A dental approach to Proteus Syndrome: a case report

Authors

DOI:

https://doi.org/10.33448/rsd-v11i9.32078

Keywords:

Congenital malformations; Craniofacial abnormalities; Hamartomatous syndrome; Proteus syndrome.

Abstract

Proteus syndrome (SP; OMIM #176920) is a rare complex disorder, characterized by the asymmetric postnatal growth of different parts of the body which tends to progress throughout life. Its prevalence is estimated at 1 per 1,000,000 live births. The clinical features are: partial gigantism of extremities, plantar hyperplasia, macrocephaly, cranial hyperostosis and asymmetry of the limbs due to the growth of long bones and soft tissues. Some of those affected may have intellectual impairment. Diagnosis is based on clinical criteria, imaging and genetic exams. The mainstay of treatment is early diagnosis of the disease and medication for symptoms presenting throughout life to improve quality of life. This case report presents a female patient, from 4½ years of age to the present, with asymmetric growth of the face and upper and lower limbs, undergoing dental follow-up at the Dental Service of a Specialist Center for Rehabilitation and Readaptation in Goiânia, Brazil. She presents delay in neuropsychomotor development, pronounced osteopenia, does not speak and is dependent in terms of activities of daily living. The eruption of deciduous teeth began at 4 months and permanent dentition at 4 years of age. During the current clinical examination of the child at 12 years and 2 months we found severe enamel hypoplasia in the teeth on the right side, mandibular prognathism, maxillary atresia, ogival palate, and anterior crossbite. The treatment plan included prevention and maintenance of oral health, monitoring of enamel hypoplasia, rhizolysis of the deciduous dentition and of eruption of permanent dentition, and restoration and extraction of teeth which were causing traumatic lesions on soft tissues. The parents' concerns were the malformations in dental enamel and traumatic lesions in the mucous membranes caused by badly positioned teeth. The interventions performed were composite resin restorations, tooth extractions, oral hygiene guidance and topical application of fluoride. Orthodontic treatment was contraindicated due to the severity of the disease. The dental approach in severe cases of PS must be individualized, with emphasis on oral hygiene and the removal of traumatic factors which damage soft tissues and cause pain. Dental surgeons must be prepared for individualized management.

References

Becktor, K., Becktor, J., Karnes, P., & Keller, E. (2002). Craniofacial and Dental Manifestations of Proteus Syndrome: A Case Report. The Cleft Palate-Craniofacial Journal, 39(2), 233-45.

Biesecker LG, Sapp JC (2019). Proteus Syndrome. National Library of Medicine - Gene Reviews, 1-15.

Biesecker, L. G., Happle, R., Mulliken, J. B., Weksberg, R., Graham, J. M., Viljoen, D. L., & Cohen, M. M. (1999). Proteus syndrome: diagnostic criteria, differential diagnosis, and patient evaluation. American journal of medical genetics, 84(5), 389-95.

Biesecker, L. (2006). The challenges of Proteus syndrome: diagnosis and management. European Journal of Human Genetics, 14(11), 1151-7.

Biesecker, L. G., & Sapp, J. C. (2012). Proteus Syndrome. In M. P. Adam (Eds.) et. al., GeneReviews®. University of Washington, Seattle.

Brockmann, K., Happle, R., Oeffner, F., & König, A. (2008). Monozygotic twins discordant for Proteus syndrome. American Journal of Medical Genetics Part A, 146A(16), 2122-5.

Canabarro, A., Galheigo, T.M., Galheigo de Oliveira e Silva, D., & Tinoco, E.M. (2008). Periodontal findings and other oral manifestations in Proteus syndrome: a case report. Quintessence international (Berlin, Germany : 1985), 39(4), 307-11.

Cohen, M.M. (2014). Proteus syndrome review: molecular, clinical, and pathologic features. Clinical Genetics, 85(2), 111-9.

Cohen MM Jr, Hayden PW. (1979). A newly recognised hamartomatous syndrome. In O'Donnell JJ, Hall BD, eds. Penetrance and variability in malformation syndromes. The National Foundation—March of Dimes. BD: OAS XV (5B), 291–6.

Cohen, M. M. (2001). Causes of premature death in Proteus syndrome. American Journal of Medical Genetics, 101(1), 1-3.

Cohen, M. M. (2005). Proteus syndrome: An update. American Journal of Medical Genetics Part C: Seminars in Medical Genetics, 137C(1), 38-52.

Cohen, M. M. (1993). Proteus syndrome: Clinical evidence for somatic mosaicism and selective review. American Journal of Medical Genetics, 47(5), 645-52.

Estrela, C. (2018). Metodologia científica: ciência, ensino, pesquisa. 3.ed. Porto Alegre: Artes Médicas.

Friedrich, R. E. (2021). Phenotype and Surgical Treatment in a Case of Proteus Syndrome With Craniofacial and Oral Findings. In Vivo, 35(3), 1583-94.

Jamis-Dow, C. A., Turner, J., Biesecker, L. G., & Choyke, P. L. (2004). Radiologic Manifestations of Proteus Syndrome. RadioGraphics, 24(4), 1051-68.

Kaiser, R., Rothenfluh, E., Rothenfluh, D., Behrbalk, E., Perez Romera, A. B., Stokes, O. M., & Mehdian, H. (2015). Surgical correction of kyphotic deformity in a patient with Proteus syndrome. The Spine Journal, 15(7), e5-e12.

Keppler-Noreuil, K. M., Sapp, J. C., Lindhurst, M. J., Darling, T. N., Burton-Akright, J., Bagheri, M., . . . & Biesecker, L. G. (2019). Pharmacodynamic Study of Miransertib in Individuals with Proteus Syndrome. The American Journal of Human Genetics, 104(3), 484-91.

Korbmacher, H., Tietke, M., Rother, U., & Kahl-Nieke, B. (2005). Dentomaxillofacial imaging in Proteus syndrome. Dentomaxillofacial Radiology, 34(4), 251-5.

Lindhurst, M. J., Brinster, L. R., Kondolf, H. C., Shwetar, J. J., Yourick, M. R., Shiferaw, H., . . . & Biesecker, L. G. (2019). A mouse model of Proteus syndrome. Human Molecular Genetics, 28(17), 2920-36

Lindhurst, M. J., Sapp, J. C., Teer, J. K., Johnston, J. J., Finn, E. M., Peters, K., . . . & Biesecker, L. G. (2011). A Mosaic Activating Mutation inAKT1 Associated with the Proteus Syndrome. New England Journal of Medicine, 365(7), 611-9

Lougaris, V., Salpietro, V., Cutrupi, M., Baronio, M., Moratto, D., Pizzino, M.R., ... & Plebani, A. (2016). Proteus syndrome: evaluation of the immunological profile. Orphanet Journal of Rare Diseases, 11(1), 1-5.

Mason, C., & Roberts, G. (2009). Unusual distribution of enamel hypoplasia in an 11-year-old child with Proteus syndrome. International Journal of Paediatric Dentistry, 5(2), 103-7.

Munhoz, L., Arita, E. S., Nishimura, D. A., & Watanabe, P. C. A. (2021). Maxillofacial manifestations of Proteus syndrome: a systematic review with a case report. Oral Radiology, 37(1), 2-12.

Panteliadis, C. P., Friedrich, R. E. (2022). Proteus Syndrome. In: Panteliadis, C. P., Benjamin, R., Hagel, C. (eds) Neurocutaneous Disorders. Springer, Cham.

Sapp, J. C., Buser, A., Burton‐Akright, J., Keppler‐Noreuil, K. M., & Biesecker, L. G. (2019). A dyadic genotype–phenotype approach to diagnostic criteria for Proteus syndrome. American Journal of Medical Genetics Part C: Seminars in Medical Genetics, 181(4), 565-70.

Sapp, J. C., Hu, L., Zhao, J., Gruber, A., Schwartz, B., Ferrari, D., & Biesecker, L. G. (2017). Quantifying survival in patients with Proteus syndrome. Genetics in Medicine, 19(12), 1376-9.

Satter, E. (2007). Proteus syndrome: 2 case reports and a review of the literature. Cutis, 80(4), 297-302

Tibbles, J. A., & Cohen, M. M. (1986). The Proteus syndrome: the Elephant Man diagnosed.. BMJ, 293(6548), 683-5.

Tosi, L. L., Sapp, J. C., Allen, E. S., O'Keefe, R. J., &Biesecker, L. G. (2011). Assessment and management of the orthopedic and other complications of Proteus Syndrome. Journal of Children`s Orthopaedics, 5(5), 319-327

Turner, J. T., Cohen, M. M., & Biesecker, L. G. (2004). Reassessment of the Proteus syndrome literature: application of diagnostic criteria to published cases. American journal of medical genetics. Part A, 130A(2), 111-22.

Twede, J. V., Turner, J. T., Biesecker, L. G., & Darling, T. N. (2005). Evolution of skin lesions in Proteus syndrome. Journal of the American Academy of Dermatology, 52(5), 834-8.

Valéra, M., Vaysse, F., Bieth, E., Longy, M., Cances, C., & Bailleul-Forestier, I. (2015). Proteus syndrome: Report of a case with AKT1 mutation in a dental cyst. European Journal of Medical Genetics, 58(5), 300-4.

Wiedemann, H., Burgio, G. R., Aldenhoff, P., Kunze, J., Kaufmann, H. J., & Schirg, E. (1983). The proteus syndrome. European Journal of Pediatrics, 140(1), 5-12.

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Published

16/07/2022

How to Cite

ROCHA, V. I. P.; GOMES, B. Y. .; CAUHI, L. de P. .; BENICIO, R. O. A. .; HADDAD, A. S. . A dental approach to Proteus Syndrome: a case report. Research, Society and Development, [S. l.], v. 11, n. 9, p. e47811932078, 2022. DOI: 10.33448/rsd-v11i9.32078. Disponível em: https://rsdjournal.org/index.php/rsd/article/view/32078. Acesso em: 24 nov. 2024.

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Health Sciences