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Coexistence of Chiari malformation type I and isolated hemihypertrophy in a 15-year old girl: a case report

Yıl 2017, Cilt: 8 Sayı: 3, 101 - 104, 30.09.2017
https://doi.org/10.5799/jcei.343203

Öz

Hemihypertrophy is the asymmetrical growth of one or more parts of the body, and might be
either isolated or a component of various syndromes. Coexistence of isolated hemihypertrophy
and Chiari malformation type I are very rarely. In this study, our objective was to present a 15
years old girl case with isolated hemihypertrophy and Chiari malformation type I in the light of
literature data. 

Kaynakça

  • 1. Heilstedt HA, Bacino CA. A case of familial isolated hemihyperplasia. BMC Medical Genetics 2004;10:2350-5.
  • 2. Hoyme HE, Seaver LH, Jones KL, et al. Isolated hemihyperplasia (hemihypertrophy); report of a prosoective multicenter study of the incidence of neoplasia and reviw. Am J Med Genel 1998;79:274-8.
  • 3. Pettorini BL, Oesman C, magdun S. New presenting symptoms of chiari 1 malformation: report two cases. Childs Nerv Syst 2010;26:399-402.
  • 4. Benjamin MD, Santiago J, Hebert JC, et. al. Hemihypertrophy and scoliosis revealing a Chiari 1 malformation with syringomyelia. Arch Pediatr. 2011;18:1210-5.
  • 5. Rowe NH. Hemifacial hypertrophy. Review of the literature and addition of four cases. Oral Surg Oral Med Oral Pathol 1962;15:572-87
  • 6. Gorlin RJ. Proteus syndrome. J Clin Dysmorphol 1984;2:8-9.
  • 7. Viljoen DL. Klippel-Trenaunay-Weber syndrome (angio-macroglossiajigantism syndrome). J Med Genet 1988;25:250-2.
  • 8. Gorlin RJ, Meskin LH. Congenital hemihypertrophy. Review of the literature and report of a case with special emphasis on oral manifestations. J Pediatr 1962;61:870-9.
  • 9. Ringrose RE, Jabbour JT, Keele DK. Hemihypertrophy. Pediatrics 1965;36:434-48.
  • 10. Milhorat TH, Chou MW, Trinidad EM et al. Chiari I malformation redefined clinical and radiographic findings for 364 symptomatic patients. Neurosurgery 1999;44:1005-17.
  • 11. Novegno F, Caldarelli M, Massa A et al. The natural history of the Chiari type I anomaly. J Neurosurg Pediatr 2008;2:179-87
  • 12. Park JK, Gleason PL, Madsen JR, Goumnerova LC, Scott RM. Presentation and management of Chiari I malformation in children. Pediatr Neurosurg 1997;26:190-6.
  • 13. Tubbs RS, Mc Girt MJ, Oakes WJ. Surgical experience in 130 pediatric patients with Chiari I malformations. J Neurosurg 2003;99:291-6
  • 14. Tubbs RS, Smyth MD, Wellons JC. et al. Hemihypertrophy and the Chiari I malformation. Pediatr Neurosurgery 2003;38:258-61.
  • 15. Lapresle J, Métreau R, Risvegliato M. Segmental muscular hypertrophy in Arnold Chiari deformity associated with syringomyelia syndrome (article in French). Rev Neurol 1976;132:567-70.
  • 16. Udayakumaran S, Onyia CU. Beckwith-Wiedemann syndrome and Chiari I malformation--a case-based review of central nervous system involvement in hemihypertrophy syndromes. Childs Nerv Syst. 2015;31:637-41.
Yıl 2017, Cilt: 8 Sayı: 3, 101 - 104, 30.09.2017
https://doi.org/10.5799/jcei.343203

Öz

Kaynakça

  • 1. Heilstedt HA, Bacino CA. A case of familial isolated hemihyperplasia. BMC Medical Genetics 2004;10:2350-5.
  • 2. Hoyme HE, Seaver LH, Jones KL, et al. Isolated hemihyperplasia (hemihypertrophy); report of a prosoective multicenter study of the incidence of neoplasia and reviw. Am J Med Genel 1998;79:274-8.
  • 3. Pettorini BL, Oesman C, magdun S. New presenting symptoms of chiari 1 malformation: report two cases. Childs Nerv Syst 2010;26:399-402.
  • 4. Benjamin MD, Santiago J, Hebert JC, et. al. Hemihypertrophy and scoliosis revealing a Chiari 1 malformation with syringomyelia. Arch Pediatr. 2011;18:1210-5.
  • 5. Rowe NH. Hemifacial hypertrophy. Review of the literature and addition of four cases. Oral Surg Oral Med Oral Pathol 1962;15:572-87
  • 6. Gorlin RJ. Proteus syndrome. J Clin Dysmorphol 1984;2:8-9.
  • 7. Viljoen DL. Klippel-Trenaunay-Weber syndrome (angio-macroglossiajigantism syndrome). J Med Genet 1988;25:250-2.
  • 8. Gorlin RJ, Meskin LH. Congenital hemihypertrophy. Review of the literature and report of a case with special emphasis on oral manifestations. J Pediatr 1962;61:870-9.
  • 9. Ringrose RE, Jabbour JT, Keele DK. Hemihypertrophy. Pediatrics 1965;36:434-48.
  • 10. Milhorat TH, Chou MW, Trinidad EM et al. Chiari I malformation redefined clinical and radiographic findings for 364 symptomatic patients. Neurosurgery 1999;44:1005-17.
  • 11. Novegno F, Caldarelli M, Massa A et al. The natural history of the Chiari type I anomaly. J Neurosurg Pediatr 2008;2:179-87
  • 12. Park JK, Gleason PL, Madsen JR, Goumnerova LC, Scott RM. Presentation and management of Chiari I malformation in children. Pediatr Neurosurg 1997;26:190-6.
  • 13. Tubbs RS, Mc Girt MJ, Oakes WJ. Surgical experience in 130 pediatric patients with Chiari I malformations. J Neurosurg 2003;99:291-6
  • 14. Tubbs RS, Smyth MD, Wellons JC. et al. Hemihypertrophy and the Chiari I malformation. Pediatr Neurosurgery 2003;38:258-61.
  • 15. Lapresle J, Métreau R, Risvegliato M. Segmental muscular hypertrophy in Arnold Chiari deformity associated with syringomyelia syndrome (article in French). Rev Neurol 1976;132:567-70.
  • 16. Udayakumaran S, Onyia CU. Beckwith-Wiedemann syndrome and Chiari I malformation--a case-based review of central nervous system involvement in hemihypertrophy syndromes. Childs Nerv Syst. 2015;31:637-41.
Toplam 16 adet kaynakça vardır.

Ayrıntılar

Konular Sağlık Kurumları Yönetimi
Bölüm Olgu Sunumu
Yazarlar

Halil Kazanasmaz

Mustafa Calik

Yayımlanma Tarihi 30 Eylül 2017
Yayımlandığı Sayı Yıl 2017 Cilt: 8 Sayı: 3

Kaynak Göster

APA Kazanasmaz, H., & Calik, M. (2017). Coexistence of Chiari malformation type I and isolated hemihypertrophy in a 15-year old girl: a case report. Journal of Clinical and Experimental Investigations, 8(3), 101-104. https://doi.org/10.5799/jcei.343203
AMA Kazanasmaz H, Calik M. Coexistence of Chiari malformation type I and isolated hemihypertrophy in a 15-year old girl: a case report. J Clin Exp Invest. Eylül 2017;8(3):101-104. doi:10.5799/jcei.343203
Chicago Kazanasmaz, Halil, ve Mustafa Calik. “Coexistence of Chiari Malformation Type I and Isolated Hemihypertrophy in a 15-Year Old Girl: A Case Report”. Journal of Clinical and Experimental Investigations 8, sy. 3 (Eylül 2017): 101-4. https://doi.org/10.5799/jcei.343203.
EndNote Kazanasmaz H, Calik M (01 Eylül 2017) Coexistence of Chiari malformation type I and isolated hemihypertrophy in a 15-year old girl: a case report. Journal of Clinical and Experimental Investigations 8 3 101–104.
IEEE H. Kazanasmaz ve M. Calik, “Coexistence of Chiari malformation type I and isolated hemihypertrophy in a 15-year old girl: a case report”, J Clin Exp Invest, c. 8, sy. 3, ss. 101–104, 2017, doi: 10.5799/jcei.343203.
ISNAD Kazanasmaz, Halil - Calik, Mustafa. “Coexistence of Chiari Malformation Type I and Isolated Hemihypertrophy in a 15-Year Old Girl: A Case Report”. Journal of Clinical and Experimental Investigations 8/3 (Eylül 2017), 101-104. https://doi.org/10.5799/jcei.343203.
JAMA Kazanasmaz H, Calik M. Coexistence of Chiari malformation type I and isolated hemihypertrophy in a 15-year old girl: a case report. J Clin Exp Invest. 2017;8:101–104.
MLA Kazanasmaz, Halil ve Mustafa Calik. “Coexistence of Chiari Malformation Type I and Isolated Hemihypertrophy in a 15-Year Old Girl: A Case Report”. Journal of Clinical and Experimental Investigations, c. 8, sy. 3, 2017, ss. 101-4, doi:10.5799/jcei.343203.
Vancouver Kazanasmaz H, Calik M. Coexistence of Chiari malformation type I and isolated hemihypertrophy in a 15-year old girl: a case report. J Clin Exp Invest. 2017;8(3):101-4.