FACIAL VASCULAR MALFORMATION IN A CASE OF NEUROFIBROMATOSIS TYPE 1 - A RARE ASSOCIATION

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Published: 2016-01-02

Page: 151-154


RUCHIRA DAS *

Department of Radiology, IPGMER and SSKM Hospital, 242, A.J.C Bose Road, Kolkata-700020, India

SAMIR SONAR

Department of Radiology, IPGMER and SSKM Hospital, 242, A.J.C Bose Road, Kolkata-700020, India

ARCHANA SINGH

Department of Radiology, IPGMER and SSKM Hospital, 242, A.J.C Bose Road, Kolkata-700020, India

NILANJAN PANDA

Department of Radiology, IPGMER and SSKM Hospital, 242, A.J.C Bose Road, Kolkata-700020, India

*Author to whom correspondence should be addressed.


Abstract

Neurofibromatosis type 1 is a phakomatosis associated with many neoplasms and malformations. Although common manifestations include multiple café au lait macules, benign neurofibromas, iris hamartomas and skeletal abnormalities, it is rarely associated with vascular lesions like stenosis, aneurysms and arteriovenous malformations. This case presentation shows a rare association of facial arteriovenous malformation with neurofibromatosis type 1 in a child.

Keywords: Neurofibromatosis type 1, facial arteriovenous malformation, NF-1 vasculopathy, FASI


How to Cite

DAS, R., SONAR, S., SINGH, A., & PANDA, N. (2016). FACIAL VASCULAR MALFORMATION IN A CASE OF NEUROFIBROMATOSIS TYPE 1 - A RARE ASSOCIATION. Journal of Disease and Global Health, 6(4), 151–154. Retrieved from https://ikprress.org/index.php/JODAGH/article/view/1933

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