Journal of Clinical and Diagnostic Research, ISSN - 0973 - 709X

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Case report
Year : 2017 | Month : October | Volume : 11 | Issue : 10 | Page : PD07 - PD09

Supratentorial Haemangioblastoma without Von Hippel-Lindau Disease A Rare Case Report with Review of Literature

Salman Tehran Shaikh, Chandrashekhar Eknath Deopujari

1. Neurosurgery Resident, Department of Neurosurgery, Bombay Hospital Institute of Medical Sciences, Mumbai, Maharashtra, India. 2. Head, Department of Neurosurgery, Bombay Hospital Institute of Medical Sciences, Mumbai, Maharashtra, India.

Correspondence Address :
Dr. Salman Tehran Shaikh,
V-1, Row House II, Sector-6, Vashi, Navi Mumbai-400703, Maharashtra, India.


Haemangioblastomas are slow-growing, benign and vascular neoplasms of the central nervous system. They are usually infratentorial, occurring either sporadically in approximately 67% of cases or as a manifestation of Von Hippel-Lindau (VHL) disease in approximately 33% of cases. They were first described by Von Hippel in 1895. Haemangioblastoma in the supratentorial compartment is an infrequent occurrence. Only 58 cases of supratentorial haemangioblastoma without Von Hippel-Lindau disease have been reported from 1902 to 2015. This case discusses a left basifrontal supratentorial haemangioblastoma occurring in a young female who presented with headache and blurring of vision without manifestations of VHL disease. Its benign nature and prognosis merited surgical excision as the treatment of choice.


Haemangioblastoma, Supratentorial, Von hippel-lindau disease

How to cite this article :

Salman Tehran Shaikh, Chandrashekhar Eknath Deopujari. SUPRATENTORIAL HAEMANGIOBLASTOMA WITHOUT VON HIPPEL-LINDAU DISEASE A RARE CASE REPORT WITH REVIEW OF LITERATURE. Journal of Clinical and Diagnostic Research [serial online] 2017 October [cited: 2018 Jan 17 ]; 11:PD07-PD09. Available from

DOI and Others

DOI: 10.7860/JCDR/2017/29520.10767

Date of Submission: Apr 14, 2017
Date of Peer Review: Aug 03, 2017
Date of Acceptance: Sep 15, 2017
Date of Publishing: Oct 01, 2017


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