CC BY-NC-ND 4.0 · Asian J Neurosurg 2016; 11(03): 311
DOI: 10.4103/1793-5482.179644
CASE REPORT

Cerebellospinal hemangioblastoma with bilateral pheochromocytoma and hepatic cyst: A rare entity

Mrinal Bhuyan
Department of Neurosurgery, Gauhati Medical College, Guwahati, Assam
,
Deep Dutta
Department of Neurosurgery, Gauhati Medical College, Guwahati, Assam
,
Basanta Baishya
Department of Neurosurgery, Gauhati Medical College, Guwahati, Assam
,
Zakir Hussain
Department of Neurosurgery, Gauhati Medical College, Guwahati, Assam
› Author Affiliations

A 45-year-old gentleman presented with headache, dizziness, and unsteadiness of gait. On imaging, he was found to have a cerebellar and a spinal intramedullary hemangioblastoma. To rule out Von Hippel–Lindau (VHL) disease, we did screening of the whole abdomen with ultrasonography followed by contrast-enhanced computed tomography of the abdomen, and surprisingly, the patient was having bilateral adrenal pheochromocytoma and a hepatic cyst. A diagnosis of VHL disease was made on this basis. The patient was operated and he made a very good recovery. We are reporting this interesting case because of its typical findings and its rarity. Disease management and review of literature were also discussed at the end.



Publication History

Article published online:
20 September 2022

© 2016. Asian Congress of Neurological Surgeons. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)

Thieme Medical and Scientific Publishers Pvt. Ltd.
A-12, 2nd Floor, Sector 2, Noida-201301 UP, India