Sturge-weber syndrome: Soft-tissue and skeletal overgrowth

Journal of Craniofacial Surgery

Volumn 20, Issue SUPPL. 1, 2009, Pages 617-621

  Greene, Arin K ^a   Taber, Sarah F ^a   Ball, Karen L ^a   Padwa, Bonnie L ^a   Mulliken, John B ^a  

^a BOSTON CHILDREN S HOSPITAL   (United States)

Author keywords

Bone; Face; Hypertrophy; Overgrowth; Pyogenic granuloma; Soft tissue; Sturge Weber syndrome

Indexed keywords

ADOLESCENT; ADULT; AGED; ARTICLE; CHILD; CONTROL GROUP; CONTROLLED STUDY; FACE MALFORMATION; FEMALE; HUMAN; HYPERTROPHY; LIPOHYPERTROPHY; MAJOR CLINICAL STUDY; MALE; MORBIDITY; PREVALENCE; PRIORITY JOURNAL; QUESTIONNAIRE; SKELETAL OVERGROWTH; SKIN DEFECT; SOFT TISSUE HYPERTROPHY; STURGE WEBER SYNDROME;

ADOLESCENT; ADULT; AGED; COHORT STUDIES; FACE; FACIAL BONES; FEMALE; HUMANS; HYPERTROPHY; LOGISTIC MODELS; MALE; MIDDLE AGED; QUESTIONNAIRES; RETROSPECTIVE STUDIES; STURGE-WEBER SYNDROME; YOUNG ADULT;

EID: 68249084848     PISSN: 10492275     EISSN: None     Source Type: Journal    
DOI: 10.1097/SCS.0b013e318192988e     Document Type: Article

References (29)

1. Sturge WA. A case of partial epilepsy apparently due to a lesion of one of the motor centers of the brain. Trans Clin Soc London 1879;12:112
2. Parkes Weber F. Right-sided hemihypertrophy resulting from right-sided congenital spastic hemiplegia with a morbid condition of the left side of the brain revealed by radiogram. J Neurol Neurosurg Psychiatry 1922;37:301-311
3. Thomas-Sohl KA, Vaslow DF, Maria BL. Sturge-Weber syndrome: a review. Pediatr Neurol 2003;30:303-310
4. Comi AM. Pathophysiology of Sturge-Weber syndrome. J Child Neurol 2003;18:509-516
5. Sujansky E, Conradi S. Outcome of Sturge-Weber syndrome in 52 adults. Am J Med Genet 1995;57:35-45
6. Klapper J. Headache in Sturge-Weber syndrome. Headache 1994;34: 521-522
7. Kossof EH, Buck C, Freeman JM. Outcomes of 32 hemispherectomies for Sturge-Weber syndrome worldwide. Neurology 2002;59: 1735-1738
8. Kossoff EH, Hatfield LA, Ball KL, et al. Comorbidity of epilepsy and headache in patients with Sturge-Weber Syndrome. J Child Neurol 2005;20:678-682
9. Bebin EM, Gomez MR. Prognosis in Sturge-Weber disease: comparison of unihemispheric and bihemispheric involvement. J Child Neurol 1988;3:181-184
10. Oakes WJ. The natural history of patients with the Sturge-Weber syndrome. Pediatr Neurosurg 1992;18:287-290
11. Pascual-Castroviejo I, Diaz-Gonzalez C, Garcia-Melian RM. Sturge-Weber syndrome: study of 40 patients. Pediatr Neurol 1993;9: 283-288
12. Sujansky E, Conradi S. Sturge-Weber syndrome. Age of onset of seizures and glaucoma and the prognosis for affected children. J Child Neurol 1995;10:49-58
13. Baselga E. Sturge-Weber syndrome. Semin Cutan Med Surg 2004;23: 87-98
14. Sullivan TJ, Clarke MP, Morin JD. The ocular manifestations of the Sturge-Weber syndrome. J Pediatr Ophthalmol Strabismus 1992;29: 349-356
15. Hagiwara K, Uezato H, Nonaka S. Phacomatosis pigmentovascularis type IIb associated with Sturge-Weber syndrome and pyogenic granuloma. J Dermatol 1998;25:721-729
16. Klapman MH, Yao JF. Thickening and nodules in port-wine stains. J Am Acad Dermatol 2001;44:300-302
17. Sheehan DJ, Lesher JL. Pyogenic granuloma arising within a port-wine stain. Cutis 2004;73:175-180
18. Mills SE, Cooper PH, Fechner RE. Lobular capillary hemangioma: the underlying lesion of pyogenic granuloma. Am J Surg Pathol 1980;4: 471-479
19. Mills CM, Lanigan SW, Hughes J, et al. Demographic study of port wine stain patients attending a laser clinic: family history, prevalence of naevus anaemicus and results of prior treatment. Clin Exp Dermatol 1997;22:166-168
20. Barsky SH, Rosen S, Geer DE, et al. The nature and evolution of port-wine stains: a computer-assisted study. J Invest Dermatol 1980;74: 154-157
21. Finley JL, Noe JM, Arndt KA, et al. Port-wine stains: morphologic variations and developmental lesions. Arch Dermatol 1984;120: 1453-1455
22. Smoller BS, Rosen S. Port-wine stain: a disease of altered neural modulation of blood vessels? Arch Dermatol 1986;122:177-179
23. Rydh M, Malm M, Jernbeck J, et al. Ectatic blood vessels in port wine stains lack innervation: possible role in pathogenesis. Plast Reconstr Surg 1991;87:419-422
24. Del Pozo J, Pazos JM, Fonseca E. Lower lip hypertrophy secondary to port-wine stain: combined surgical and carbon dioxide laser treatment. Dermatol Surg 2004;30:211-214
25. Sanchez-Carpintero I, Mihm MC, Mizeracki A, et al. Epithelial and mesenchymal hamartomatous changes in a mature port-wine stain: morphologic evidence for a multiple germ layer field defect. J Am Acad Dermatol 2004;50:608-612
26. Yukna RA, Cassingham RJ, Carr RF. Periodontal manifestations and treatment in a case of Sturge-Weber syndrome. Oral Surg 1979;47: 408-415
27. Ramli N, Sachet M, Bao C, et al. Cerebrofacial venous metameric syndrome (CVMS) 3: Sturge-Weber syndrome with bilateral lymphatic/ venous malformations of the mandible. Neuroradiology 2003;45: 687-690
28. Lin DDM, Gailloud P, McCarthy EF, et al. Oromaxillofacial osseous abnormality in Sturge-Weber syndrome: case report and review of the literature. Am J Neuroradiol 2006;27:274-277
29. Mulliken JB. Capillary (Port-Wine) and other telangiectatic stains. In: Mulliken JB, Young AE. Vascular Birthmarks: Hemangiomas and Malformations. Philadelphia, PA: WB. Saunders; 1988:178