Endolymphatic Sac Tumor: A Rare Case
Endolymphatic Sac Tumor: A Rare Case
Download Citation in txt
Download Citation in bib
Download Citation in ris
Author Info
Amal Algarni Yaser Orz Sofia Muzzafar Wafa Alshakweer
Corresponding Author
Amal AlgarniPathology Resident, Pathology and Clinical Pathology Administration, King Fahad Medical City, Riyadh, Saudi Arabia
A B S T R A C T
Endolymphatic sac tumor is rare, locally aggressive and non-metastasizing neoplasm arising from the endolymphatic sac of the petrous portion of the temporal bone. Most occur in adult and present with ipsilateral hearing loss. They can be sporadic or associated with Von-Hippel-Lindau disease. Patient with endolymphatic sac tumor should be screened for VHL disease. We report a case of 52-year-old female with dizziness and headache. Histopathology was consistent with typical features of endolymphatic sac tumor. This was confirmed by cytokeratin and EMA positivity and TTF-1 negativity. This case is presented for its rarity with only few cases reported.
Article Info
Article Type
Case ReportPublication history
Received: Tue 07, Jul 2020Accepted: Thu 16, Jul 2020
Published: Mon 31, Aug 2020
Copyright
© 2023 Amal Algarni. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Hosting by Science Repository.DOI: 10.31487/j.JSO.2020.04.04