Tumeurs hamartomateuses et pluritissulaires

R.H. Khonsari1, J. Lepourry1, P. Corre1
1Service de chirurgie maxillofaciale et stomatologie, CHU de Nantes, CHU Hôtel-Dieu, 1, place Alexis-Ricordeau, 44000 Nantes, France

Tài liệu tham khảo

Wijn, 2007, Oral and maxillofacial manifestations of familial adenomatous polyposis, Oral Dis, 13, 360, 10.1111/j.1601-0825.2006.01293.x Harned, 1991, Extracolonic manifestations of the familial adenomatous polyposis, AJR Am J Roentgenol, 156, 481, 10.2214/ajr.156.3.1847274 Bulow, 1987, Incidence of associated diseases in familial polyposis coli, Semin Surg Oncol, 3, 84, 10.1002/ssu.2980030207 Evans, 1993, Complications of the naevoid basal cell carcinoma syndrome: results of a population based study, J Med Genet, 30, 460, 10.1136/jmg.30.6.460 Di Rocco, 2006, Sturge-Weber syndrome, Childs Nerv Syst, 22, 909, 10.1007/s00381-006-0143-2 Crawford, 1986, Osseous manifestations of neurofibromatosis in childhood, J Pediatr Orthop, 6, 72, 10.1097/01241398-198601000-00015 Korbmacher, 2005, Dentomaxillofacial imaging in Proteus syndrome, Dentomaxillofac Radiol, 34, 251, 10.1259/dmfr/22554007 Biesecker, 2006, The challenges of Proteus syndrome: diagnosis and management, Eur J Hum Genet, 14, 1151, 10.1038/sj.ejhg.5201638 Gorlin, 2001, Hennekam RCM. Syndromes of the head and neck, 428 Damm, 1999, Intraosseous fibrous lesions of the jaws: a manifestation of tuberous sclerosis, Oral Surg Oral Med Oral Pathol Oral Radiol Endod, 87, 334, 10.1016/S1079-2104(99)70219-2 Cassetty, 2004, Tuberous sclerosis complex (Bourneville disease), Dermatol Online J, 10, 17, 10.5070/D38Q09K4G3 Narayanan, 2003, Tuberous sclerosis complex: genetics to pathogenesis, Pediatr Neurol, 29, 404, 10.1016/j.pediatrneurol.2003.09.002 da Silveira, 2006, Partial facial hemihyperplasia with 9 years of evolution: case report and review of the literature, Oral Surg Oral Med Oral Pathol Oral Radiol Endod, 102, 505 Knudson, 2001, Two genetic hits (more or less) to cancer, Nat Rev Cancer, 1, 157, 10.1038/35101031 Blumenthal, 2008, PTEN hamartoma syndromes, Eur J Hum Genet, 16, 1289, 10.1038/ejhg.2008.162 Hamm, 1999, Cutaneous mosaicism of lethal mutations, Am J Med Genet, 85, 342, 10.1002/(SICI)1096-8628(19990806)85:4<342::AID-AJMG6>3.0.CO;2-8 Happle, 2007, Qu’est ce qu’un hamartome ? Et la confusion continue…, Ann Dermatol Venereol, 134, 75, 10.1016/S0151-9638(07)88998-8 Dubernard, 2008, Face transplantation, Lancet, 372, 603, 10.1016/S0140-6736(08)61252-0 Lantieri, 2008, Repair of the lower and middle parts of the face by composite tissue allotransplantation in a patient with massive plexiform neurofibroma: a 1-year follow-up study, Lancet, 372, 639, 10.1016/S0140-6736(08)61277-5 Khonsari, 2009, Partial facial hemihypertrophia with unusual soft tissue anomalies: long term follow-up, J Oral Maxillofac Surg, 67, 2310, 10.1016/j.joms.2009.03.029