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DESENDAN SEYİRLİ BİR GUİLLAİN BARRE SENDROMU OLGUSU

Year 2011, Volume: 2 Issue: 6, - , 03.03.2015

Abstract

Guillain Barre Sendromu (GBS), sıklıkla simetrik güçsüzlük ve arefleksi ile karakterize akut inflamatuar polinöropatidir. Geçirilmiş bakteriyel veya viral enfeksiyonların tetiklediği otoimmün bir hastalık olduğu kabul edilmektedir. Çocukluk çağı GBS'de mortalite %1-2 oranındadır ve genellikle solunum yetersizliğine bağlı olarak gelişir. Burada 14 yaşında viral enfeksiyon sonrası GBS gelişen bir erkek çocuk sunularak bu sendromun klinik özellikleri gözden geçirildi.Guillain, Barre ve Strohl 1916’da 1.Dünya Savaşı sırasında iki askerde spontan olarak iyileşen progresif motor bozukluk bildirdiler. Benzer olgular daha önce de bildirilmesine rağmen, Guillain ve ark. reflekslerin bir periferik sinir etkilenmesine bağlı olarak kaybolduğunu ve beyin omurilik sıvısında protein artışıyla birlikte hücre sayısının normal oluşuyla Poliomiyelitten farklı bir hastalık olduğunu gösterdiler (1). 

References

  • Winer JB. Guillain-Barré syndrome: clinical variants and their pathogenesis. J Neuroimmunol. 2011; 231: 70-2.
  • Asbury A, Cornblath DR. Assessment of current diagnostic criteria for Guillain-Barre Syndrome. Ann Neurol 1990; 27: 21-4.
  • Ropper AH. The Guillain Barre syndrome. N Engl J Med 1992; 23: 1130-6.
  • McGrogan A, Madle GC, Seaman HE, de Vries CS. The epidemiology of Guillain-Barré syndrome worldwide. A systematic literature review. Neuroepidemiology 2009; 32: 150- 63
  • Rantala H, Uhari M, Niemela M. Occurrence, clinical manifestations, and prognosis of Guillain-Barre Syndrome, Arch Dis Child 1991; 66: 706.
  • Menkes HJ: Immunologically mediated demyelinating diseases of the periferal nervous system, Guillain-Barre Syndrome. In: Menkes HJ,Sarnat BH eds. Textbook of Child Neurology. Philadelphia: Lippincott Williams and Wilkins 2000: 658-65.
  • Kuwaba S, Mori M, Ogawara K et al. Indicators of rapid clinical recovery in Guillain Barre syndome. J Neurol Neurosurg Psychiatry 2001; 70: 560-2.
  • Delanoe C, Sebire G, Landrieu P, Huault G, Metral S. Acute inflammatory demyelinating polyradiculopathy in children: Clinical and electrodiagnostic studies. Ann Neurol 1998; 44: 350-6.
  • Visser LH, van der Meche FG, Meulstee J et al. Cytomegalovirus infection and Guillain- Barre syndrome: The clinical, electrophysiologic, and prognostic features. Dutch Guillain- Barre Study Group. Neurology 1996; 47: 668-73.
  • Yuki N, Ang CW, Koga M, et al. Clinical features and response to treatment in Guillain- Barre Syndrome assosiated with antibodies to GM1b ganglioside Ann Neurol 2000; 47: 314-21.
  • Italian Guillain-Barre Study Group. The prognosis and main prognostic indicators of Guillain Barre syndrome. A multicentre prospective study of 297 patients. Brain 1996; 119: 2053-61.
  • Bradshaw DY, Jones HR Jr. Guillain-Barre syndrome in children: Clinical course, electrodiagnosis, and prognosis. Muscle Nerve 1992; 15: 500-6.
  • Moulin DE, Hagen N, Feasby TE, et al. Pain in Guillain-Barre syndrome. Neurology 1997; 48: 328-31.
  • Larsen A, Tobias JD. Guillain-Barre syndrome presenting with symptoms of upper airway obstruction. Pediatr Emerg Care 1994; 10: 347-8.
  • Briscoe DM, Mc Menamin JB, O'Donohoe NV. Prognosis in Guillain-Barre syndrome Arch Dis Child 1987; 62: 733-5.
  • Jones HR. Childhood Guillain-Barre syndrome: Clinical presentation, diagnosis, and therapy. J Child Neurol 1996; 11: 4-12.

A CASE OF GUILLAIN BARRE SYNDROME WITH DESCENDANT COURSE

Year 2011, Volume: 2 Issue: 6, - , 03.03.2015

Abstract

Guillain Barre Syndrome (GBS) is an acute inflammatory polyneuropathy characterized by symmetrical weakness and areflexia. It is considered to be an autoimmune disease triggered by bacterial or viral infections. The mortality is 1-2% in childhood GBS and it usually develops due to respiratory failure. We present a 14 years old boy with GBS developed after viral infection.

Guillain Barre Syndrome (GBS) is an acute inflammatory polyneuropathy characterized by symmetrical weakness and areflexia. It is considered to be an autoimmune disease triggered by bacterial or viral infections. The mortality is 1-2% in childhood GBS and it usually develops due to respiratory failure. We present a 14 years old boy with GBS developed after viral infection.

References

  • Winer JB. Guillain-Barré syndrome: clinical variants and their pathogenesis. J Neuroimmunol. 2011; 231: 70-2.
  • Asbury A, Cornblath DR. Assessment of current diagnostic criteria for Guillain-Barre Syndrome. Ann Neurol 1990; 27: 21-4.
  • Ropper AH. The Guillain Barre syndrome. N Engl J Med 1992; 23: 1130-6.
  • McGrogan A, Madle GC, Seaman HE, de Vries CS. The epidemiology of Guillain-Barré syndrome worldwide. A systematic literature review. Neuroepidemiology 2009; 32: 150- 63
  • Rantala H, Uhari M, Niemela M. Occurrence, clinical manifestations, and prognosis of Guillain-Barre Syndrome, Arch Dis Child 1991; 66: 706.
  • Menkes HJ: Immunologically mediated demyelinating diseases of the periferal nervous system, Guillain-Barre Syndrome. In: Menkes HJ,Sarnat BH eds. Textbook of Child Neurology. Philadelphia: Lippincott Williams and Wilkins 2000: 658-65.
  • Kuwaba S, Mori M, Ogawara K et al. Indicators of rapid clinical recovery in Guillain Barre syndome. J Neurol Neurosurg Psychiatry 2001; 70: 560-2.
  • Delanoe C, Sebire G, Landrieu P, Huault G, Metral S. Acute inflammatory demyelinating polyradiculopathy in children: Clinical and electrodiagnostic studies. Ann Neurol 1998; 44: 350-6.
  • Visser LH, van der Meche FG, Meulstee J et al. Cytomegalovirus infection and Guillain- Barre syndrome: The clinical, electrophysiologic, and prognostic features. Dutch Guillain- Barre Study Group. Neurology 1996; 47: 668-73.
  • Yuki N, Ang CW, Koga M, et al. Clinical features and response to treatment in Guillain- Barre Syndrome assosiated with antibodies to GM1b ganglioside Ann Neurol 2000; 47: 314-21.
  • Italian Guillain-Barre Study Group. The prognosis and main prognostic indicators of Guillain Barre syndrome. A multicentre prospective study of 297 patients. Brain 1996; 119: 2053-61.
  • Bradshaw DY, Jones HR Jr. Guillain-Barre syndrome in children: Clinical course, electrodiagnosis, and prognosis. Muscle Nerve 1992; 15: 500-6.
  • Moulin DE, Hagen N, Feasby TE, et al. Pain in Guillain-Barre syndrome. Neurology 1997; 48: 328-31.
  • Larsen A, Tobias JD. Guillain-Barre syndrome presenting with symptoms of upper airway obstruction. Pediatr Emerg Care 1994; 10: 347-8.
  • Briscoe DM, Mc Menamin JB, O'Donohoe NV. Prognosis in Guillain-Barre syndrome Arch Dis Child 1987; 62: 733-5.
  • Jones HR. Childhood Guillain-Barre syndrome: Clinical presentation, diagnosis, and therapy. J Child Neurol 1996; 11: 4-12.
There are 16 citations in total.

Details

Primary Language Turkish
Subjects Health Care Administration
Journal Section Case Report
Authors

Fatmagül Başarslan This is me

Cahide Yılmaz This is me

Murat Tutanç This is me

Vefik Arıca This is me

Nilgün Üstün This is me

Işıl Davarcı This is me

Publication Date March 3, 2015
Submission Date February 28, 2015
Published in Issue Year 2011 Volume: 2 Issue: 6

Cite

Vancouver Başarslan F, Yılmaz C, Tutanç M, Arıca V, Üstün N, Davarcı I. DESENDAN SEYİRLİ BİR GUİLLAİN BARRE SENDROMU OLGUSU. mkutfd. 2015;2(6).