysplasia and empha

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16

Gyawali, Bigyan Raj, and Rabindra Bhakta Pradhananga. "Monostotic fibrous dysplasia of temporal bone: a case series and literature review." International Journal of Scientific Reports 6, no. 4 (2020): 167. http://dx.doi.org/10.18203/issn.2454-2156.intjscirep20201273.

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<p>Fibrous dysplasia is a benign, progressive fibro-osseus disease. Typically, there are three variants monostotic, polyostotic and McCune Albright syndrome. Monostotic variant being the commonest of all, affects mainly the craniofacial bones and ribs. Fibrous dysplasia affecting the temporal bone may be challenging at times. Here, we present our case series of three temporal bone fibrous dysplasias along with the literature review.</p>

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17

Lisle, DA, PAJ Monsour, and CD Maskiell. "Imaging of craniofacial fibrous dysplasia." Journal of Medical Imaging and Radiation Oncology 52, no. 4 (2008): 325–32. http://dx.doi.org/10.1111/j.1440-1673.2008.01963.x.

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18

Casselman, J. W., I. De Jonge, L. Neyt, C. De Clercq, and G. D'Hont. "MRI in craniofacial fibrous dysplasia." Neuroradiology 35, no. 3 (1993): 234–37. http://dx.doi.org/10.1007/bf00588505.

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19

Sarihan, Fikret, and Kristel M. Kasius. "Teaching NeuroImages: Craniofacial fibrous dysplasia." Neurology 89, no. 19 (2017): e236-e237. http://dx.doi.org/10.1212/wnl.0000000000004625.

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20

Tabrizi, Reza, and Birkan Taha Özkan. "Craniofacial Fibrous Dysplasia of Orbit." Journal of Craniofacial Surgery 19, no. 6 (2008): 1532–37. http://dx.doi.org/10.1097/scs.0b013e31818ac270.

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21

Forbes-Haley, Claire, Anna Najran, Sukbir Nandra, and Surina Bhola. "Craniofacial polyostotic fibrous dysplasia: A case report." Dental Update 46, no. 8 (2019): 768–74. http://dx.doi.org/10.12968/denu.2019.46.8.768.

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Fibrous dysplasia is a bone disorder whereby normal medullary bone is replaced by fibrous tissue. Many sites may be affected, including the craniofacial skeleton. A 33-year-old female presented at the Bristol Dental Hospital in 2007 complaining of a prominent and expanding lower jaw as well as poor aesthetics. She was diagnosed with craniofacial polyostotic fibrous dysplasia. In order to manage her concerns and the ongoing growth of the polyostotic lesions, a combined maxillofacial and restorative approach was utilized. After ten years of ongoing management and care, including surgery and dent

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22

Rahman, Mohammad Asifur, Tarin Rahman, and Ismat Ara Haider. "Fibro Osseous Lesions of The Craniofacial Structures – A Clinical Study." Update Dental College Journal 8, no. 1 (2018): 45–54. http://dx.doi.org/10.3329/updcj.v8i1.38412.

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Fibro osseous lesions area diverse group of disorders characterized by replacement of normal archi- tecture of bone by a benign connective tissue matrix that displays various amount ofmineralizationin the form of woven bone or cementum. It includes developmental, reactive and neoplastic lesions. The different type of fibro-osseous lesions express a common clinical and radiological features. Soad- equate knowledge and clinical observationare necessary for proper interpretation and appropriate diagnosis of these lesions.becausemanagement of patients with fibro-osseous lesions are case specifican

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23

Unal Erzurumlu, Zerrin, Peruze Celenk, Emel Bulut, and Yakup Sancar Barıs. "CT Imaging of Craniofacial Fibrous Dysplasia." Case Reports in Dentistry 2015 (2015): 1–4. http://dx.doi.org/10.1155/2015/134123.

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Fibrous dysplasia is a benign fibroosseous bone dysplasia that can involve single (monostotic) or multiple (polyostotic) bones. Monostotic form is more frequent in the jaws. It is termed as craniofacial fibrous dysplasia, when it involves, though rarely, adjacent craniofacial bones. A 16-year-old girl consulted for a painless swelling in the right posterior mandible for two years. Panoramic radiography revealed ground-glass ill-defined lesions in the three different regions of the maxilla and mandible. Axial CT scan (bone window) showed multiple lesions involving skull base and facial bones. D

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24

Jain, Sandhya, Vilas Newaskar, and Munira Ali. "Craniofacial Fibrous Dysplasia with Facial Asymmetry, Canted Occlusion and Open Bite: A Case Report with 2 Years Follow-up." Journal of Contemporary Dental Practice 15, no. 5 (2014): 636–45. http://dx.doi.org/10.5005/jp-journals-10024-1592.

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ABSTRACT Aim Fibrous dysplasia is a benign fibro-osseous disorder of unknown etiology that may affect the craniofacial region causing significant impairment of facial esthetics and function. This paper reports a case of a 21-year-old male, which was investigated and diagnosed with craniofacial fibrous dysplasia involving an overgrowth over right maxillary and mandibular region associated with facial asymmetry, severe occlusal cant and anterior open bite. Management of the case included surgical excision, cosmetic contouring and orthodontic intervention. The case was reviewed over a period of t

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25

Ahmed, Bashir, Alok Thakkar, and SM Nurul Irfan. "Optic nerve decompression in Craniofacial fibrous dysplasia involving optic canal: An experience at AIIMS, New Delhi." Bangladesh Journal of Otorhinolaryngology 24, no. 2 (2019): 94–104. http://dx.doi.org/10.3329/bjo.v24i2.44153.

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Background: Gradual progression of craniofacial fibrous dysplasia frequently involves sphenoid and ethmoid bone results encasement of optic canal which leads to visual impairment to complete blindness Methods: Retrospective study was carried out at All India Institute of Medical Sciences on hospital records of 16 cases of craniofacial fibrous dysplasia operated for optic canal involvement with or without visual impairment with an objective to discuss about the indications, suitable timing and outcome of optic nerve decompression in cases of optic canal involvement. Results: Out of

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26

Joseph, Sara, Matteo, Alessandro, and Caterina. "Craniofacial Fibrous Dysplasia: Diagnosis and Treatment Options." Proceedings 35, no. 1 (2019): 59. http://dx.doi.org/10.3390/proceedings2019035059.

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27

Mehra, Garima, Gaurav Agarwal, and Madhvi Savelkar. "Craniofacial fibrous dysplasia of the maxilla: A case report." International Journal of Oral Health Dentistry 10, no. 4 (2024): 296–300. https://doi.org/10.18231/j.ijohd.2024.052.

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Fibrous dysplasia (FD) is an asymptomatic local alteration of bone in which the typical architecture is replaced by fibrous tissues and nonfunctional trabeculae like osseous structures. The lesion most frequently affects the craniofacial skeleton. The maxilla is affected twice compared to the mandible and occurs more commonly in the posterior area. An unusual fibrous dysplasia involving a female's left craniofacial region is reported. The clinical features, radiological findings and treatment have been discussed. Bisphosphonate therapy may help improve function for treatment; surgery is indica

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28

Lee, Seong Suk, Ghi Jai Lee, Myung Seok Jung, Yong Soo Kim, Ho Kyun Kim, and Chang Yul Han. "CT findings of craniofacial fibrous dysplasia." Journal of the Korean Radiological Society 29, no. 6 (1993): 1260. http://dx.doi.org/10.3348/jkrs.1993.29.6.1260.

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29

AYKAN, Andac, Serbulent GZEY, Fatih ZOR, Bulent DZ, Ali CICEK, and Serdar OZTRK. "Craniofacial Fibrous Dysplasia: A Case Report." Gulhane Medical Journal 57, no. 4 (2015): 430. http://dx.doi.org/10.5455/gulhane.47670.

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30

Agrawal, Siddharth, and RajatM Srivastava. "Craniofacial fibrous dysplasia with ipsilateral keratoconus." Journal of Clinical Ophthalmology and Research 8, no. 2 (2020): 78. http://dx.doi.org/10.4103/jcor.jcor_83_19.

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31

Lai, Wen-Sen, and Jih-Chin Lee. "Fibrous Dysplasia of the Craniofacial Bones." Journal of the American Osteopathic Association 113, no. 8 (2013): 641. http://dx.doi.org/10.7556/jaoa.2013.027.

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32

Faul, S., J. Link, S. Behrendt, and R. Rochels. "MRI features of craniofacial fibrous dysplasia." Orbit 17, no. 2 (1998): 125–32. http://dx.doi.org/10.1076/orbi.17.2.125.2759.

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33

Holl, Dana C., Jose A. U. Hardillo, Ruben Dammers, Marc P. van der Schroeff, and Aad van der Lugt. "Cystic Degeneration of Craniofacial Fibrous Dysplasia." World Neurosurgery 120 (December 2018): 159–62. http://dx.doi.org/10.1016/j.wneu.2018.08.175.

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34

BORDIGNON, NATÁLIA CRISTINA TRENTIN, LUIZ HENRIQUE GODOI MAROLA, and ROGÉRIO DE OLIVEIRA GONDAK. "CRANIOFACIAL FIBROUS DYSPLASIA: A CASE REPORT." Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology 130, no. 3 (2020): e125. http://dx.doi.org/10.1016/j.oooo.2020.04.074.

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35

SILVA, MAIZA LUIZA VIEIRA, TÂNIA MARA PIMENTA AMARAL, MARIA BEATRIZ PIRES DE MAGALHÃES, HENRIQUE PRETTI, and RICARDO ALVES MESQUITA. "Craniofacial Fibrous Dysplasia in Pediatric Patient." Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology 117, no. 2 (2014): e151. http://dx.doi.org/10.1016/j.oooo.2013.11.097.

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36

Moya Sánchez, E., and Á. Ruiz de Arévalo García. "Craniofacial polyostotic fibrous dysplasia: Imaging findings." Radiología (English Edition) 61, no. 2 (2019): 177–78. http://dx.doi.org/10.1016/j.rxeng.2018.11.006.

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37

Nikbin, Ava, Seiedeh Tahereh Mohtavipour, Alieh Sadat Javadzadeh Haghighat, Saeed dashtyari, and Mohammad Talebzadeh. "Craniofacial fibrous dysplasia: New image findings." Journal of Dentomaxillofacial Radiology, Pathology and Surgery 5, no. 4 (2017): 26–27. http://dx.doi.org/10.18869/acadpub.3dj.5.4.26.

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38

L.R, DrVaibhav, DrSindhu Ravindra, DrSowmya Krishna, DrK VRama Krishna, Drkollapuri Sarath, and DrDeepak T.A. "CRANIOFACIAL FIBROUS DYSPLASIA: A CASE REPORT." International Journal of Advanced Research 4, no. 7 (2016): 1704–7. http://dx.doi.org/10.21474/ijar01/961.

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39

Leong, Leonard Tang Yew, and Benjamin Julian Chang Chong Ming. "Craniofacial Fibrous Dysplasia Involving the Orbit." Asia-Pacific Journal of Ophthalmology 4, no. 3 (2015): 151–54. http://dx.doi.org/10.1097/apo.0000000000000043.

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40

Clauser, Luigi, Claudio Marchetti, Massimo Piccione та Franco Bertoni. "Craniofacial Fibrous Dysplasia and Ollierʼs Disease". Journal of Craniofacial Surgery 7, № 2 (1996): 140–43. http://dx.doi.org/10.1097/00001665-199603000-00012.

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41

Dubois, L., R. Schreurs, P. Saeed, and A. G. Becking. "Craniofacial fibrous dysplasia: current treatment options." International Journal of Oral and Maxillofacial Surgery 46 (March 2017): 16. http://dx.doi.org/10.1016/j.ijom.2017.02.057.

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42

Kim, Dong Yeon. "Current concepts of craniofacial fibrous dysplasia: pathophysiology and treatment." Archives of Craniofacial Surgery 24, no. 2 (2023): 41–51. http://dx.doi.org/10.7181/acfs.2023.00101.

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Fibrous dysplasia is an uncommon genetic disorder in which bone is replaced by immature bone and fibrous tissue, manifesting as slowgrowing lesions. Sporadic post-zygotic activating mutations in GNAS gene result in dysregulated GαS-protein signaling and elevation of cyclic adenosine monophosphate in affected tissues. This condition has a broad clinical spectrum, ranging from insignificant solitary lesions to severe disease. The craniofacial area is the most common site of fibrous dysplasia, and nine out of 10 patients with fibrous dysplasia affecting the craniofacial bones present before the a

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43

Bhosale, Alisha, Pooja Upase, and Joshna Choudhary. "Fibrous Dysplasia - A Rare Case Presentation." International Journal of Research and Review 11, no. 6 (2024): 636–39. http://dx.doi.org/10.52403/ijrr.20240670.

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A developmental benign medullary fibro-osseous process known as fibrous dysplasia (FD) is typified by the failure to create mature lamellar bone and a stoppage as woven bone, which may be multifocal. Fibrous dysplasia is a rare condition that can affect people of any age in both adults and children. Typically, young adults and children receive the initial diagnosis. Although the actual frequency is unknown, it is thought to account for about 5% of benign bone lesions. This exercise looks at how fibrous dysplasia should be evaluated and emphasizes the need of a multidisciplinary approach in pro

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44

Sachdev, Sanpreet Singh, Tabita Joy Chettiankandy, Manisha Ahire Sardar, Ashish Sarda, and Ashwini Chhapane. "The histological artistry of fibrous dysplasia: A case report." IP Archives of Cytology and Histopathology Research 7, no. 4 (2022): 273–76. http://dx.doi.org/10.18231/j.achr.2022.064.

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Fibrous dysplasia (FD) is a fibro-osseous lesion characterized by the replacement of normal medullary bone by proliferative fibrous connective tissue. It comprises only 2% of all benign tumors and tumor-like processes of the bone. Craniofacial FD can occur in monostotic or polyostotic forms, and in conjunction with other endocrinal abnormalities. The monostotic FD is of particular importance for dental professionals owing to its propensity to occur in the jawbones. Differentiating FD from other fibro-osseous lesions such as ossifying fibroma and cemento-osseous dysplasia requires a fair amount

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45

Durugkar, Mrunmayee Shrikant, Mahendra Ramdas Patait, Kedar Saraf, Misbah Farheen Mulla, Suyog Tupsakhare, and Swati Jadhav. "Craniofacial fibrous dyplasia: A case report with emphasis on radiographic findings." Journal of Oral Medicine, Oral Surgery, Oral Pathology and Oral Radiology 8, no. 4 (2022): 226–31. http://dx.doi.org/10.18231/j.jooo.2022.047.

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Fibrous dysplasia (FD) is an idiopathic skeletal disorder where normal bone gets replaced by poorly organized fibrous connective tissue. The lesion is classified into two forms: monostotic and polyostotic. This disorder arises from sporadic mutation of the α-subunit of the Gs stimulatory protein. Although histopathology is a gold standard in the diagnosis of any pathology, radiology remains an important investigation. In radiology, fibrous dysplasia is very often associated with the term ground glass matrix. The knowledge of its unique pathogenesis and course are crucial to understand imaging

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46

Miranda, Poliana Gonçalves, João César Guimaraes Henriques, Luiz Fernando Barbosa de Paulo, Cizelene do Carmo Faleiros Veloso Guedes, Fabio Franceschini Mitri, and Cláudia Jordão Silva. "Jaffe-Lichtenstein Syndrome Associated with a Simple Bone Cyst: Unprecedented Rare Case Report." Brazilian Dental Journal 31, no. 5 (2020): 557–61. http://dx.doi.org/10.1590/0103-6440202003158.

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Abstract Lesions denominated fibro-osseous lesions of the jaw constitute a diversified group of disorders, in which the normal bone architecture is replaced by fibroblasts, collagen fibers and immature bone. At present, the World Health Organization recognizes four variants of these lesions, namely: bone-cement dysplasia, fibrous dysplasia, ossifying fibroma and Familial gigantiform cementoma. Fibrous dysplasia may present in the monostotic form, affecting one single bone or an isolated craniofacial region; and in the Polyostotic form, involving two or more bones of the skeleton, and eventual

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47

Levy, Michael L., Thomas C. Chen, and Martin H. Weiss. "Monostotic fibrous dysplasia of the clivus." Journal of Neurosurgery 75, no. 5 (1991): 800–803. http://dx.doi.org/10.3171/jns.1991.75.5.0800.

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✓ A case report of monostotic fibrous dysplasia of the clivus in a postadolescent woman is described. Although fibrous dysplasia of craniofacial structures is well documented, involvement of the clivus has not been reported. Diagnosis by clinical, radiographic, and histopathological features is detailed. Implications for the role of surgery and management are discussed.

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48

Ossouka, Nadiha, Hanane EL Mouden, ELouali Aicha, et al. "Orbital Cellulitis Revealing a Craniofacial Fibrous Dysplasia." SAS Journal of Medicine 7, no. 12 (2021): 717–19. http://dx.doi.org/10.36347/sasjm.2021.v07i12.015.

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Fibrous bone dysplasia (FOD) is a benign, rare, congenital condition, underestimated because it is often asymptomatic, and of unknown cause. It is a disease in which normal bone is replaced by fibro-osseous tissue resulting in deforming bone lesions. The disease is most often monostotic, much more rarely polyostotic. We report an observation of a 10-year-old female patient who presented with a painful periorbital swelling initially labeled as orbital cellulitis. Orbital CT confirmed bilateral orbital cellulitis but also made the diagnosis of craniofacial fibrous dysplasia on the bony windows.

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49

Menon, Suresh, Srihari Venkatswamy, Veena Ramu, Khurshida Banu, Sham Ehtaih, and VinayM Kashyap. "Craniofacial fibrous dysplasia: Surgery and literature review." Annals of Maxillofacial Surgery 3, no. 1 (2013): 66. http://dx.doi.org/10.4103/2231-0746.110088.

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50

Neelima, Chembolu, PatlolaBal Reddy, Chembolu Nirupama, and EndlaVarun Kumar. "Priority of treatment in craniofacial fibrous dysplasia." Annals of Maxillofacial Surgery 9, no. 2 (2019): 451. http://dx.doi.org/10.4103/ams.ams_186_17.

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