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

Yıl 2017, , 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, , 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

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.