PT  - JOURNAL ARTICLE
AU  - Lin, D.D.M.
AU  - Gailloud, P.
AU  - McCarthy, E.F.
AU  - Comi, A.M.
TI  - Oromaxillofacial Osseous Abnormality in Sturge-Weber Syndrome: Case Report and Review of the Literature
DP  - 2006 Feb 01
TA  - American Journal of Neuroradiology
PG  - 274--277
VI  - 27
IP  - 2
4099  - http://www.ajnr.org/content/27/2/274.short
4100  - http://www.ajnr.org/content/27/2/274.full
SO  - Am. J. Neuroradiol.2006 Feb 01; 27
AB  - SUMMARY: We report a case of a 17-month-old child affected by Sturge-Weber syndrome who had unusually rapid overgrowth of the left frontal, temporal, orbital, and maxillary regions. CT angiography illustrated osteohypertrophy with periostitis and associated soft tissue hypertrophy directly corresponding to the distribution of the cutaneous port-wine stain. Extended maxillectomy was performed because of rapid growth and clinical debilitation, with surgical pathology revealing juvenile ossifying fibroma.