Cargando…
A Rare Case of Endolymphatic Sac Tumour: Clinicopathologic Study and Surgical Management
Objective. Endolymphatic sac tumor (ELST) is a rare neoplasm arising from the intrapetrous portion of the endolymphatic sac, either isolated or in association with the von Hippel-Lindau disease. We report a sporadic case of ELST with an overview of the literature and a discussion of clinic-radiologi...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4065704/ https://www.ncbi.nlm.nih.gov/pubmed/24991442 http://dx.doi.org/10.1155/2014/376761 |
_version_ | 1782322128266199040 |
---|---|
author | Ferri, Emanuele Amadori, Maurizio Armato, Enrico Pavon, Ida |
author_facet | Ferri, Emanuele Amadori, Maurizio Armato, Enrico Pavon, Ida |
author_sort | Ferri, Emanuele |
collection | PubMed |
description | Objective. Endolymphatic sac tumor (ELST) is a rare neoplasm arising from the intrapetrous portion of the endolymphatic sac, either isolated or in association with the von Hippel-Lindau disease. We report a sporadic case of ELST with an overview of the literature and a discussion of clinic-radiological, histopathologic, and surgical findings. Case Report. A young woman presented with a progressive hearing loss in the left ear. Otoscopy showed a reddish, bleeding hypotympanic mass. CT demonstrated an expansile lytic mastoid lesion extending to the middle ear, with bone erosion. MRI confirmed a lesion of increased signal on T1-weighted sequences. The patient underwent a canal wall-down tympanoplasty with complete removal of the tumor. Histopathology was consistent with a papillary ELST. Immunohistochemistry was positive for cytokeratin and chromogranin A. Conclusion. This paper highlights the rarity of ELST, the need for an accurate neuroradiological and immunohistochemical study at the early stages, and the timeliness of surgical treatment. |
format | Online Article Text |
id | pubmed-4065704 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-40657042014-07-02 A Rare Case of Endolymphatic Sac Tumour: Clinicopathologic Study and Surgical Management Ferri, Emanuele Amadori, Maurizio Armato, Enrico Pavon, Ida Case Rep Otolaryngol Case Report Objective. Endolymphatic sac tumor (ELST) is a rare neoplasm arising from the intrapetrous portion of the endolymphatic sac, either isolated or in association with the von Hippel-Lindau disease. We report a sporadic case of ELST with an overview of the literature and a discussion of clinic-radiological, histopathologic, and surgical findings. Case Report. A young woman presented with a progressive hearing loss in the left ear. Otoscopy showed a reddish, bleeding hypotympanic mass. CT demonstrated an expansile lytic mastoid lesion extending to the middle ear, with bone erosion. MRI confirmed a lesion of increased signal on T1-weighted sequences. The patient underwent a canal wall-down tympanoplasty with complete removal of the tumor. Histopathology was consistent with a papillary ELST. Immunohistochemistry was positive for cytokeratin and chromogranin A. Conclusion. This paper highlights the rarity of ELST, the need for an accurate neuroradiological and immunohistochemical study at the early stages, and the timeliness of surgical treatment. Hindawi Publishing Corporation 2014 2014-06-04 /pmc/articles/PMC4065704/ /pubmed/24991442 http://dx.doi.org/10.1155/2014/376761 Text en Copyright © 2014 Emanuele Ferri et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Ferri, Emanuele Amadori, Maurizio Armato, Enrico Pavon, Ida A Rare Case of Endolymphatic Sac Tumour: Clinicopathologic Study and Surgical Management |
title | A Rare Case of Endolymphatic Sac Tumour: Clinicopathologic Study and Surgical Management |
title_full | A Rare Case of Endolymphatic Sac Tumour: Clinicopathologic Study and Surgical Management |
title_fullStr | A Rare Case of Endolymphatic Sac Tumour: Clinicopathologic Study and Surgical Management |
title_full_unstemmed | A Rare Case of Endolymphatic Sac Tumour: Clinicopathologic Study and Surgical Management |
title_short | A Rare Case of Endolymphatic Sac Tumour: Clinicopathologic Study and Surgical Management |
title_sort | rare case of endolymphatic sac tumour: clinicopathologic study and surgical management |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4065704/ https://www.ncbi.nlm.nih.gov/pubmed/24991442 http://dx.doi.org/10.1155/2014/376761 |
work_keys_str_mv | AT ferriemanuele ararecaseofendolymphaticsactumourclinicopathologicstudyandsurgicalmanagement AT amadorimaurizio ararecaseofendolymphaticsactumourclinicopathologicstudyandsurgicalmanagement AT armatoenrico ararecaseofendolymphaticsactumourclinicopathologicstudyandsurgicalmanagement AT pavonida ararecaseofendolymphaticsactumourclinicopathologicstudyandsurgicalmanagement AT ferriemanuele rarecaseofendolymphaticsactumourclinicopathologicstudyandsurgicalmanagement AT amadorimaurizio rarecaseofendolymphaticsactumourclinicopathologicstudyandsurgicalmanagement AT armatoenrico rarecaseofendolymphaticsactumourclinicopathologicstudyandsurgicalmanagement AT pavonida rarecaseofendolymphaticsactumourclinicopathologicstudyandsurgicalmanagement |