Título: Neurologic Manifestations of Childhood Rheumatic Diseases
Autores: SHIARI, Reza; Associate Professor of Pediatric Rheumatology, Department of Pediatric Rheumatology, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran- Iran
Fecha: 2013-01-01
Publicador: Iranian Journal of Child Neurology
Fuente:
Tipo: info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion


Tema: Neurologic manifestations; Systemic Lupus erythematosus; Kawasaki disease; Seizures; Aseptic meningitis
Descripción: How to Cite this Article: Shiari R. Neurologic Manifestations of Childhood Rheumatic Diseases.  Iran J Child Neurol Autumn 2012; 6(4): 1-7.Children with rheumatic disorders may have a wide variety of clinical features ranging from fever or a simple arthritis to complex multisystem autoimmune diseases. Information about the prevalence of neurological manifestations in children with rheumatologic disorders is limited. This review describes the neurologic complications of childhood Rheumatic disease either solely or combined with symptoms of other organs involvement, as a primary manifestation or as a part of other symptoms, additionally. References1. Benseler S, Schneider R. Central nervous system vasculitisin children. Curr Opin Rheumatol. 2004 Jan;16(1):43-50. 2. Benseler SM. Central nervous system vasculitis in children. Curr Rheumatol Rep. 2006 Dec;8(6):442-9. 3. Mc Carthy HJ, Tizard EJ. Clinical practice: Diagnosis and management of Henoch-Schönlein purpura. Eur J Pediatr.2010 Jun;169(6):643-50. Epub 2009 Dec 12. 4. Robson WL, Leung AK. Henoch-Schönlein purpura. AdvPediatr. 1994;41:163-94. 5. Ostergaard JR, Storm K, Neurologic manifestations of Schönlein-Henoch purpura. Acta Paediatr Scand. 1991Mar;80(3):339-42. 6. Bakkaloğlu SA, Ekim M, Tümer N, Deda G, ErdenI, Erdem T. Cerebral vasculitis in Henoch-Schönlein purpura. Nephrol. Dial Transplant. 2000 Feb;15(2):246-8. 7. Mattoo TK, al-Mutair A, al-Khatib Y, Ali A, al-SohaibaniMO. Group A beta-haemolytic streptococcal infection and Henoch-Schonlein purpura with cardiac, renal and neurological complications. Ann Trop Pediatr. 1997Dec;17(4):381-6. 8. Ha TS, Cha SH. Cerebral vasculitis in Henoch-Schönlein purpura: a case with sequential magnetic resonance imaging. Pediatr Nephrol. 1996;10:634-6. 9. Saket S, Mojtahedzadeh S, Karimi A, Shiari R, ShirvaniF. Relationship between electrolyte abnormalities, ESR,CRP and platelet count with severity of Kawasaki disease.Yafteh. 2009;11(3):5-14. 10. Halimiasl A, Hosseini AH, Shiari R, Ghadamli P,Mojtahedzadeh S. Concomitant Coronary Artery Aneurysm and Myocarditis as a Rare Manifestation of Kawasaki Disease: A Case Report. J Compr Ped.2012;3(1):34-6. 11. Ichiyama T, Nishikawa M, Hayashi T, Koga M, Tashiro N, Furukawa S. Cerebral hypoperfusion during acute Kawasaki disease. Stroke. 1998 Jul;29(7):1320-1. 12. Muneuchi J, Kusuhara K, Kanaya Y, Ohno T, Furuno K,Kira R, Mihara F, Hara T. Magnetic resonance studies of brain lesions in patients with Kawasaki disease. Brain Dev. 2006 Jan;28(1):30-3. 13. Scolding NJ, Wilson H, Hohlfeld R, Polman C, Leite I,Gilhus N. The recognition, diagnosis and management of cerebral vasculitis: a European survey. Eur J Neurol. 2002Jul;9(4):343-7. 14. Guillevin L, Durand-Gasselin B, Cevallos R, Gayraud M, Lhote F, Callard P et al. Microscopic polyangiitis:clinical and laboratory findings in eighty-five patients.Arthritis Rheum. 1999 Mar;42(3):421-30. 15. Rahman A, Isenberg DA. Systemic lupus erythematosus.N Engl J Med. 2008 Feb;358(9):929-39. 16. Farivar S, Shiari R, Nejad Hosseinian M, Eshtad S. New genetic finding in systemic lupus erythematosus. Genet inthe 3rd Millen 2008;6(2):1333-8. 17. Sibbitt WL Jr, Brandt JR, Johnson CR, Maldonado ME,Patel SR, Ford CC et al. The incidence and prevalence of neuropsychiatric syndromes in pediatric onset systemic lupus erythematosus. J Rheumatol. 2002 Jul;29(7):1536-42. 18. Harel L, Sandborg C, Lee T, von Scheven E.Neuropsychiatric manifestations in pediatric systemic lupus erythematosus and association with antiphospholipid antibodies. J Rheumatol. 2006 Sep;33(9):1873-7. 19. Hawro T, Bogucki A, Sysa-Jedrzejowska A, BogaczewiczJ, Wozniacka A. [Neurological disorders in systemic lupus erythematosus patients]. Pol Merkur Lekarski. 2009 Jan;26(151):43-8. 20. Greenberg BM. The neurologic manifestations of systemic lupus erythematosus. Neurologist. 2009May;15(3):115-21.21. Sofat N, Malik O, Higgens CS. Neurological involvementin patients with rheumatic disease. QJM 2006 Feb;99(2):69-79. 22. Shiari R, Farivar S. Juvenile Systemic Lupus Erythematosus associated with Klinefelter’s syndrome: A case report. Reumatol Clin. 2010 Jul-Aug;6(4):212-3. 23. Yuan H, Ni JD, Pan HF, Li LH, Feng JB, Ye DQ. Lack of association of FcyRIIIb polymorphisms with systemic lupus erythematosus: a meta-analysis. Rheumatol Int.2011 Aug;31(8):1017-21. 24. Shiari R, Kobayashi I, Toita N, Hatano N, Kawamura N, Okano M et al. Epitope mapping of anti-alpha-fodrinauto antibody in juvenile Sjögren’s syndrome: differencein major epitopes between primary and secondary cases. J Rheumatol. 2006 Jul;33(7):1395-400. 25. Ozen S. Pediatric onset Behçet disease. Curr Opin Rheumatol. 2010 Sep;22(5):585-9. 26. Wadia N, Williams E. Behçet’s syndrome with neurological complications. Brain. 1957 Mar;80(1):59-71. 27. Ai-Araji A, Kidd DP. Neuro-Behçet’s disease:epidemiology, clinical characteristics, and management.Lancet Neurol. 2009 Feb;8(2):192-204. 28. Namer IJ, Karabudak R, Zileli T, Ruacan S, KücükaliT, Kansa E. Peripheral nervous systems involvement inBehçet’s disease. Case report and review of the literature.Eur Neurol. 1987;26(4):235-240. 29. Takeuchi A, Kodama M, Takatsu M, Hashimoto T,Miyashita H. Mononeuritis multiplex in incompleteBehçet’s disease a case report and the review of theliterature. Clin Rheumatol 1989 Sep;8(3):375-380. 30. Aksoyek S, Aytemir K, Ozer N, Ozcebe O, Oto A.Assessment of autonomic nervous system functionin patients with Behçet’s disease by spectral analysisof heart rate variability. J Auton Nerv Syst. 1999 Sep24;77(2):190-4. 31. Borhani-Haghighi A, Samangooie S, Ashjazadeh N,Nikseresht, A Shariat A, Yousefipour G et al. Neurological manifestations of Behçet’s disease. Neurosciences(Riyadh). 2006 Oct;11(4):260-4. 32. Ideguchi H, Suda A, Takeno M, Kirino Y, Ihata A,Ueda A et al. Neurological manifestations of Behçet’s disease in Japan: a study of 54 patients. J Neurol. 2010 Jun;257(6):1012-20. Epub 2010 Feb 3. 33. Cassidy JT, Levinson JE, Bass JC, Baum J, Brewer EJJr., Fink CW et al. A study of classification criteria fora diagnosis of juvenile rheumatoid arthritis. Arthritis Rheum. 1986 Feb;29(2):274-81. 34. Ravelli A, Martini A. Juvenile idiopathic arthritis.Lancet. 2007 Mar 3;369(9563):767-78. 35. Farivar S, Shiari R, Hadi E. Genetic susceptibility tojuvenile idiopathic arthritis in Iranian children. Arch Med Res. 2011 May;42(4):301-4. 36. Unal O, Ozçakar L, Cetin A, Kaymak B. Severe bilateral carpal tunnel syndrome in juvenile chronic arthritis.Pediatr Neurol. 2003 Oct;29(4):345-8. 37. Ueno H, Katamura K, Hattori H, Yamaguchi Y,Nakahata T. Acute lethal encephalopathy in systemic juvenile rheumatoid arthritis. Pediatr Neurol. 2002 Apr;26(4):315-7. 38. Duzova A, Bakkaloglu A. Central nervous system involvement in pediatric rheumatic diseases:current concepts in treatment. Curr Pharm Des.2008;14(13):1295-301. 39. Laiho K, Savolainen A, Kautiainen H, Kekki P, Kauppi M. The cervical spine in juvenile chronic arthritis. Spine J. 2002 Mar-Apr;2(2):89-94. 40. De Cunto CL, Liberatore DI, San Román JL, Goldberg JC, Morandi AA, Feldman G. Infantile-onset multisystem inflammatory disease: a differential diagnosis of systemic juvenile rheumatoid arthritis. J Pediatr. 1997 Apr;130(4):551-6. 41. Farivar S, Shiari R, Hadi E. Molecular analysis of MEFV gene in Iranian children with familial Mediterranean fever. Ind J Rheumato. 2010 Jun;5(2):66-8. 42. Kalyoncu U, Eker A, Oguz KK, Kurne A, Kalan I,Topcuoglu AM et al. Familial Mediterranean fever and central nervous system involvement: a case series. Medicine (Baltimore). 2010 Mar;89(2):75-84. 43. Radice A, Sinico RA. Antineutrophil cytoplasmic antibodies (ANCA). Autoimmunity. 2005 Feb;38(1):93-103. 44. Nishino H, Rubino FA, DeRemee RA, Swanson JW,Parisi JE. Neurological involvement in Wegener’s granulomatosis: an analysis of 324 consecutive patients at the Mayo Clinic. Ann Neurol. 1993 Jan;33(1):4-9. 45. Masi AT, Hunder GG, Lie JT, Michel BA, Bloch DA,Arend WP et al. The American College of Rheumatology1990 criteria for the classification of Churg-Strauss syndrome (allergic granulomatosis and angiitis).Arthritis Rheum. 1990 Aug;33(8):1094-100. 46. Sehgal M, Swanson JW, DeRemee RA, Colby TV.Neurologic manifestations of Churg-Strauss syndrome.Mayo Clin Proc. 1995 Apr;70(4):337-41. 47. Twardowsky AO, Paz JA, Pastorino AC, Jacob CM,Marques-Dias MJ, Silva CA. Chorea in a child with Churg-Strauss syndrome. Acta Reumatol Port. 2010 Jan-Mar;35(1):72-5. 48. Kumar N, Vaish AK. Hemiplegia due to Churg Strauss syndrome in a young boy. J Assoc Physicians India.2011 Mar;59:172-3. 49. Pagnoux C, Seror R, Henegar C, Mahr A, Cohen P,Le Guern V et al. Clinical features and outcomes in 348 patients with polyarteritis nodosa: a systematic retrospective study of patients diagnosed between 1963 and 2005 and entered into the French Vasculitis Study Group Database. Arthritis Rheum. 2010 Feb;62(2):616-26. 50. Valeyrie L, Bachot N, Roujeau JC, Authier J, Gherardi R,Hosseini H. Neurological manifestations of polyarteritis nodosa associated with the antiphospholipid syndrome.Ann Med Interne (Paris). 2003 Nov;154(7):479-82. 51. Cellucci T, Benseler SM. Diagnosing central nervous system vasculitis in children. Curr Opin Pediatr. 2010 Dec;22(6):731-8. 52. Matsell DG, Keene DL, Jimenez C, Humphreys P. Isolated angiitis of the central nervous system in childhood. Can J Neurol Sci. 1990 May;17(2):151-4. 53. Calabrese LH, Furlan AJ, Gragg LA, Ropos TJ. Primary angiitis of the central nervous system: diagnostic criteria and clinical approach. Cleve Clin J Med. 1992 May- Jun;59(3):293-306. 54. Cekinmez EK, Cengiz N, Erol I, Kizilkilic O, Uslu Y. Unusual cause of acute neurologic deficit in childhood: primary central nervous system vasculitis presenting with basilar arterial occlusion. Childs Nerv Syst. 2009 Jan;25(1):133-6. 55. Benseler SM, Silverman E, Aviv RI, Schneider R, Armstrong D, Tyrrell PN. Primary central nervous system vasculitis in children. Arthritis Rheum. 2006 Apr;54(4):1291-7. 56. Yaari R, Anselm IA, Szer IS, Malicki DM, Nespeca MP, Gleeson JG. Childhood primary angiitis of the central nervous system: two biopsy-proven cases. J Pediatr.2004 Nov;145(5):693-7.    
Idioma: Inglés

Artículos similares:

EFFECTS OF ORAL IRON SUPPLEMENT ON BREATH-HOLDING SPELLS IN CHILDREN por TONEKABONI MD, S.H.; Pediatric Neurologist, Assistant Professor of Shaheed Beheshti University of Medical Sciences Child neurology department, Mofid Children’s Hospital,ALAVI MD, S.; Assisstant professor ,Shaheed Beheshti Medical Sciences University, Mofid Children’s Hospital,MAHVELATI MD, F.; Pediatric Neurologist, Assistant Professor of Shaheed Beheshti University of Medical Sciences Child neurology department, Mofid Children’s Hospital,TABASI MD, Z.; Pediatrician
A STUDY ON THE RISK FACTORS FOR OBSTETRICAL BRACHIAL PLEXUS PALSY por ASHRAFZADEH, Farah; Professor of Pediatric Neurology Mashhad University of Medical Sciences, Mashhad, Iran,BOSKABADI, Hasan; Associate Professor of Neonatology, Mashhad University of Medical Sciences, Mashhad, Iran,FARAJI RAD, Mohammad; Professor of Neurosurgery Mashhad University of Medical Sciences, Mashhad, Iran,SEYYED HOSSEINEE, Parisa; Medical student, Mashhad University of Medical Sciences, Mashhad, Iran
Epilepsy as a Rare Neurologic Manifestation of Oculodentodigitalis Dysplasia por BARZEGAR, Mohammad; Professor of pediatric Neurology, Pediatric Health Research Center, Tabriz University of Medical Sciences, Tabriz, Iran,SAYADNASIRI, Mohammad; Assistant professor of Neurology, Department of Neurology, Qazvin University of Medical Sciences, Qazvin, Iran,TABRIZI, Aidin; Pediarician, Pediatric Health Research Center, Tabriz University of Medical Sciences,Tabriz, Iran
Role and Function of Mitochondria por ZAMANI, Gholamreza; Pediatric Neurology Department, Children’s Medical Center, Tehran University of Medical Sciences, Tehran, Iran
Lysosomal Storage Disease in Iran (Report of Molecular Study) por HOUSHMAND, Massoud; 1. Assistant Professor of Human Molecular Genetics, Department of Medical Genetic, National Institute for Genetic Engineering and Biotechnology, Tehran, Iran,TONEKABONI, Seyed Hassan; 2.Professor of Pediatric Neurology, Pediatric Neurology Research Center, Shahid Beheshti University of Medical sciences,Tehran, Iran,KARIMZADEH, Parvaneh; Professor of Pediatric Neurology, Pediatric Neurology Research Center, Shahid Beheshti University of Medical sciences,Tehran, Iran,ARYANi, Omid; Genetic Counselor, Medical Genetic Dep. Special Medical Center, Tehran, Iran,ASHRAFI, Mahmoudreza; Professor of Pediatric Neurology, Growth and Development Research Center, Children´s Medical Center, Tehran University of Medical Science, Tehran, Iran,SALEHPOUR, Shadab; Associate Professor of Pediatric Endocrinology and Metabolism, Shahid Beheshti University of Medical Sciences, Tehran, Iran,BADV, Shervin; Assistant Professor of Pediatric Neurology, Zanjan University of Medical Sciences, Zanjan, Iran,SHAKIBA, Marjan; Associate Professor of Pediatric Endocrinology and Metabolism, Shahid Beheshti University of Medical Sciences, Tehran, Iran,ALAEE, Mohammad Reza; Associate Professor of Endocrinology, Shahid Beheshti University of Medical Sciences (SBMU), Tehran, Iran,FARSHIDI, Shahla; Nasle Omid Hope Foundation
GRISCELLI SYNDROME; A CASE REPORT AND REVIEW OF THE LITERATURE por Shamsian MD, B.Sh.; Assistant professor, Department of pediatric hematology-oncology,Mofid children's hospital,Shaid BEheshti Medical University,Arzanian MD, M.T.; Assistant professor ,Cheif of hematology-oncology ward, Department of pediatric hematology-oncology, Shaid Beheshti Medical University,Alavi MD, S.; Assistant professor, Department of pediatric hematology-oncology, Namazi Hospital, Shiraz University of medical sciences,Zareifar MD, S.; Assistant professor, Department of pediatric hematology-oncology, Namazi Hospital, Shiraz University of medical sciences
Downward Vertical Gaze Palsy As A Prominent Manifestation Of Episodic Ataxia Type 2: A Case Report por SHERVIN BADV, Reza; 1. Pediatric Neurologist, Department of Pediatrics, Zanjan University of Medical Sciences, Zanjan, Iran,NIKSIRAT, Ali; 2. Legal Medicine Research Center, Legal Medicine Organization, Tehran, Iran
ETHYLMALONIC ACIDURIA AND REPORT OF ONE CASE FROM IRAN por KARIMZADEH, Parvaneh; Associate Professor of Pediatric Neurology, Pediatric Neurology Research Center, ShahidBeheshti University of Medical Sciences, Mofid Children Hospital, Tehran, Iran
NEONATAL SEIZURE: ETIOLOGY AND TYPE por Moayedi, A.R.; Pediatric Neurologist,Assistant Professor, Hormozgan University of Medical Sciences,Bandar Abbas,Zakeri, S.; Pediatrician, Hormozgan University of Medical Sciences,Moayedi, F.; General Physician
10 
EFFECT OF SENSORY INTEGRATION THERAPY ON GROSS MOTOR FUNCTION IN CHILDREN WITH CEREBRAL PALSY por Shamsoddini, A.R.; Master of Occupational therapy, Baqiyatallah university of Medical Sciences, Medical Faculty.,Hollisaz, M.T.; Professor of Physical Medicine and Rehabilitation, Baqiyatallah university of Medical Sciences, Medical Faculty.