2021, Número 3
<< Anterior
Rev Mex Cir Bucal Maxilofac 2021; 17 (3)
Glosectomía parcial con técnica de resección en cuña estelar y colgajo de rotación anterior para el tratamiento de la macroglosia por linfangioma
Gómez HKA, Castilla CH, Ruíz VY
Idioma: Ingles.
Referencias bibliográficas: 37
Paginas: 156-164
Archivo PDF: 385.88 Kb.
RESUMEN
La macroglosia es una afección caracterizada por el aumento del tamaño de la lengua causado por malformaciones congénitas como linfangiomas, corioestomas, hamartomas, o malformaciones adquiridas como neoplasias benignas o malignas. En la mayoría de los casos, el tratamiento es quirúrgico y puede ser conservador cuando la vía aérea no está comprometida. En este trabajo presentamos el caso de un paciente varón de dos años con diagnóstico de macroglosia por linfangioma. El protocolo de tratamiento consistió en una glosectomía parcial mediante la técnica de resección en cuña estelar y colgajo de rotación anterior, así como terapia del habla tras la fase quirúrgica. Tras un año de seguimiento, se observó la persistencia de la lesión, lo que mereció una segunda intervención quirúrgica en la que se consiguió una dimensión lingual de parámetros normales, preservando la armonía estética y funcional sin causar alteraciones neurosensoriales ni gustativas.
REFERENCIAS (EN ESTE ARTÍCULO)
Ring ME. The treatment of macroglossia before the 20th century. Am J Otolaryngol - Head Neck Med Surg. 1999; 20: 28-36. Available in: https://doi.org/10.1016/S0196-0709(99)90047-9
Anichini C, Lotti F, Cencini A, Caruso G, Stortini G, Spinelli M. Macroglossia as a cause of atypical swallowing: comparison of evaluation and logopedic treatment between Beckwith-Wiedemann and down patients. J Siena Acad Sci. 2013; 5: 75. Available in: https://doi.org/10.4081/jsas.2013.75
Simmonds JC, Patel AK, Mildenhall NR, Mader NS, Scott AR. Neonatal macroglossia: demographics, cost of care, and associated comorbidities. Cleft Palate Craniofac J. 2018; 55 (8): 1122-1129. Available in: https://doi.org/10.1177/1055665618760898
Balaji S. Reduction glossectomy for large tongues. Ann Maxillofac Surg. 2013; 3 (2): 167-172. Available in: https://doi.org/10.4103/2231-0746.119230
Pau M, Reinbacher KE, Feichtinger M, Karcher H. Surgical treatment of macroglossia caused by systemic primary amyloidosis. Int J Oral Maxillofac Surg. 2013; 42 (2): 294-297. Available in: https://doi.org/10.1016/j.ijom.2012.05.015
Galaz-Montoya CI, García-Delgado C, Cervantes-Peredo A, García-Morales L, Morán-Barroso VF. Perfil clínico de una cohorte de pacientes con síndrome de Silver-Russell atendidos en el Hospital Infantil de México Federico Gómez de 1998 a 2012. Bol Med Hosp Infant Mex. 2014; 71 (4): 218-226. Available in: https://doi.org/10.1016/j.bmhimx.2014.08.001
Kovach TA, Kang DR, Triplett RG. Massive macroglossia secondary to angioedema: a review and presentation of a case. J Oral Maxillofac Surg. 2015; 73: 905-917. Available in: https://doi.org/10.1016/j.joms.2014.12.029
Melville JC, Menegotto KD, Woernley TC, Maida BD, Alava I. Unusual case of a massive macroglossia secondary to myxedema: a case report and literature review. J Oral Maxillofac Surg. 2018; 76: 119-127. Available in: https://doi.org/10.1016/j.joms.2017.06.033
Bouaoud J, Joly A, Picard A, Thierry B, Arnaud E, James S et al. Severe macroglossia after posterior fossa and craniofacial surgery in children. Int J Oral Maxillofac Surg. 2018; 47: 428-436. Available in: https://doi.org/10.1016/j.ijom.2017.12.003
Gardon MA, Andre CV, Ernenwein D, Teissier N, Bennaceur S. New surgical method of tongue reduction for macroglossia: technical note. Oral Surg Oral Med Oral Pathol Oral Radiol. 2019; 127: e1-7. Available in: https://doi.org/10.1016/j.oooo.2018.06.013
Heggie AAC, Vujcich NJ, Portnof JE, Morgan AT. Tongue reduction for macroglossia in Beckwith Wiedemann syndrome: review and application of new technique. Int J Oral Maxillofac Surg. 2013; 42: 185-191. Available in: https://doi.org/10.1016/j.ijom.2012.09.003
Toranzo-Fernández JM, Duarte-Hernández S, Rodríguez-Pérez A. Síndrome de Beckwith-Wiedemann: reporte de tres casos. Revista ADM. 2001; 58 (5): 170-172.
Wolford LM, Cottrell DA. Diagnosis of macroglossia and indications for reduction glossectomy. Am J Orthod Dentofacial Orthop. 1996; 110 (2): 170-177.
Canseco HC, Villa BU. Hiperplasia condilar bilateral manejo quirúrgico. Reporte de caso. Rev Mex Cir Bucal Maxilofac. 2016; 12: 10-20.
Prada CE, Zarate YA, Hopkin RJ. Genetic causes of macroglossia: diagnostic approach. Pediatrics. 2012; 129. Available in: https://doi.org/10.1542/peds.2011-1732
Greene AK, Perlyn CA, Alomari AI. Management of lymphatic malformations. Clin Plast Surg. 2011; 38: 75-82. Available in: https://doi.org/10.1016/j.cps.2010.08.006
Kolokythas A. Vascular malformations and theirtreatment in the growing patient. Oral Maxillofac Surg Clin North Am. 2016; 28: 91-104. Available in: https://doi.org/10.1016/j.coms.2015.07.006
Bonet-Coloma C, Minguez-Martínez I, Aloy-Prósper A, Rubio-Serrano M, Peñarrocha-Diago MA, Peñarrocha-Diago M. Clinical characteristics, treatment, and evolution in 14 cases of pediatric orofacial lymphangioma. J Oral Maxillofac Surg. 2011; 69: e96-99. Available in: https://doi.org/10.1016/j.joms.2010.07.029
Bouchard C, Peacock ZS, Troulis MJ. Pediatric vascular tumors of the head and neck. Oral Maxillofac Surg Clin North Am. 2016; 28: 105-113. https://doi.org/10.1016/j.coms.2015.07.010
Colletti G, Valassina D, Bertossi D, Melchiorre F, Vercellio G, Brusati R. Contemporary management of vascular malformations. J Oral Maxillofac Surg. 2014; 72: 510-528. Available in: https://doi.org/10.1016/j.joms.2013.08.008
Webb DE, McDermott J, Grover D. Vascular anomalies of the neck. Atlas Oral Maxillofac Surg Clin North Am. 2015; 23: 63-78. Available in: https://doi.org/10.1016/j.cxom.2014.11.001
Neville BW, Damm DD, Allen CM CA. Oral and maxillofacial pathology. 4°. Canada: Elsevier; 2016.
Noia G, Maltese PE, Zampino G, D'Errico M, Cammalleri V, Convertini P et al. Cystic hygroma: a preliminary genetic study and a short review from the literature. Lymphat Res Biol. 2019; 17: 30-39. Available in: https://doi.org/10.1089/lrb.2017.0084
Abramowicz S, Padwa BL. Vascular anomalies in children. Oral Maxillofac Surg Clin North Am. 2012; 24: 443-455. Available in: https://doi.org/10.1016/j.coms.2012.05.001
Bloom DC, Perkins JA, Manning SC. Management of lymphatic malformations and macroglossia: results of a national treatment survey. Int J Pediatr Otorhinolaryngol. 2009; 73: 1114-1118. Available in: https://doi.org/10.1016/j.ijporl.2009.04.016
Perkins JA, Manning SC, Tempero RM, Cunningham MJ, Edmonds JLJ, Hoffer FA et al. Lymphatic malformations: review of current treatment. Otolaryngol Neck Surg Off J Am Acad Otolaryngol Neck Surg. 2010; 142: 795-803, 803.e1. Available in: https://doi.org/10.1016/j.otohns.2010.02.026
Lauretano AM, Li KK, Caradonna DS, Khosta RK, Fried MP. Anatomic location of the tongue base neurovascular bundle. Laryngoscope. 1997; 107: 1057-109. Available in: https://doi.org/10.1097/00005537-199708000-00010
Limbrock GJ, Castillo-Morales R, Hoyer H, Stover B, Onufer CN. The Castillo-Morales approachto orofacial pathology in Down syndrome. Int Assoc Orofac Myol. 1993; 19: 30-37.
Jiao-ling L, Hai-ying W, Wei Z, Jin-rong L, Kun-shan C, Qian F. Treatment and prognosis of fetal lymphangioma. Eur J Obstet Gynecol Reprod Biol. 2018; 231: 274-279. Available in: https://doi.org/10.1016/j.ejogrb.2018.10.031
Choi JW, Kim HJ, Park HS, Kwon TG. Congenital macroglossia treated by 2-stage partial glossectomy. J Craniofac Surg. 2013; 24: 554-556. Available in: https://doi.org/10.1097/SCS.0b013e31826cff10
Kadouch DJM, Maas SM, Dubois L, Van Der Horst CMAM. Surgical treatment of macroglossia in patients with Beckwith-Wiedemann syndrome: a 20-year experience and review of the literature. Int J Oral Maxillofac Surg. 2012; 41: 300-308. Available in: https://doi.org/10.1016/j.ijom.2011.10.021
Naujokat H, Moller B, Terheyden H, Birkenfeld F, Caliebe D, Krause MF et al. Tongue reduction in Beckwith-Wiedemann syndrome: outcome and treatment algorithm. Int J Oral Maxillofac Surg. 2019; 48: 9-16. Available in: https://doi.org/10.1016/j.ijom.2018.07.008
Somers EH, Samson TD. Keyhole tongue reduction. Oper Tech Otolaryngol-Head Neck Surg. 2015; 26: 127-130. Available in: https://doi.org/10.1016/j.otot.2015.06.005
Maas SM,Kadouch DJ, Masselink ACCM, Van Der Horst CMAM. Taste and speech following surgical tongue reduction in children with Beckwith-Wiedemann syndrome. J Cranio-Maxillofacial Surg. 2016; 44: 659-663. Available in: https://doi.org/10.1016/j.jcms.2016.02.010
Kacker A, Honrado C, Martin D, Ward R. Tongue reduction in Beckwith-Weidemann syndrome. Int J Pediatr Otorhinolaryngol. 2000; 53: 1-7. Available in: https://doi.org/10.1016/S0165-5876(00)00280-9
Linden RW. Taste. Br Dent J. 1993; 175: 243-253. Available in: https://doi.org/10.1038/sj.bdj.4808291
Okazaki T, Iwatani S, Yanai T, Kobayashi H, Kato Y, Marusasa T et al. Treatment of lymphangioma in children: our experience of 128 cases. J Pediatr Surg. 2007; 42: 386-389. Available in: https://doi.org/10.1016/j.jpedsurg.2006.10.012