Otic polyp: Difference between revisions

Content deleted Content added
SDPatrolBot (talk | contribs)
Replace template requesting speedy deletion under A3 removed by page creator) (bot edit
m Fix 1 auth/ed/transl punctuation; WP:GenFixes on
 
(22 intermediate revisions by 14 users not shown)
Line 1:
{{Infobox medical condition (new)
{{Db-a3}}
| name =
An otic polyp (also called [[aural]] polyp) is a benign proliferation of chronic inflammatory cells associated with [[granulation tissue]], in response to a longstanding inflammatory process of the [[middle ear]].
| synonyms = Aural polyp
<ref name="Nair">{{Cite pmid|15165306}}</ref>
| image = Ear Otic Polyp H&E LDRT.tif
<ref name="Prasannaraj">{{Cite pmid|12761701}}</ref>
| alt =
<ref name="Hussain">{{Cite pmid|7543918}}</ref>
| caption = An intermediate magnification of a H&E stained biopsy from an otic polyp.
<ref name="Gliklich">{{Cite pmid|8499099}}</ref>
| pronounce =
<ref name="Kurihara">{{Cite pmid|1746847}}</ref>
| field = [[ENT surgery]]
<ref name="Friedmann">{{cite pmid|2406442}}</ref>
| symptoms =
| complications =
| onset =
| duration =
| types =
| causes =
| risks =
| diagnosis =
| differential =
| prevention =
| treatment =
| medication =
| prognosis =
| frequency =
| deaths =
}}
 
An '''otic polyp''' is a benign proliferation of chronic inflammatory cells associated with [[granulation tissue]], in response to a longstanding inflammatory process of the [[middle ear]].<ref name="Prasannaraj">{{Cite journal | last1 = Prasannaraj | first1 = T. | last2 = De | first2 = N. S. | last3 = Narasimhan | first3 = I. | title = Aural polyps: Safe or unsafe disease? | journal = American Journal of Otolaryngology | volume = 24 | issue = 3 | pages = 155–158 | year = 2003 | pmid = 12761701 | doi=10.1016/s0196-0709(02)32426-8}}</ref><ref name="Gliklich">{{Cite journal | last1 = Gliklich | first1 = R. E. | last2 = Cunningham | first2 = M. J. | last3 = Eavey | first3 = R. D. | title = The cause of aural polyps in children | journal = Archives of Otolaryngology–Head & Neck Surgery | volume = 119 | issue = 6 | pages = 669–671 | year = 1993 | pmid = 8499099 | doi=10.1001/archotol.1993.01880180089016}}</ref>
 
== Signs and symptoms ==
Patients usually present with [[otorrhea]], conductive [[hearing loss]], and [[otalgia]], while bleeding and a sensation of a mass are much less common.<ref name="Gliklich"/>
 
<ref name="Nair">{{Cite pmid|15165306}}</ref>
==Diagnosis==
<ref name="Prasannaraj">{{Cite pmid|12761701}}</ref>
=== Imaging findings ===
<ref name="Hussain">{{Cite pmid|7543918}}</ref>
<ref name="Gliklich">{{Cite pmid|8499099}}</ref>
<ref name="Kurihara">{{Cite pmid|1746847}}</ref>
<ref name="Friedmann">{{cite pmid|2406442}}</ref>
== Imaging findings ==
Although imaging is not required to yield a diagnosis, it may be obtained to exclude other disorders, such as a concurrent [[cholesteatoma]].
 
=== Pathology findings ===
By gross description, there is usually a solitary, polypoid, reddish mass behind an intact ear drum (typmanictympanic membrane). The tissue is often friable, measuring <2 &nbsp;cm in most cases. All tissue should be processed in order to exclude a concurrent cholesteatoma.<ref name="Friedmann">{{Cite journal | last1 = Friedmann | first1 = I. | title = Pathological lesions of the external auditory meatus: A review | journal = Journal of the Royal Society of Medicine | volume = 83 | issue = 1 | pages = 34–37 | year = 1990 | pmid = 2406442 | pmc = 1292463| doi = 10.1177/014107689008300115 }}</ref>
[[File:Ear_Otic_Polyp_H&E_LDRT.tif|thumb|Descripton.]]
 
By gross description, there is usually a solitary, polypoid, reddish mass behind an intact ear drum (typmanic membrane). The tissue is often friable, measuring <2 cm in most cases. All tissue should be processed in order to exclude a concurrent cholesteatoma.
By microscopic exam, the polypoid appearance is maintained, showing a granulation-type tissue reaction with edematous stroma and a rich investment by capillaries. The surface of the polyp is covered by stratified squamous epitehliumepithelium with a prominent granular cell layer. The tissue is filled with lymphocytes, plasma cells, mast cells, histiocytes, and eosinophils. It is not uncommon to see plasma cells with Russell bodies and Mott cell formation. Depending on length of symptoms, multinucleated giant cells and calcifications may be seen. Other disorders may be concurrently present, especially since this is a post infectious/inflammatory disorder, and these include a cholesterol granuloma, "tunnel clusters" (glandular epithelial inclusions below the surface epithelium), and [[cholesteatoma]].<ref name="Friedmann"/><ref name="Nair">{{Cite journal | last1 = Nair | first1 = S. | last2 = Watts | first2 = S. | last3 = Flood | first3 = L. | doi = 10.1258/002221504323086507 | title = Fibroblast growth factor receptor expression in aural polyps: Predictor of cholesteatoma? | journal = The Journal of Laryngology & Otology | volume = 118 | issue = 5 | pages = 338–342 | year = 2006 | pmid = 15165306 }}</ref><ref name="Hussain">{{Cite journal | last1 = Hussain | first1 = S. S. | last2 = Hopkinson | first2 = J. M. | title = Mast cells in aural polyps: A preliminary report | journal = The Journal of Laryngology and Otology | volume = 109 | issue = 6 | pages = 491–494 | year = 1995 | pmid = 7543918 | doi=10.1017/s0022215100130543}}</ref>
 
By microscopic exam, the polypoid appearance is maintained, showing a granulation-type tissue reaction with edematous stroma and a rich investment by capillaries. The surface of the polyp is covered by stratified squamous epitehlium with a prominent granular cell layer. The tissue is filled with lymphocytes, plasma cells, histiocytes, and eosinophils. It is not uncommon to see plasma cells with Russell bodies and Mott cell formation. Depending on length of symptoms, multinucleated giant cells and calcifications may be seen. Other disorders may be concurrently present, especially since this is a post infectious/inflammatory disorder, and these include a cholesterol granuloma, "tunnel clusters" (glandular epithelial inclusions below the surface epithelium), and cholesteatoma.
<ref name="Nair">{{Cite pmid|15165306}}</ref>
<ref name="Prasannaraj">{{Cite pmid|12761701}}</ref>
<ref name="Hussain">{{Cite pmid|7543918}}</ref>
<ref name="Gliklich">{{Cite pmid|8499099}}</ref>
<ref name="Kurihara">{{Cite pmid|1746847}}</ref>
<ref name="Friedmann">{{cite pmid|2406442}}</ref>
=== Immunohistochemistry ===
[[Immunohistochemistry]] is unnecessary for the diagnosis, but will highlight a mixed B- and T-cell population within the lymphoid component, without light chain (kappa or lambda) restriction. Any muscle markers would be negative.
 
<ref name="Nair">{{Cite pmid|15165306}}</ref>
=== Differential diagnoses ===
<ref name="Prasannaraj">{{Cite pmid|12761701}}</ref>
The lesion presents in young patients, so the differential for a "polyp", especially when the lymphoid component is crushed or dominant, would include a [[rhabdomyosarcoma]], [[extramedullary plasmacytoma]], and a [[Neuroendocrine adenoma middle ear|neuroendocrine adenoma of the middle ear]].
<ref name="Hussain">{{Cite pmid|7543918}}</ref>
 
<ref name="Gliklich">{{Cite pmid|8499099}}</ref>
<ref name="Kurihara">{{Cite pmid|1746847}}</ref>
<ref name="Friedmann">{{cite pmid|2406442}}</ref>
== Differential diagnoses ==
The lesion presents in young patients, so the differential for a "polyp", especially when the lymphoid component is crushed or dominant, would include a [[rhabdomyosarcoma]], [[extramedullary plasmacytoma]], and a neuroendocrine adenoma of the middle ear.
== Management ==
Since this lesion is usually a complication of long standing otitis media, it is important to use an appropriate antibiotic therapy regimen. If the patient fails first line antibiotics, then second-line therapies should be employed, especially after appropriate culture and sensitivity testing. Surgery may be required if there is extension into the mastoid bone, or if a concurrent cholesteatoma is identified during surgery or biopsy. In general, patients have an excellent outcome after appropriate therapy. <ref name="NairPrasannaraj"/>{{Cite pmid|15165306}}<ref name="Gliklich"/><ref name="Friedmann"/>
 
<ref name="Prasannaraj">{{Cite pmid|12761701}}</ref>
<ref name="Hussain">{{Cite pmid|7543918}}</ref>
<ref name="Gliklich">{{Cite pmid|8499099}}</ref>
<ref name="Kurihara">{{Cite pmid|1746847}}</ref>
<ref name="Friedmann">{{cite pmid|2406442}}</ref>
== Epidemiology ==
This is an uncommon lesion, usually affecting young patients (mean age, 30 years), with a male to female ratio of 2:1. The middle ear is involved, although it may extend to the external auditory canal if there is tympanic membrane perforation.<ref name="Prasannaraj"/><ref name="Gliklich"/><ref name="Friedmann"/>
<ref name="Nair">{{Cite pmid|15165306}}</ref>
 
<ref name="Prasannaraj">{{Cite pmid|12761701}}</ref>
<ref name="Hussain">{{Cite pmid|7543918}}</ref>
<ref name="Gliklich">{{Cite pmid|8499099}}</ref>
<ref name="Kurihara">{{Cite pmid|1746847}}</ref>
<ref name="Friedmann">{{cite pmid|2406442}}</ref>
== References ==
{{Reflist}}
 
== Further reading ==
{{cite book |authorauthor1=Lester D. R. Thompson, |author2=Bruce M. Wenig |title=Diagnostic Pathology: Head and Neck: Published by Amirsys |publisher=Lippincott Williams & Wilkins |location=Hagerstown, MD |year=2011 |pages=7:16-1716–17 |isbn=978-1-931884-61-7 |oclc= |doi= |accessdate=}}
 
== External links ==
{{Medical resources
| DiseasesDB =
| ICD10 =
| ICD9 =
| ICDO =
| OMIM =
| MedlinePlus = 001638
| eMedicineSubj =
| eMedicineTopic =
| MeSH =
| GeneReviewsNBK =
| GeneReviewsName =
}}
 
[[Category:Ear]]