Endolymphatic sac tumor: Difference between revisions

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<gallery>
File:Post_contrast_T1_weighted_MRI_demonstrates_intense_enhancement_of_both_the_eye_and_the_endolymphatic_sac_tumor..jpg|Post contrast T1 weighted MRI demonstrates intense enhancement of both the eye and the endolymphatic sac tumor.
File:CT_through_the_petrous_ridge_ELST_VHL.jpg|CT through the petrous ridge showing endolymphatic sac tumor in Von Hippel-Lindau disease.
File:Ear_Endolymphatic_Sac_Tumor_H_and_E_Low_power_LDRT.tif|Ear Endolymphatic Sac Tumor H and E Low power.
File:Ear_Endolymphatic_Sac_Tumor_H_&_E_High_power_LDRT.tif|Ear Endolymphatic Sac Tumor H & E High power.
</gallery>

Latest revision as of 11:28, 18 February 2025

Endolymphatic Sac Tumor is a rare, slow-growing tumor that originates in the endolymphatic sac, a part of the inner ear. These tumors are associated with Von Hippel-Lindau disease, a genetic condition that causes tumors and cysts to grow in the body.

Symptoms[edit]

The symptoms of an endolymphatic sac tumor can vary, but often include:

Diagnosis[edit]

Diagnosis of an endolymphatic sac tumor typically involves a combination of medical history, physical examination, and imaging tests such as MRI or CT scan.

Treatment[edit]

Treatment options for endolymphatic sac tumors include:

Prognosis[edit]

The prognosis for individuals with an endolymphatic sac tumor varies depending on the size and location of the tumor, as well as the individual's overall health.

See Also[edit]

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