Sturge - Weber syndrome

Child's Nervous System

Volumn 22, Issue 8, 2006, Pages 909-921

  Di Rocco, C ^a   Tamburrini, Gianpiero ^a  

^a CATHOLIC UNIVERSITY   (Italy)

Author keywords

Epilepsy; Leptomeningeal angiomatosis; Sturge Weber; Surgical treatment

Indexed keywords

ACETYLSALICYLIC ACID; ANTICONVULSIVE AGENT; ANTITHROMBOCYTIC AGENT; CARBAMAZEPINE; PHENOBARBITAL; PHENYTOIN; TOPIRAMATE; VALPROIC ACID;

ARTICLE; CLINICAL FEATURE; CLINICAL TRIAL; COMPUTER ASSISTED TOMOGRAPHY; DISEASE ASSOCIATION; DISEASE CLASSIFICATION; DISEASE CONTROL; ELECTROENCEPHALOGRAPHY; EPILEPSY; HEMISPHERECTOMY; HISTOPATHOLOGY; HUMAN; MONOTHERAPY; NEUROSURGERY; NUCLEAR MAGNETIC RESONANCE IMAGING; OCCLUSIVE CEREBROVASCULAR DISEASE; PATHOGENESIS; POSITRON EMISSION TOMOGRAPHY; POSTOPERATIVE COMPLICATION; PREOPERATIVE EVALUATION; PRIORITY JOURNAL; SINGLE PHOTON EMISSION COMPUTER TOMOGRAPHY; STURGE WEBER SYNDROME; SURGICAL TECHNIQUE; TREATMENT INDICATION; TREATMENT OUTCOME;

DIAGNOSTIC IMAGING; ELECTROENCEPHALOGRAPHY; HUMANS; NEUROSURGICAL PROCEDURES; STURGE-WEBER SYNDROME;

EID: 33746310326     PISSN: 02567040     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00381-006-0143-2     Document Type: Article

References (61)

1. Alexander GL (1972) Sturge-Weber disease. In: Vinken PJ, Bruyn GW (eds) Handbook of clinical neurology. The phakomatoses, vol. 14. Elsevier, New York, pp 223-240
2. Alexander G, Norman RM (1960) The Sturge-Weber Syndrome. J Wright and Sons, Bristol
3. Arzimanoglou A, Aicardi J (1992) The epilepsy of Sturge-Weber syndrome: clinical features and treatment in 23 patients. Acta Neurol Scand 140:S18-S22
4. Arzimanoglou A, Andermann F, Aicardi J, Sainte-Rose C, Beaulieu MA, Villemure JG, Olivier A, Rasmussen Th (2000) Sturge-Weber syndrome. Indications and results of surgery in 20 patients. Neurology 55:1472-1479
5. Bergstrand H, Olivecrona H, Tonnis W (1936) Gefassmissbildungen and gefassgeschwulte des gehrins. Thieme, Leipzig, p 181
6. Chao DHC (1959) Congenital neurocutaneous syndromes of childhood. III. Sturge-Weber disease. J Pediatr 55:635-648
7. Chapieski L, Friedman A, Lachar D (2000) Psychological functioning in children and adolescents with Sturge-Weber syndrome. J Child Neurol 3:181
8. Chugani HT (1994) The role of PET in childhood epilepsy. J Child Neurol 9(1):S82-S88
9. Comi A (2003) Pathophysiology of Sturge-Weber syndrome. J Child Neurol 18:509-516
10. Comi A, Hunt P, Vawter MP, Pardo CA, Becker KG, Pevsner J (2003) Increased fibronectin expression in Sturge-Weber syndrome fibroblasts and brain tissue. Pediatr Res 53(5):762-769
11. Cunha e Sa M, Barroso CP, Caldas MC, Edvinsson L, Gulbenkian S (1997) Innervation pattern of malformative vessels in Sturge-Weber disease: An histochemical. Immunohistochemical and ultrastructural study. Neurosurgery 41(4):872-877
12. Cushing H (1906) Cases of spontaneous intracranial hemorrhage associated with trigeminal nevi. JAMA 47:178-183
13. Dimitri V (1923) Tumor cerebral congénito (angioma cavernosum) Rev Asoc Med Argent 36:1029-1037
14. Di Rocco C (1992) Sturge-Weber disease. In: Raimondi AJ, Choux M, Di Rocco C (eds) Cerebrovascular diseases in children, Springer, Berlin Heidelberg New York, pp 168-187
15. Di Trapani G, Di Rocco C, Abbamonti AL, Caldarelli M (1982) Light microscopy and ultrastructural studies of Sturge-Weber disease. Childs Brain 9:23-36
16. Duncan DB, Herholz K, Pietrzyk U, Heiss WD (1995) Regional cerebral blood flow and metabolism in Sturge-Weber disease. Clin Nucl Med 20(6):522-523
17. Elster AD, Chen MY (1990) MR imaging of Sturge-Weber syndrome: Role of Gadopentate dimeglumine and gradient-echo techniques. AJNR Am J Neuroradiol 11:685-689
18. Falconer MA, Rushworth RG (1960) Treatment of encephalotrigeminal angiomatosis (Sturge-Weber disease) by hemispherectomy. Arch Dis Child 35:433-447
19. Faller L, Lemmer J (2003) Encephalotrigeminal angiomatosis. SADJ 58(9):370-373
20. Goscinski I, Kunicki A (1972) On surgical treatment of Sturge-Weber syndrome. Acta Med Pol 13:229-236
21. Griffiths PD (1996) Sturge-Weber syndrome revisited: The role of neuroradiology. Neuropediatrics 27:284-294
22. 99mTechnetium HMPAO imaging in children with the Sturge-Weber syndrome: A study of nine cases with CT and MRI correlation. Neuroradiology 39:219-224
23. Gururaj AK, Sztriha L, Johansen J, Nork M (2000) Sturge-Weber syndrome without facial nevus: A case report and review of the literature. Acta Pediatr 89:740-743
24. Hoffman HJ, Hendrick EB, Dennis M (1979) Hemispherectomy for Sturge-Weber syndrome. Childs Brain 5:233-248
25. Horita H, Nozaki H, Hamano S, Aihara T (1990) SPECT of the brain in Sturge-Weber syndrome using N-isopropyl-p[123-I]. No To Hattatsu 22:341-348
26. Ichinose T, Tsuyuguchi N, Morino M, Sunada I, Ohata K, Takami T, Shimonishi Y, Kwabe J, Shiomi S, Hara M (2003) Discrepancy between 18F FDG and 11C-methionine positron emission tomography findings in Sturge-Weber syndrome - case report. Neurol Med Chir 43(9):461-464
27. Ito M, Sato K, Ohnuki A, Uto A (1990) Sturge-Weber disease: Operative indications and surgical results. Brain Dev 12(5):473-477
28. Juhasz C, Chugani DC, Muzik O et al (2000) Is epileptogenic cortex truly hypometabolic on interictal positron emission tomography? Ann Neurol 48:89-96
29. Kalischer S (1897) Demonstration des Gehirns eines kindes mit teleangiektasie der linksseitigen gesichts-kopfhaut und hirnoberflache. Berl Klin Wochenschr 34:1059-1067
30. Kossoff EH, Buck C, Freeman JM (2002) Outcomes of 32 hemispherectomies for Sturge-Weber syndrome worldwide. Neurology 59(1):1735-1738
31. Krabbe KH (1934) Facial and meningeal angiomatosis associated with calcification of the brain cortex: A clinical and anatomopathological contribution. A M A Arch Neurol Psych 32:737-755
32. Kuhl DE, Bevilacqua JE, Mishkin MM, Sanders PP (1972) The brain scan in Sturge-Weber syndrome. Radiology 103:621-625
33. Lee JS, Asano E, Muzik O Chugani DC, Juhasz C, Pfund Z, Philip S, Behen M, Chugani HT (2001) Sturge-Weber syndrome: Correlation between clinical course and FDG PET findings. Neurology 57(2):189-195
34. Lin DM, Barker PB, Kraut MA, Comi A (2003) Early characteristics of Sturge-Weber syndrome, shown by perfusion MR imaging and proton MR spectroscopic imaging. AJNR Am J Neuroradiol 24:1912-1915
35. Lund M (1949) On epilepsy in Sturge-Weber disease. Acta Psychiatr Neurol 24:569-586
36. Maria BL (2000) Current management in child neurology. BC Decker, London
37. Maria BL, Neufeld JA, Rosainz LC et al (1998) Central nervous system structure and function in Sturge-Weber syndrome: Evidence of neurologic and radiologic progression. J Child Neurol 13:606-618
38. Moore GJ, Slovis TL, Chugani HT (1998) Proton magnetic resonance spectroscopy in children with Sturge-Weber syndrome. J Child Neurol 13:332-335
39. Muller RA, Chugani HT, Muzik O, Rothermel RD, Chakraborty PK (1997) Language and motor function activate calcified hemisphere in patients with Sturge-Weber syndrome: A positron emission tomography study. J Child Neurol 12(7):431-437
40. Namer IJ, Battaglia F, Hirsch E, Constantinesco A, Marescaux C (2005) Subtraction Ictal SPECT co-registered to MRI (SISCOM) in Sturge-Weber syndrome Clin Nucl Med 30(1):39-40
41. Ongumekan AO, Hwang PA, Hoffman HJ (1989) Sturge-Weber-Dimitri disease. Role of hemispherectomy in prognosis. Can J Neurol Sci 16:78-80
42. Pagni CA, Wildi E (1977) Pathogenetic hypothesis of intracortical calcifications in Sturge-Weber disease. Case report following lobectomy. Mod Probl Paediatr 18:250-257
43. Penfield W (1952) Ablation of abnormal cortex in cerebral palsy. J Neurol Neurosurg Psychiatry 15:73-78
44. Peterman AF, Hayles AB, Dockerty MB, Love JC (1958) Encephalotrigeminal angiomatosis (Sturge-Weber disease) Clinical study of thirty-five cases. JAMA 167:2169-2176
45. Pinton F, Chiron C, Enjolras O, Motte J, Syrota A, Dulac O (1997) Early single photon emission computed tomography in Sturge-Weber syndrome. J Neurol Neurosurg Psychiatry 63:616-621
46. Rappaport ZH (1988) Corpus callosum section in the treatment of intractable seizures in the Sturge-Weber syndrome. Childs Nerv Syst 4:231-232
47. Rasmussen Th, Mathieson G, Le Blanc F (1972) Surgical therapy of typical and a forme fruste variety of the Sturge-Weber syndrome. Schweiz Arch Neurol Psychiatr 111: 393-409
48. Reid DE, Maria BL, Drane WE, Quisling RG, Hoang KB (1997) Central nervous system perfusion and metabolism abnormalities in Sturge-Weber syndrome. J Child Neurol 12:218-222
49. Roach ES (1992) Neurocutaneous syndromes. Pediatr Clin North Am 39:591-620
50. Roach ES, Bodensteiner J (1999) Neurologic manifestations of Sturge-Weber syndrome. In: Bodensteiner JB, Roach ES (eds) Sturge-Weber syndrome. The Sturge-Weber Foundation, Mount Freedom, NJ, pp 27-38
51. Roach ES, Riela AR, Chugani HT et al (1994) Sturge-Weber syndrome. Recommendations for surgery. J Child Neurol 9:190-192
52. Schrimer R (1860) Ein fall von telangiektasie. Albrecht von Graefes. Arch Ophtalmol 7:119-121
53. Sturge WA (1879) A case of partial epilepsy apparently due to a lesion of the vasomotor centers of the brain. Trans Clin Soc Lond 12:162-167
54. Sujansky E, Conradi S (1995) Outcome of Sturge-Weber syndrome in 52 adults. Am J Med Genet 57:35-45
55. Sujansky E, Conradi S (1995) Sturge-Weber syndrome. Age of onset of seizures and glaucoma and the prognosis for affected children. J Child Neurol 10:49-58
56. Tallman B, Tan OT, Morelli JG et al (1991) Location of port-wine stains and the likelihood of ophthalmic and/or central nervous system complications. Pediatrics 87:323-327
57. Thomas-Sohl KA, Vaslow DF, Maria BL (2004) Sturge-Weber Syndrome: A review. Pediatr Neurol 30(5):303-310
58. Tuxhorn IEB, Pannek HW (2002) Epilepsy surgery in bilateral Sturge-Weber syndrome. Pediatr Neurol 26(5):394-397
59. Venes JL, Linder S (1989) Sturge-Weber-Dimitri syndrome. Encephalotrigeminal angiomatosis. In: Edwards MSB, Hoffman HJ (eds) Cerebral vascular disease in children and adolescents. Williams & Wilkins, Baltimore, pp 337-341
60. Ville D, Enjolras O, Chiron C, Dulac O (2002) Prophylactic antiepileptic treatment in Sturge-Weber disease. Seizure 11(3):145-150
61. Weber FP (1922) Right-sided hemi-hypertrophy resulting from right sided congenital spastic hemiplegia. J Neurol Psychopathol 3:134-139