Warthin's tumor natural history, complications and prognosis: Difference between revisions
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==Prognosis== | ==Prognosis== | ||
* The long-term outlook for people with Warthin tumor is generally good. | * The long-term outlook for people with Warthin tumor is generally good. | ||
* The tumor is almost always benign and is generally cured with surgery. | * The [[tumor]] is almost always [[benign]] and is generally [[Cure|cured]] with surgery. | ||
* The risk of recurrence | * The risk of recurrence is thought to be 2% or less.<ref>Warthin tumor. Genetic and Rare Diseases Information Center (GARD) (2015). https://rarediseases.info.nih.gov/gard/8569/warthin-tumor/resources/1 Accessed on December 14, 2015</ref> | ||
==References== | ==References== | ||
{{reflist|2}} | {{reflist|2}} | ||
Revision as of 19:24, 3 December 2018
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Warthin's tumor Microchapters |
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Diagnosis |
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Treatment |
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Case Studies |
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Warthin's tumor natural history, complications and prognosis On the Web |
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American Roentgen Ray Society Images of Warthin's tumor natural history, complications and prognosis |
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FDA on Warthin's tumor natural history, complications and prognosis |
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CDC on Warthin's tumor natural history, complications and prognosis |
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Warthin's tumor natural history, complications and prognosis in the news |
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Blogs on Warthin's tumor natural history, complications and prognosis |
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Risk calculators and risk factors for Warthin's tumor natural history, complications and prognosis |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Ammu Susheela, M.D. [2]
Overview
If left untreated, few patients with Warthin's tumor may progress to develop facial paralysis. Common complications of Warthin's tumor include squamous cell carcinoma and facial paralysis. Prognosis is generally good.
Natural History
- If left untreated, few patients with Warthin's tumor may progress to develop facial paralysis.
Complications
Prognosis
- The long-term outlook for people with Warthin tumor is generally good.
- The tumor is almost always benign and is generally cured with surgery.
- The risk of recurrence is thought to be 2% or less.[1]
References
- ↑ Warthin tumor. Genetic and Rare Diseases Information Center (GARD) (2015). https://rarediseases.info.nih.gov/gard/8569/warthin-tumor/resources/1 Accessed on December 14, 2015