CLINICAL IMAGE |
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Year : 2018 | Volume
: 11
| Issue : 2 | Page : 166-168 |
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Von Hipple–Lindau: Unusual case presentation with peripheral and juxtapapillary retinal hemangioma
Kanika Jain, Manav Deep Singh
Department of Ophthalmology, Dr. RML Hospital, New Delhi, India
Correspondence Address:
Kanika Jain S-293, Ground Floor, Greater Gailash 1, New Delhi - 110 048 India
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/ojo.OJO_30_2017
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Von Hipple-Lindua (VHL) syndrome is an autosomal dominant neoplastic disorder in which multiple benign or malignant tumours and cysts develop in central nervous system and visceral organs. Retinal capillary hemangioma is the most frequent and often the earliest manifestation of VHL syndrome. We report a case with multisystemic involvement diagnosed as a case of multiple endocrine neoplasia (MEN) syndrome but the presence of multiple, unilateral peripheral and juxtapapillary retinal capillary hemangioma was able to clinche the definative diagnosis of VHL and thus helped in appropriate management of the patient.
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