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

Year 2017, Volume: 8 Issue: 3, 101 - 104, 30.09.2017

Halil Kazanasmaz , Mustafa Calik

https://doi.org/10.5799/jcei.343203

Abstract

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. 

Keywords

Hemihypertrophy, Chiari malformation type I, child, syndrome

References

• 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.