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Year 2014, Volume: 4 Issue: 2, 91 - 94, 02.08.2014

Mehmet Turan Atilla Cayir Huseyin Tan Yusuf Tuzun Hayri Ogul

Abstract

Moyamoya hastalığı internal karotid arterin terminal bölümü ile ana dallarının ilerleyici stenozu ile karekterize sık görülmeyen bir serebrovasküler bir hastalıktır. Geçici iskemik atak, iskemik inme, intrakraniyal kanamalar, nöbetler, baş ağrısı, koreiform hareketler ve kognitif fonksiyon bozukluğu gibi çeşitli semptomları vardır. Burada geçici iskemik atak, sol hemiparezi ve tek taraflı koreiform hareketleri olan 14 yaşına moyamoya hastalığı tanısı konulan bir hasta sunuldu. Koreiform haraketler, ensefaloduroarteriyosinanjiozis operasyonu sonrası iki taraflı ve aşrırı şiddetlendi. Bu şiddetli koreiform hareketler dopamin reseptör blokör tedavisine dramatik cevap verdi.

Keywords

Arteriyovenöz malformasyon kore moya moya hastalığı

References

  • Suzuki J, Kodama N. Moyamoya disease--a review. Stroke; a journal of cerebral circulation. 1983;14(1):104-9.
  • Ikezaki K, Han DH, Kawano T, Kinukawa N, Fukui M. A clinical comparison of definite moyamoya disease between South Korea and Japan. Stroke; a journal of cerebral circulation. 1997;28(12):2513-7.
  • Ibrahimi DM, Tamargo RJ, Ahn ES. Moyamoya disease in children. Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery. 2010;26(10):1297-308.
  • Nagaraja D, Verma A, Taly AB, Kumar MV, Jayakumar PN. Cerebrovascular disease in children. Acta neurologica Scandinavica. 1994;90(4):251-5.
  • Ohaegbulam C, Magge S, Scott R. Pediatric neurosurgery. Surgery of the developing nervous system. McLone DG ed. Philadelphia: Saunders; 2001.
  • Zheng W, Wanibuchi M, Onda T, Liu H, Koyanagi I, Fujimori K, et al. A case of moyamoya disease presenting with chorea. Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery. 2006;22(3):274-8.
  • Walker KG, Wilmshurst JM. An update on the treatment of Sydenham's chorea: the evidence for established and evolving interventions. Therapeutic advances in neurological disorders. 2010;3(5):301-9.
  • Kinboshi M, Inoue M, Kojima Y, Nakagawa T, Kanda M, Shibasaki H. [Elderly case of moyamoya disease presenting with hemichorea]. Rinsho shinkeigaku = Clinical neurology. 2012;52(1):25-9.
  • Matsushima Y, Inaba Y. Moyamoya disease in children and its surgical treatment. Introduction of a new surgical procedure and its follow-up angiograms. Child's brain. 1984;11(3):155-70.
  • Isono M, Ishii K, Kamida T, Inoue R, Fujiki M, Kobayashi H. Long-term outcomes of pediatric moyamoya disease treated by encephalo-duro-arterio-synangiosis. Pediatric neurosurgery. 2002;36(1):14-21.
  • Tripathi P, Tripathi V, Naik RJ, Patel JM. Moya Moya cases treated with encephaloduroarteriosynangiosis. Indian pediatrics. 2007;44(2):123-7.
  • Hayashi K, Horie N, Suyama K, Nagata I. Clinical features and long-term follow-up of quasi-moyamoya disease in children. Pediatric neurosurgery. 2011;47(1):15-21.
  • Ishii K, Fujiki M, Kobayashi H. Invited article: surgical management of Moyamoya disease. Turkish neurosurgery. 2008;18(2):107-13.

Choreiform movements due to pediatric Moyamoya disease - A case report with a dramatic response to therapy

Year 2014, Volume: 4 Issue: 2, 91 - 94, 02.08.2014

Mehmet Turan Atilla Cayir Huseyin Tan Yusuf Tuzun Hayri Ogul

Abstract

Moyamoya hastalığı internal karotid arterin terminal bölümü ile ana dallarının ilerleyici stenozu ile karekterize sık görülmeyen bir serebrovasküler bir hastalıktır. Geçici iskemik atak, iskemik inme, intrakraniyal kanamalar, nöbetler, baş ağrısı, koreiform hareketler  ve kognitif  fonksiyon bozukluğu gibi çeşitli semptomları vardır. Burada geçici iskemik atak, sol hemiparezi ve tek taraflı koreiform hareketleri olan 14 yaşına moyamoya hastalığı tanısı konulan bir hasta sunuldu. Koreiform haraketler, ensefaloduroarteriyosinanjiozis operasyonu sonrası iki taraflı ve aşrırı şiddetlendi. Bu şiddetli koreiform hareketler dopamin reseptör blokör tedavisine dramatik cevap verdi.

 

 

Keywords

Arteriyovenöz malformasyon ;kore; moya moya hastalığı

References

  • Suzuki J, Kodama N. Moyamoya disease--a review. Stroke; a journal of cerebral circulation. 1983;14(1):104-9.
  • Ikezaki K, Han DH, Kawano T, Kinukawa N, Fukui M. A clinical comparison of definite moyamoya disease between South Korea and Japan. Stroke; a journal of cerebral circulation. 1997;28(12):2513-7.
  • Ibrahimi DM, Tamargo RJ, Ahn ES. Moyamoya disease in children. Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery. 2010;26(10):1297-308.
  • Nagaraja D, Verma A, Taly AB, Kumar MV, Jayakumar PN. Cerebrovascular disease in children. Acta neurologica Scandinavica. 1994;90(4):251-5.
  • Ohaegbulam C, Magge S, Scott R. Pediatric neurosurgery. Surgery of the developing nervous system. McLone DG ed. Philadelphia: Saunders; 2001.
  • Zheng W, Wanibuchi M, Onda T, Liu H, Koyanagi I, Fujimori K, et al. A case of moyamoya disease presenting with chorea. Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery. 2006;22(3):274-8.
  • Walker KG, Wilmshurst JM. An update on the treatment of Sydenham's chorea: the evidence for established and evolving interventions. Therapeutic advances in neurological disorders. 2010;3(5):301-9.
  • Kinboshi M, Inoue M, Kojima Y, Nakagawa T, Kanda M, Shibasaki H. [Elderly case of moyamoya disease presenting with hemichorea]. Rinsho shinkeigaku = Clinical neurology. 2012;52(1):25-9.
  • Matsushima Y, Inaba Y. Moyamoya disease in children and its surgical treatment. Introduction of a new surgical procedure and its follow-up angiograms. Child's brain. 1984;11(3):155-70.
  • Isono M, Ishii K, Kamida T, Inoue R, Fujiki M, Kobayashi H. Long-term outcomes of pediatric moyamoya disease treated by encephalo-duro-arterio-synangiosis. Pediatric neurosurgery. 2002;36(1):14-21.
  • Tripathi P, Tripathi V, Naik RJ, Patel JM. Moya Moya cases treated with encephaloduroarteriosynangiosis. Indian pediatrics. 2007;44(2):123-7.
  • Hayashi K, Horie N, Suyama K, Nagata I. Clinical features and long-term follow-up of quasi-moyamoya disease in children. Pediatric neurosurgery. 2011;47(1):15-21.
  • Ishii K, Fujiki M, Kobayashi H. Invited article: surgical management of Moyamoya disease. Turkish neurosurgery. 2008;18(2):107-13.
There are 13 citations in total.

Details

Primary Language English
Journal Section Case Report
Authors

Mehmet Turan

Atilla Cayir This is me

Huseyin Tan This is me

Yusuf Tuzun This is me

Hayri Ogul This is me

Publication Date August 2, 2014
Published in Issue Year 2014 Volume: 4 Issue: 2

Cite

APA Turan, M., Cayir, A., Tan, H., Tuzun, Y., et al. (2014). Choreiform movements due to pediatric Moyamoya disease - A case report with a dramatic response to therapy. Çağdaş Tıp Dergisi, 4(2), 91-94.
AMA Turan M, Cayir A, Tan H, Tuzun Y, Ogul H. Choreiform movements due to pediatric Moyamoya disease - A case report with a dramatic response to therapy. J Contemp Med. August 2014;4(2):91-94.
Chicago Turan, Mehmet, Atilla Cayir, Huseyin Tan, Yusuf Tuzun, and Hayri Ogul. “Choreiform Movements Due to Pediatric Moyamoya Disease - A Case Report With a Dramatic Response to Therapy”. Çağdaş Tıp Dergisi 4, no. 2 (August 2014): 91-94.
EndNote Turan M, Cayir A, Tan H, Tuzun Y, Ogul H (August 1, 2014) Choreiform movements due to pediatric Moyamoya disease - A case report with a dramatic response to therapy. Çağdaş Tıp Dergisi 4 2 91–94.
IEEE M. Turan, A. Cayir, H. Tan, Y. Tuzun, and H. Ogul, “Choreiform movements due to pediatric Moyamoya disease - A case report with a dramatic response to therapy”, J Contemp Med, vol. 4, no. 2, pp. 91–94, 2014.
ISNAD Turan, Mehmet et al. “Choreiform Movements Due to Pediatric Moyamoya Disease - A Case Report With a Dramatic Response to Therapy”. Çağdaş Tıp Dergisi 4/2 (August 2014), 91-94.
JAMA Turan M, Cayir A, Tan H, Tuzun Y, Ogul H. Choreiform movements due to pediatric Moyamoya disease - A case report with a dramatic response to therapy. J Contemp Med. 2014;4:91–94.
MLA Turan, Mehmet et al. “Choreiform Movements Due to Pediatric Moyamoya Disease - A Case Report With a Dramatic Response to Therapy”. Çağdaş Tıp Dergisi, vol. 4, no. 2, 2014, pp. 91-94.
Vancouver Turan M, Cayir A, Tan H, Tuzun Y, Ogul H. Choreiform movements due to pediatric Moyamoya disease - A case report with a dramatic response to therapy. J Contemp Med. 2014;4(2):91-4.