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Hemifacial Microsomia: A Case Report and Overview

Year 2014, Volume: 39 Issue: 3, 625 - 635, 22.07.2014
https://doi.org/10.17826/cutf.74086

Abstract

Hemifacial Microsomia is a developmental craniofacial anomaly typically displaying reduced growth and development of half of the face as a result of abnormal development of first and second branchial arches. The patients with Hemifacial Microsomia usually exhibit unilateral involvement of the face but occasionally might involve both the sides. Cases which show vertebral anomalies and epibulbar dermoids have been considered to form a separate category within this condition . The condition is now known to be extremely complex and heterogenous. Here we present a case of Hemifacial Microsomia with its characteristic clinical and radiographic features that will help us in diagnosing and differentiating this rare entity from other closely related syndromes

References

  • Gorlin RJ, Jue KL, Jacobsen U, et al. Oculoauriculovertebral dysplasia. J Pediatr. 1963;63:991-9.
  • Gorlin RJ, Cohen MM, Levin LS. Syndromes of the head and neck. 3 rd edition, McGrawHill.Inc., Oxford university Press.,1990;641-55.
  • Jongbloet PH. Goldenhar syndrome and overlapping dysplasias. J Med Genet. 1987;24:616-20.
  • Munjal D. Hemifacial microsomia: A case report and review of literature. J Indian Assoc Oral Maxillofac Radiol. 2006;18:64-9.
  • Monahan R, Seder K, Patel P, Alder M, Grud S, O’Gara M. Hemifacial microsomia: Etiology, diagnosis and treatment. Am Dent Assoc. 2001;132:1402-8.
  • Raymond WS, Angelisa MP, Samson L, Michael LC. Hemifacial microsmia in pediatric patients: Asymmetric abnormal development of the first and second branchial arche. AJR. 2002;178:1523-30.
  • Kalsotra P, Chowdhary A, Bhagat DR, Parihar SS, Prabhakar R. Craniofacial microsomia. J K Sci. 2006;8:168-70.
  • Wang RR, Andres CJ. Hemifacial microsomia and treatment options for auricular replacement: A review of literature. J. Prosthet Dent. 1999;82:197-204
  • Rollinck BR, Kaye CI. Hemifacial microsomia and variants:Pedigree data. Am J Med Genet. 1983;15:233-53.
  • Poswillo DE. Etiology and pathogenesis of first and second branchial arch defects: the contribution of animal studies. In: Symposium on Diagnosis and Treatment of Craniofacial Anomalies. Eds.: McCarthy JG. Wood-Smith D. New York University. 1976;20.
  • Poswillo D. The pathogenesis of the first and second branchial arch syndrome. Oral Surg. Oral Med. Oral Pathol. 1973;35:302–28.
  • Johnston M.C, Bronsky P.T. Animal models for human craniofacial malformations. J Craniofac Genet Dev Biol. 1991;11:277–91.
  • Thomas J.T. Frias J.L. The heart in selected congenital malformations: a lesson in pathogenetic relationships. Ann Clin Lab Sci. 1987;17:207–10.
  • Chaudhari SY. Craniofacial microsomia: A rare case report. J Oral Maxillofac Radiol. 2013;1:70-4.
  • Carvalho GJ, Song CS, Vargervik K, Lalwani AK. Auditory and facial nerve dysfunction in patients with hemifacial microsomia. Arch Otolaryngol Head Neck Surg. 1999;125:209-12.
  • Romsee MC, Verdonck A, Schoenaers J, Carels C. Treatment of hemifacial microsomia in a growing child: the importance of co-operation between the orthodontist and the maxillofacial surgeon. J. Orthod. 2004;31:190–200.
  • Vento AR, LaBrie RA, Mulliken JB. The O.M.E.N.S. classification of hemifacial microsomia. Cleft Palate Craniofac J. 1991;28:68-77.
  • Rajendran R, Sivapathasundaram B. Shafer’s textbook of oral pathology. 5th ed, Elsevier, New Delhi. 2006;986:1189-90.
  • McCarthy JG. Craniofacial microsomia. Joseph Grabb and smith’s plastic surgery sixth edition by Charles H. Thorne. Chapter 2007;26:248-55.
  • Kapur RA, Kapur RB, Sheikh SC, Jindal SD, Kulkarni SE. Hemifacial microsomia: A case report. J Indian Soc Pedod Prevent Dent. 2008;34-40.

Hemifasyal Mikrozomi: Olgu Sunumu ve Genel Bakış

Year 2014, Volume: 39 Issue: 3, 625 - 635, 22.07.2014
https://doi.org/10.17826/cutf.74086

Abstract

Hemifasyal mikrozomi tipik olarak birinci ve ikinci brankial arkların anormal gelişimi sonucu yüzün yarısında eksik büyüme ve gelişme gösteren gelişimsel kraniofasiyal bir anomalidir. Hemifasyal mikrozomi genellikle hastalarda yüzün tek bir tarafında ortaya çıkmaktayken nadiren her iki tarafıda içerdiği vakalarda mevcuttur. Vertebral anomali ve epibulbar dermoid gösteren vakalar ise bu durumlar içerisinde farklı bir kategoride değerlendirilir. Bu yapı oldukça kompleks ve heterojenite gösteren bir durum olarak bilinir. Burada; bilinen yakın ilişkili sendromlardan farklı olarak, bu nadir durumumun ayırt edilmesi ve teşhisi için bize yardımcı olacak karakteristik klinik ve radyografik özellikli Hemifasyal mikrozomili bir vaka sunulmaktadır.

References

  • Gorlin RJ, Jue KL, Jacobsen U, et al. Oculoauriculovertebral dysplasia. J Pediatr. 1963;63:991-9.
  • Gorlin RJ, Cohen MM, Levin LS. Syndromes of the head and neck. 3 rd edition, McGrawHill.Inc., Oxford university Press.,1990;641-55.
  • Jongbloet PH. Goldenhar syndrome and overlapping dysplasias. J Med Genet. 1987;24:616-20.
  • Munjal D. Hemifacial microsomia: A case report and review of literature. J Indian Assoc Oral Maxillofac Radiol. 2006;18:64-9.
  • Monahan R, Seder K, Patel P, Alder M, Grud S, O’Gara M. Hemifacial microsomia: Etiology, diagnosis and treatment. Am Dent Assoc. 2001;132:1402-8.
  • Raymond WS, Angelisa MP, Samson L, Michael LC. Hemifacial microsmia in pediatric patients: Asymmetric abnormal development of the first and second branchial arche. AJR. 2002;178:1523-30.
  • Kalsotra P, Chowdhary A, Bhagat DR, Parihar SS, Prabhakar R. Craniofacial microsomia. J K Sci. 2006;8:168-70.
  • Wang RR, Andres CJ. Hemifacial microsomia and treatment options for auricular replacement: A review of literature. J. Prosthet Dent. 1999;82:197-204
  • Rollinck BR, Kaye CI. Hemifacial microsomia and variants:Pedigree data. Am J Med Genet. 1983;15:233-53.
  • Poswillo DE. Etiology and pathogenesis of first and second branchial arch defects: the contribution of animal studies. In: Symposium on Diagnosis and Treatment of Craniofacial Anomalies. Eds.: McCarthy JG. Wood-Smith D. New York University. 1976;20.
  • Poswillo D. The pathogenesis of the first and second branchial arch syndrome. Oral Surg. Oral Med. Oral Pathol. 1973;35:302–28.
  • Johnston M.C, Bronsky P.T. Animal models for human craniofacial malformations. J Craniofac Genet Dev Biol. 1991;11:277–91.
  • Thomas J.T. Frias J.L. The heart in selected congenital malformations: a lesson in pathogenetic relationships. Ann Clin Lab Sci. 1987;17:207–10.
  • Chaudhari SY. Craniofacial microsomia: A rare case report. J Oral Maxillofac Radiol. 2013;1:70-4.
  • Carvalho GJ, Song CS, Vargervik K, Lalwani AK. Auditory and facial nerve dysfunction in patients with hemifacial microsomia. Arch Otolaryngol Head Neck Surg. 1999;125:209-12.
  • Romsee MC, Verdonck A, Schoenaers J, Carels C. Treatment of hemifacial microsomia in a growing child: the importance of co-operation between the orthodontist and the maxillofacial surgeon. J. Orthod. 2004;31:190–200.
  • Vento AR, LaBrie RA, Mulliken JB. The O.M.E.N.S. classification of hemifacial microsomia. Cleft Palate Craniofac J. 1991;28:68-77.
  • Rajendran R, Sivapathasundaram B. Shafer’s textbook of oral pathology. 5th ed, Elsevier, New Delhi. 2006;986:1189-90.
  • McCarthy JG. Craniofacial microsomia. Joseph Grabb and smith’s plastic surgery sixth edition by Charles H. Thorne. Chapter 2007;26:248-55.
  • Kapur RA, Kapur RB, Sheikh SC, Jindal SD, Kulkarni SE. Hemifacial microsomia: A case report. J Indian Soc Pedod Prevent Dent. 2008;34-40.
There are 20 citations in total.

Details

Primary Language Turkish
Journal Section Research
Authors

Medhini Madi This is me

Shishir Ram Shetty This is me

Subhas G Babu This is me

Sonika Achalli This is me

Publication Date July 22, 2014
Published in Issue Year 2014 Volume: 39 Issue: 3

Cite

MLA Madi, Medhini et al. “Hemifasyal Mikrozomi: Olgu Sunumu Ve Genel Bakış”. Cukurova Medical Journal, vol. 39, no. 3, 2014, pp. 625-3, doi:10.17826/cutf.74086.

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