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Journal articles on the topic 'Cherubism'

Author: Grafiati

Published: 4 June 2021

Last updated: 16 February 2022

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1

Etoz, Osman A., Dogan Dolanmaz, and Omer Gunhan. "Treatment of Cherubism with Salmon Calcitonin: A Case Report." European Journal of Dentistry 05, no. 04 (2011): 486–91. http://dx.doi.org/10.1055/s-0039-1698923.

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ABSTRACTCherubism is a familial disease of the jaws which is inherited via autosomal dominant manner. Typical features of cherubism include a painless bilateral, symmetrical enlargement of the jaws, misalignment of teeth, and intra-osseous central giant cell granuloma-like lesions, which are usually evident in early childhood. Treatment of cherubism consists of local curettage of the lesions, jaw contouring, intralesional steroid injections, and systemic calcitonin administration as well. Calcitonin therapy for central giant cell granuloma of the jaws is well documented, and favorable results

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2

Hiremath, Dr Mallayya C., Dr SK Srinath, Dr Bineesh Balan, and Dr Sushma H S. "Cherubism in a 12-year old Child; A Rare Case Report." RGUHS Journal of Dental Sciences 12, no. 2 (2020): 39–42. http://dx.doi.org/10.26715/rjds.12_2_8.

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Cherubism is a non-neoplastic, fibro-osseous, self-limiting, autosomal dominant disorder of the jaws. It is also called as familial fibrous dysplasia and familial multi-locular cystic lesion of the jaws. Its typical dento-facial deformities are caused by mutations in the SH3BP2 gene. The lesion regresses during puberty and the disease stabilizes after the growth period. But it leaves some facial deformity along with disturbances in occlusion. Cherubism may occur as an individual case or in multiple members of the same family, oftenly in multiple generations. Radiographic examination of the les

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3

Chomette, G., M. Auriol, F. Guilbert, and J. M. Vaillant. "Cherubism." International Journal of Oral and Maxillofacial Surgery 17, no. 4 (1988): 219–23. http://dx.doi.org/10.1016/s0901-5027(88)80043-2.

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4

Zachariades, Nicholas, Stavros Papanicolaou, Assimina Xypolyta, and Ioannis Constantinidis. "Cherubism." International Journal of Oral Surgery 14, no. 2 (1985): 138–45. http://dx.doi.org/10.1016/s0300-9785(85)80085-5.

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5

Riefkohl, Ronald, Gregory S. Georgiade, and Nicholas G. Georgiade. "Cherubism." Annals of Plastic Surgery 14, no. 1 (1985): 85–90. http://dx.doi.org/10.1097/00000637-198501000-00016.

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6

Vaillant, Jean-Marie, Pascal Romain, and Marc Divaris. "Cherubism." Journal of Cranio-Maxillofacial Surgery 17, no. 8 (1989): 345–49. http://dx.doi.org/10.1016/s1010-5182(89)80103-9.

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7

Shokri, Abbas, and Atefeh Khavid. "Cherubism." Journal of Craniofacial Surgery 27, no. 5 (2016): e511-e512. http://dx.doi.org/10.1097/scs.0000000000002768.

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8

Khalifa, M. C., and R. A. Ibrahim. "Cherubism." Journal of Laryngology & Otology 102, no. 6 (1988): 568–70. http://dx.doi.org/10.1017/s0022215100105717.

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9

Hitomi, Gonjiro, Naoto Nishide, and Kazuei Mitsui. "Cherubism." Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontology 81, no. 5 (1996): 623–28. http://dx.doi.org/10.1016/s1079-2104(96)80060-6.

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10

Mohan, R. P. S., S. Verma, U. Singh, and N. Agarwal. "Cherubism." Case Reports 2013, jul03 1 (2013): bcr2013010366. http://dx.doi.org/10.1136/bcr-2013-010366.

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11

Temtamy, Samia A., Ahmad F. Abd El Azeem, Tarek H. El Badry, Mennat Allah I. Mehrez, and Marwa El Kassaby. "Cherubism." Middle East Journal of Medical Genetics 1, no. 1 (2012): 53–56. http://dx.doi.org/10.1097/01.mxe.0000407740.11109.d8.

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12

Al-Omar, Ahmed F., Basma G. Moussa, and Usama Abd El Raouf M. El-Dakrory. "Cherubism." Egyptian Journal of Oral & Maxillofacial Surgery 6, no. 2 (2015): 62–65. http://dx.doi.org/10.1097/01.omx.0000462787.66530.51.

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13

Thompson, Lester D. R. "Cherubism." Ear, Nose & Throat Journal 94, no. 1 (2015): E—22—E—24. http://dx.doi.org/10.1177/014556131509400107.

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14

Pal, Rimesh, and Pinaki Dutta. "Cherubism." Indian Pediatrics 57, no. 6 (2020): 595–96. http://dx.doi.org/10.1007/s13312-020-1879-6.

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15

Kömerik, Nurgül, Betül Taş, and Levent Önal. "Cherubism." Head and Neck Pathology 8, no. 2 (2013): 164–67. http://dx.doi.org/10.1007/s12105-013-0489-1.

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16

Chakrabarti, A. K., B. K. Kundu, and S. Ghosh. "Cherubism." Indian Journal of Otolaryngology and Head and Neck Surgery 47, no. 4 (1995): 315–17. http://dx.doi.org/10.1007/bf03048000.

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17

Gupta, Neelima, P. P. Singh, and Usha Rani Singh. "Cherubism." Indian Journal of Otolaryngology and Head and Neck Surgery 54, no. 3 (2002): 229–31. http://dx.doi.org/10.1007/bf02993110.

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18

Imai, Yoshimichi, Kiyoshi Kanno, Takuya Moriya, et al. "A Missense Mutation in the SH3BP2 Gene on Chromosome 4p16.3 Found in a Case of Nonfamilial Cherubism." Cleft Palate-Craniofacial Journal 40, no. 6 (2003): 632–38. http://dx.doi.org/10.1597/1545-1569_2003_040_0632_ammits_2.0.co_2.

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Objective Cherubism is a rare hereditary multilocular cystic disease of the jaws, characterized by its typical appearance. Although nonfamilial cases have been reported, it is difficult to distinguish nonfamilial cherubism from central giant cell granuloma. Recent studies have revealed the point mutations in the SH3BP2 gene on chromosome 4p16.3 in cherubism families. In this article, the SH3BP2 gene in nonfamilial cherubism was examined. Patient A 21-year-old Japanese woman with nonfamilial cherubism. Interventions Genomic DNA was purified from a blood sample obtained from the patient and used

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19

Irfan, S., A. Cassels-Brown, J. M. Hayward, and A. M. Corrigan. "Orbital cherubism." Orbit 16, no. 2 (1997): 109–12. http://dx.doi.org/10.3109/01676839709019125.

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20

Trivedi, A., S. Sharma, R. Mehta, and SD Gupta. "Nonfamilial cherubism." Journal of Indian Society of Pedodontics and Preventive Dentistry 31, no. 1 (2013): 43. http://dx.doi.org/10.4103/0970-4388.112408.

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21

Singh, Anurag, Nidhee Chandra, and Arun Sharma. "Non-familial cherubism." Contemporary Clinical Dentistry 2, no. 2 (2011): 131. http://dx.doi.org/10.4103/0976-237x.83076.

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22

Prajapati, VirendraKumar. "Non-familial Cherubism." Contemporary Clinical Dentistry 4, no. 1 (2013): 88. http://dx.doi.org/10.4103/0976-237x.111609.

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23

Niranjan, Babita, ND Shashikiran, Shilpy Singla, and Sowmya Kasetty. "Non-hereditary cherubism." Journal of Oral and Maxillofacial Pathology 18, no. 1 (2014): 84. http://dx.doi.org/10.4103/0973-029x.131920.

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24

Stiller, Michael, Maik Urban, Werner Golder, et al. "Craniosynostosis in cherubism." American Journal of Medical Genetics 95, no. 4 (2000): 325–31. http://dx.doi.org/10.1002/1096-8628(20001211)95:4<325::aid-ajmg6>3.0.co;2-r.

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25

WELLS, ROBERT G., and JOHN R. STY. "Bone Scintigraphy Cherubism." Clinical Nuclear Medicine 10, no. 12 (1985): 892. http://dx.doi.org/10.1097/00003072-198512000-00018.

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26

Fernández, MC, MS Parisi, and B. Oliveri. "Persistence of cherubism." Bone 40, no. 3 (2007): S15. http://dx.doi.org/10.1016/j.bone.2006.12.044.

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27

Yamaguchi, Takehiko, H. D. Dorfman, and Sidney Eisig. "Cherubism: clinicopathologic features." Skeletal Radiology 28, no. 6 (1999): 350–53. http://dx.doi.org/10.1007/s002560050530.

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28

E. Gentili, Marc, Edwige Levreil, and Nicolas Bedhet. "Cherubism and anaesthesia." Anaesthesiology Intensive Therapy 53, no. 3 (2021): 286–87. http://dx.doi.org/10.5114/ait.2021.105980.

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29

Karbasi Kheir, Mitra. "Case Report of Nonfamilial Cherubism in a Toddler: Description of Clinic-Radiographic Features and Osseous-Dental Treatments." Case Reports in Medicine 2016 (2016): 1–5. http://dx.doi.org/10.1155/2016/8795765.

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Cherubism is a rare familial disease that occurs between the ages two and five years and regresses after puberty. Most of the cherubism cases show familial history, but there are some cases without familial histories of disorder. A two-year-old boy with a painless symmetrical progressive swelling of the jaws had visited maxillofacial radiology department. Panoramic radiograph revealed well-defined multilocular, radiolucent areas of both jaws. Computed tomography of the jaws showed well-defined, bilateral, multilocular, expansile lesions with thinning of cortical plate of maxilla and mandible a

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30

Reddy, GV, G. Siva Prasad Reddy, NVS Sekhar Reddy, and Raj Kumar Badam. "Aggressive Form of Cherubism." Journal of Clinical Imaging Science 2 (February 25, 2012): 8. http://dx.doi.org/10.4103/2156-7514.93275.

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Cherubism is a rare non-neoplastic hereditary disease related to genetic mutations characterized by symmetrically swollen cheeks, particularly over the angles of the mandible, and an upward turning of the eyes. The affected mandible and maxilla begin to swell in early childhood, and gradually increase until the age of puberty. Apparently, surgical intervention is unnecessary unless significant functional, esthetic, or emotional disturbances develop. In the present paper, we report a case of cherubism, with classic features that was classified as grade 3, managed with surgery and followed up fo

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31

Kawamura, Haruka, Satoshi Watanabe, Takashi I, Izumi Asahina, Hiroyuki Moriuchi, and Sumito Dateki. "Efficacy and safety of denosumab treatment in a prepubertal patient with cherubism." Journal of Pediatric Endocrinology and Metabolism 33, no. 7 (2020): 963–66. http://dx.doi.org/10.1515/jpem-2019-0581.

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AbstractBackgroundDenosumab is an inhibitor of receptor activator of nuclear factor kappa-B ligand, which strongly suppresses osteoclasts. Cherubism is a rare autosomal dominant disorder characterized by symmetrical swelling of the jaws, in which the bone is replaced by a fibrous granuloma containing osteoclast-like giant cells.Case presentationWe report the efficacy and safety of denosumab treatment in a prepubertal boy with progressive cherubism. The treatment consisting of eight subcutaneous denosumab injections (120 mg/dose) in 6 months not only suppressed the expansion of the osteolytic l

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32

Beaman, Francesca D., Laura W. Bancroft, Jeffrey J. Peterson, Mark J. Kransdorf, Mark D. Murphey, and David M. Menke. "Imaging Characteristics of Cherubism." American Journal of Roentgenology 182, no. 4 (2004): 1051–54. http://dx.doi.org/10.2214/ajr.182.4.1821051.

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33

Jasuja, Purshottam. "Cherubism: A Case Report." International Journal of Clinical Pediatric Dentistry 2, no. 3 (2009): 49–52. http://dx.doi.org/10.5005/jp-journals-10005-1019.

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34

YAMAGA, Ken, Tadamitsu KAMEYAMA, Seiji ESAKI, Shunichi TANAKA, and Chokudo SUJAKU. "A case of cherubism." Japanese Journal of Oral & Maxillofacial Surgery 36, no. 8 (1990): 1976–80. http://dx.doi.org/10.5794/jjoms.36.1976.

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35

Singh, Priya, Abhinav Singh, and M. Srinivasa Raju. "Cherubism: A case report." International Journal of Case Reports and Images 4, no. 5 (2013): 260. http://dx.doi.org/10.5348/ijcri-2013-05-308-cr-5.

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36

Colombo, Fernando, Claus Cursiefen, Friedrich W. Neukam, and Leonard M. Holbach. "Orbital involvement in cherubism." Ophthalmology 108, no. 10 (2001): 1884–88. http://dx.doi.org/10.1016/s0161-6420(01)00757-6.

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37

Hernández-Alfaro, Federico, Jorge Arenaz Búa, Javier Mareque Bueno, and Consuelo Badía. "Orthognathic Surgery in Cherubism." Journal of Oral and Maxillofacial Surgery 69, no. 2 (2011): 541–45. http://dx.doi.org/10.1016/j.joms.2010.07.065.

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38

Cariati, Paolo, Fernando Monsalve Iglesias, José Fernández Solís, Alfredo Valencia Laseca, and Ildefonso Martinez Lara. "Cherubism. A case report." Reumatología Clínica 13, no. 6 (2017): 352–53. http://dx.doi.org/10.1016/j.reuma.2016.06.002.

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39

Cariati, Paolo, Fernando Monsalve Iglesias, José Fernández Solís, Alfredo Valencia Laseca, and Ildefonso Martinez Lara. "Cherubism. A case report." Reumatología Clínica (English Edition) 13, no. 6 (2017): 352–53. http://dx.doi.org/10.1016/j.reumae.2016.06.006.

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40

PIGATTI, FERNANDA MOMBRINI, MARCELA BAZANA MOREIRA DE SOUZA, FERNANDO SIMÕES MORANDO, ANDRÉ CAROLI ROCHA, and MARÍLIA TRIERVEILER MARTINS. "Cherubism: A Clinicopathological Correlation." Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology 120, no. 2 (2015): e71. http://dx.doi.org/10.1016/j.oooo.2015.02.311.

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41

Carroll, Andrew L., and Timothy J. Sullivan. "Orbital involvement in cherubism." Clinical and Experimental Ophthalmology 29, no. 1 (2001): 38–40. http://dx.doi.org/10.1046/j.1442-9071.2001.00363.x.

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42

Lacorzana, Javier, and CarlosGalvez Prieto-Moreno. "Cherubism with orbital involvement." Indian Journal of Ophthalmology 68, no. 11 (2020): 2534. http://dx.doi.org/10.4103/ijo.ijo_870_20.

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43

HAMAMOTO, Kazuhiko, Shosuke MORITA, Masahiro NAKAJIMA, Hideya HAENIWA, Hirotaka YAMAMOTO, and Kenji KAKUDO. "A case of cherubism." Japanese Journal of Oral & Maxillofacial Surgery 46, no. 2 (2000): 117–19. http://dx.doi.org/10.5794/jjoms.46.117.

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44

Lannon, Declan A., and Michael J. Earley. "Cherubism and its charlatans." British Journal of Plastic Surgery 54, no. 8 (2001): 708–11. http://dx.doi.org/10.1054/bjps.2001.3701.

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45

Papadaki, Maria E., Steven A. Lietman, Michael A. Levine, Bjorn R. Olsen, Leonard B. Kaban, and Ernst J. Reichenberger. "Cherubism: best clinical practice." Orphanet Journal of Rare Diseases 7, Suppl 1 (2012): S6. http://dx.doi.org/10.1186/1750-1172-7-s1-s6.

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46

Yoo, Sylvia H., Stacy L. Pineles, Reza Jarrahy, and Federico G. Velez. "Ophthalmic manifestations of cherubism." Journal of American Association for Pediatric Ophthalmology and Strabismus 19, no. 1 (2015): 70–72. http://dx.doi.org/10.1016/j.jaapos.2014.08.011.

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47

Koury, Mike E., John P. Stella, and Bruce N. Epker. "Vascular transformation in cherubism." Oral Surgery, Oral Medicine, Oral Pathology 76, no. 1 (1993): 20–27. http://dx.doi.org/10.1016/0030-4220(93)90287-e.

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48

Degala, Saikrishna, K. P. Mahesh, and Monalisha. "Cherubism: A Case Report." Journal of Maxillofacial and Oral Surgery 14, S1 (2013): 258–62. http://dx.doi.org/10.1007/s12663-013-0474-y.

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49

Bhattacharya, Surajit, and R. K. Mishra. "Fibrous dysplasia and cherubism." Indian Journal of Plastic Surgery 48, no. 03 (2015): 236–48. http://dx.doi.org/10.4103/0970-0358.173101.

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ABSTRACTFibrous dysplasia (FD) is a non-malignant fibro-osseous bony lesion in which the involved bone/bones gradually get converted into expanding cystic and fibrous tissue. The underlying defect in FD is post-natal mutation of GNAS1 gene, which leads to the proliferation and activation of undifferentiated mesenchymal cells arresting the bone development in woven phase and ultimately converting them into fibro-osseous cystic tissue. Cherubism is a hereditary form of fibrous dysplasia in which the causative factor is transmission of autosomal dominant SH3BP2 gene mutation. The disease may pres

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50

Fonseca, Luciana Cardoso, João Batista de Freitas, Pedro Hernane Maciel, and Marcelo Gusmão Paraiso Cavalcanti. "Temporal bone involvement in Cherubism: case report." Brazilian Dental Journal 15, no. 1 (2004): 75–78. http://dx.doi.org/10.1590/s0103-64402004000100014.

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Cherubism is a rare benign hereditary fibro-osseous disease involving the mandible and maxilla. We report a case of cherubism in a 10-year-old girl for which the panoramic radiograph was insufficient for diagnosis of the disease. Clinical, histological, and radiological findings were discussed. The CT was taken and it confirmed not only the involvement of the jaws but also of the temporal bone. This was not found in the conventional radiograph.

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