| CASE REPORT |
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| Year : 2021 | Volume
: 11
| Issue : 1 | Page : 44-46 |
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Encephalotrigeminal angiomatosis with facial lobular capillary hemangioma: An unusual case report
Amol Karagir1, Shridevi Adaki1, Dilip Magdum2
1 Department of Oral Medicine and Radiology, BVDU Dental College, Sangli, Maharashtra, India
2 Department of Oral and Maxillofacial Pathology, BVDU Dental College, Sangli, Maharashtra, India
Correspondence Address:
Shridevi Adaki
Department of Oral Medicine and Radiology, BVDU Dental College, Sangli - 416 414, Maharashtra
India
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/ijabmr.IJABMR_301_19
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Encephalotrigeminal angiomatosis, also called Sturge–Weber syndrome (SWS), is a syndrome of etiology which is not yet clear. It is a nonhereditary condition. The clinical features include pigmentation over the facial skin known as port-wine stain, abnormalities of ocular region, and central nervous system involvement as leptomeningeal angioma. In this manuscript, we present a rare case report with an unusual combination of SWS with facial lobular capillary hemangioma.
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