Neurofibromatose tipo 1 e suas manifestações bucomaxilofaciais
Oral and maxillofacial manifestations of neurofibromatosis type 1
Cunha Filho, J.J.; Scortegagna, A.; Martins, F.; Schwengber, M.M.B.; Robinson, W.M.
Rev. odontol. UNESP, vol.37, n3, p.283-289, 2008
Resumo
A neurofibromatose é uma doença hereditária autossômica dominante que afeta, sobretudo, os tecidos moles. O objetivo deste estudo foi revisar aspectos clínicos e radiográficos bucomaxilofaciais da Neurofibromatose tipo 1 (NF1). Foi realizada uma busca por artigos publicados nas bases de dados Pubmed e Lilacs. Estudos com grande poder de gerar evidência não foram encontrados na literatura consultada. Estudos transversais sugeriram que manifestações bucomaxilofaciais da NF1 são mais freqüentes do que anteriormente imaginado. Os sinais clínicos mais relatados envolvem a presença de neurofibromas intrabucais, assimetrias faciais e alargamento das papilas fungiformes da língua. Radiograficamente, os estudos determinaram alargamentos do forame e canal mandibulares, displasias ósseas e neurofibromas intra-ósseos como alterações relacionadas à síndrome.
Palavras-chave
Doença de von Recklinghausen, doença hereditária, neurofibroma, NF1
Abstract
Neurofibromatosis is an autosomal dominant hereditary disease that affects mainly soft tissues. The aim of this study was to review clinical and radiological features of Neurofibromatosis type 1 (NF1) in oral and maxillofacial tissues. A search for scientific articles was performed in Pubmed and Lilacs databases. Studies with an evidence of high power were not found. Cross-sectional studies suggested that oral and maxillofacial manifestations of NF1 are more frequently than previously believed. The most related clinical signs are oral neurofibromas, facial asymmetry and enlarged fungiform papillae of the tongue. Radiographically, studies found enlarged mandibular foramem and canal, osseous dysplasia and intraosseous neurofibromas as manifestations related to NF1.
Keywords
Von Recklinghausen disease, hereditary disease, neurofibroma, NF1
Referências
1. Szudek J, Birch P, Riccardi VM, Evans DG, Friedman JM. Associations of clinical features in neurofibromatosis 1 (NF1). Genet Epidemiol. 2000;19:429-39.
2. Robinson W, Borges-Osório. Genética para odontologia. Porto Alegre: Artmed; 2006.
3. Friedrich RE, Giese M, Schmelzle R, Mautner VF, Scheuer HA. Jaw malformations plus displacement and numerical aberrations of teeth in neurofibromatosis type 1: a descriptive analysis of 48 patients based on panoramic radiographs and oral findings. J Craniomaxillofac Surg. 2003;31:1-9.
4. Ruggieri M, Huson SM. The clinical and diagnostic implications of mosaicism in the neurofibromatoses. Neurology. 2001;56:1433-43.
5. Shapiro SD, Abramovitch K, Van Dis ML, Skoczylas LJ, Langlais RP, Jorgenson RJ, et al. Neurofibromatosis: oral and radiographic manifestations. Oral Surg Oral Med Oral Pathol. 1984;58:493-8.
6. D’Ambrosio JA, Langlais RP, Young RS. Jaw and skull changes in neurofibromatosis. Oral Surg Oral Med Oral Pathol. 1988;66:391-6.
7. Visnapuu V, Peltonen S, Ellila T, Kerosuo E, Vaananen K, Happonen RP, et al. Periapical cemental dysplasia is common in women with NF1. Eur J Med Genet. 2007;50:274-80.
8. Kaplan I, Calderon S, Kaffe I. Radiological findings in jaws and skull of neurofibromatosis type 1 patients. Dentomaxillofac Radiol. 1994;23:216-20.
9. Sigillo R, Rivera H, Nikitakis NG, Sauk JJ. Neurofibromatosis type 1: a clinicopathological study of the orofacial manifestations in 6 pediatric patients. Pediatr Dent. 2002;24:575-80.
10. Lee L, Yan YH, Pharoah MJ. Radiographic features of the mandible in neurofibromatosis: a report of 10 cases and review of the literature. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 1996;81:361-7.
11. Tucker T, Birch P, Savoy DM, Friedman JM. Increased dental caries in people with neurofibromatosis 1. Clin Genet. 2007;72:524-7.
12. Bongiorno MR, Pistone G, Arico M. Manifestations of the tongue in neurofibromatosis type 1. Oral Dis. 2006;12:125-9.
13. De Lange J, Van den Akker HP. Clinical and radiological features of central giant-cell lesions of the jaw. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2005;99:464-70.
14. Marocchio LS, Oliveira DT, Pereira MC, Soares CT, Fleury RN. Sporadic and multiple neurofibromas in the head and neck region: a retrospective study of 33 years. Clin Oral Investig. 2007;11:165-9.
15. National Institutes of Health Consensus Development Conference Statement: neurofibromatosis. Bethesda, Md, USA, July 13-15, 1987. Neurofibromatosis. 1988;1:172-8.
16. Gutmann DH, Aylsworth A, Carey JC, Korf B, Marks J, Pyeritz RE, et al. The diagnostic evaluation and multidisciplinary management of neurofibromatosis 1 and neurofibromatosis 2. J Am Med Assoc. 1997;278:51-7.
17. Neville BW, Damn DD, Allen CM, Bouquot JE. Soft tissue tumors. Oral and maxillofacial pathology. Philadelphia: WB Saunders; 2002.
18. Preston FW, Walsh WS, Clarke TH. Cutaneous neurofibromatosis (Von Recklinghausen’s disease); clinical manifestation and incidence of sarcoma in sixty-one male patients. AMA Arch Surg. 1952;64:813-27.
19. Powell CA, Stanley CM, Bannister SR, McDonnell HT, Moritz AJ, Deas DE. Palatal neurofibroma associated with localized periodontitis. J Periodontol. 2006;77:310-5.
20. Bekisz O, Darimont F, Rompen EH. Diffuse but unilateral gingival enlargement associated with von Recklinghausen neurofibromatosis: a case report. J Clin Periodontol. 2000;27:361-5.
21. Becelli R, Renzi G, Cerulli G, Saltarel A, Perugini M. Von Recklinghausen neurofibromatosis with palatal localization. Diagnostic and surgical problems in two clinical cases. Minerva Stomatol. 2002;51:391-7.
22. Edwards PC, Fantasia JE, Saini T, Rosenberg TJ, Sachs SA, Ruggiero S. Clinically aggressive central giant cell granulomas in two patients with neurofibromatosis 1. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2006;102:765-72.
23. Ruggieri M, Pavone V, Polizzi A, Albanese S, Magro G, Merino M, et al. Unusual form of recurrent giant cell granuloma of the mandible and lower extremities in a patient with neurofibromatosis type 1. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 1999;87:67-72.
24. Ardekian L, Manor R, Peled M, Laufer D. Bilateral central giant cell granulomas in a patient with neurofibromatosis: report of a case and review of the literature. J Oral Maxillofac Surg. 1999;57:869-72.
25. Zoller ME, Rembeck B, Oden A, Samuelsson M, Angervall L. Malignant and benign tumors in patients with neurofibromatosis type 1 in a defined Swedish population. Cancer. 1997;79:2125-31.
26. Neville BW, Hann J, Narang R, Garen P. Oral neurofibrosarcoma associated with neurofibromatosis type I. Oral Surg Oral Med Oral Pathol. 1991;72:456-61.
27. Allen CM, Miloro M. Gingival lesion of recent onset in a patient with neurofibromatosis. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 1997;84:595-7.
28. Muraki Y, Tateishi A, Tominaga K, Fukuda J, Haneji T, Iwata Y. Malignant peripheral nerve sheath tumour in the maxilla associated with von Recklinghausen’s disease. Oral Dis. 1999;5:250-2.
29. Antoniades K, Giannouli T, Kaisaridou D. Merkel cell carcinoma in a patient with Recklinghausen neurofibromatosis. Int J Oral Maxillofac Surg. 1998;27:213-4.
30. Susin C, Rösing CK. Seleção dos melhores métodos para a questão em estudo. In: Susin C, Rösing CK. Praticando odontologia baseada em evidências. Canoas: Editora da ULBRA; 1999. p. 33 - 57.
31. Gorlin RJ, Goldman HM. Patologia oral. 6ª ed. Espanha: Salvat; 1973.
32. Garcia de Marcos JA, Dean Ferrer A, Alamillos Granados F, Ruiz Masera JJ, Garcia de Marcos MJ, Vidal Jimenez A, et al. Gingival neurofibroma in a neurofibromatosis type 1 patient. Med Oral Patol Oral Cir Bucal. 2007;12:E287-91.
33. Cunha KS, Barboza EP, Dias EP, Oliveira FM. Neurofibromatosis type I with periodontal manifestation. A case report and literature review. Br Dent J. 2004;196:457-60.
34. Tsiklakis K, Nikopoulou-Karayianni A. Multiple neurofibromatosis associated with mandibular growth and facial asymmetry. Ann Dent. 1990;49(1):14-7.
35. Cohen MM, Jr. Perspectives on craniofacial asymmetry. VI. The hamartoses. Int J Oral Maxillofac Surg. 1995;24:195-200.