Loading…
Persistent Stapedial Artery, Oval Window Atresia and Congenital Stapes Agenesis-Case Report
: The persistent stapedial artery (PSA) is a rare congenital vascular malformation involving the middle ear. It is usually associated with pulsatile tinnitus and/or conductive hearing loss and can account for multiple risks during middle ear surgery. : we present a case of a 9-year-old male child wi...
Saved in:
Published in: | Medicina (Kaunas, Lithuania) Lithuania), 2023-02, Vol.59 (3), p.461 |
---|---|
Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c525t-392f13b3cba72adb3d05863b9dfc4954409adf1be8943274ed3e5fb5f2221b443 |
---|---|
cites | cdi_FETCH-LOGICAL-c525t-392f13b3cba72adb3d05863b9dfc4954409adf1be8943274ed3e5fb5f2221b443 |
container_end_page | |
container_issue | 3 |
container_start_page | 461 |
container_title | Medicina (Kaunas, Lithuania) |
container_volume | 59 |
creator | Gheorghe, Dan Cristian Epure, Veronica Oprea, Doru Zamfir-Chiru-Anton, Adina |
description | : The persistent stapedial artery (PSA) is a rare congenital vascular malformation involving the middle ear. It is usually associated with pulsatile tinnitus and/or conductive hearing loss and can account for multiple risks during middle ear surgery.
: we present a case of a 9-year-old male child with conductive hearing loss and persistent stapedial artery in his right ear, who was admitted to our ENT Department for hearing loss. During surgery, we discovered PSA along with congenital stapes agenesis and oval window atresia, as well as an abnormal trajectory of the mastoid segment of the facial nerve. After ossicular reconstruction (transcanal total ossicular replacement prosthesis) with cochleostomy, no surgical complications were recorded and hearing improvement was monitored by pre- and postoperative audiometry.
: Stapedial artery is a rare anatomical middle ear abnormality that can prevent proper surgical hearing restoration and can be associated with other simultaneous temporal bone malformations. |
doi_str_mv | 10.3390/medicina59030461 |
format | article |
fullrecord | <record><control><sourceid>gale_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_4d094b80008848379ee8c0fd5540e1fb</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A743767393</galeid><doaj_id>oai_doaj_org_article_4d094b80008848379ee8c0fd5540e1fb</doaj_id><sourcerecordid>A743767393</sourcerecordid><originalsourceid>FETCH-LOGICAL-c525t-392f13b3cba72adb3d05863b9dfc4954409adf1be8943274ed3e5fb5f2221b443</originalsourceid><addsrcrecordid>eNptkttrFDEUxgdRbK2--yQDvjr15DYzeZJh8VIoVLzggw8hk5ysWXaTNclW-t-bdmvtiuQhOZfvx8nHaZrnBE4Zk_B6g9YbH7SQwID35EFzTHo-dpJw_vDe-6h5kvMKgFEx0MfNEevlyHlPj5vvHzFlnwuG0n4ueluBet1OqWC6etVeXNbgmw82_mqnkjB73epg20UMSwy-1OqNKLdTjWs5dwudsf2E25jK0-aR0-uMz27vk-bru7dfFh-684v3Z4vpvDOCitIxSR1hMzOzHqi2M7Mgxp7N0jrDpeAcpLaOzDhKzujA0TIUbhaOUkpmztlJc7bn2qhXapv8RqcrFbVXN4mYlkqn4s0aFbcg-TwCwDjykQ0ScTTgrBAckLi5st7sWdvdXN011Zek1wfQw0rwP9QyXioCIGQvr6d5eUtI8ecOc1GruEuhGqDoIEk_gCDwt2up61g-uFhpZuOzUdPA2dAPTLLadfqfrnosbryJAZ2v-QMB7AUmxZwTurvJCajrlVH_rkyVvLj_4zvBnx1hvwH4k70e</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2791670510</pqid></control><display><type>article</type><title>Persistent Stapedial Artery, Oval Window Atresia and Congenital Stapes Agenesis-Case Report</title><source>Publicly Available Content Database</source><source>PubMed Central(OpenAccess)</source><creator>Gheorghe, Dan Cristian ; Epure, Veronica ; Oprea, Doru ; Zamfir-Chiru-Anton, Adina</creator><creatorcontrib>Gheorghe, Dan Cristian ; Epure, Veronica ; Oprea, Doru ; Zamfir-Chiru-Anton, Adina</creatorcontrib><description>: The persistent stapedial artery (PSA) is a rare congenital vascular malformation involving the middle ear. It is usually associated with pulsatile tinnitus and/or conductive hearing loss and can account for multiple risks during middle ear surgery.
: we present a case of a 9-year-old male child with conductive hearing loss and persistent stapedial artery in his right ear, who was admitted to our ENT Department for hearing loss. During surgery, we discovered PSA along with congenital stapes agenesis and oval window atresia, as well as an abnormal trajectory of the mastoid segment of the facial nerve. After ossicular reconstruction (transcanal total ossicular replacement prosthesis) with cochleostomy, no surgical complications were recorded and hearing improvement was monitored by pre- and postoperative audiometry.
: Stapedial artery is a rare anatomical middle ear abnormality that can prevent proper surgical hearing restoration and can be associated with other simultaneous temporal bone malformations.</description><identifier>ISSN: 1648-9144</identifier><identifier>ISSN: 1010-660X</identifier><identifier>EISSN: 1648-9144</identifier><identifier>DOI: 10.3390/medicina59030461</identifier><identifier>PMID: 36984462</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Abnormalities ; Agenesis ; Arteries - abnormalities ; Carotid arteries ; Case Report ; Case reports ; Causes of ; Child ; cochleostomy ; Complications and side effects ; Diagnosis ; Ear, Middle - abnormalities ; Ear, Middle - surgery ; Hearing loss ; Hearing Loss, Conductive - etiology ; Hearing Loss, Conductive - surgery ; Heart ; Humans ; Male ; Medical imaging ; Ossicular Prosthesis ; ossiculoplasty ; Otolaryngology ; Pediatric research ; persistent stapedial artery ; Prostheses ; Stapes - abnormalities ; Stapes - blood supply ; Surgery ; Tinnitus ; Veins & arteries</subject><ispartof>Medicina (Kaunas, Lithuania), 2023-02, Vol.59 (3), p.461</ispartof><rights>COPYRIGHT 2023 MDPI AG</rights><rights>2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2023 by the authors. 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c525t-392f13b3cba72adb3d05863b9dfc4954409adf1be8943274ed3e5fb5f2221b443</citedby><cites>FETCH-LOGICAL-c525t-392f13b3cba72adb3d05863b9dfc4954409adf1be8943274ed3e5fb5f2221b443</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2791670510/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2791670510?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25732,27903,27904,36991,44569,53770,53772,74873</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36984462$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gheorghe, Dan Cristian</creatorcontrib><creatorcontrib>Epure, Veronica</creatorcontrib><creatorcontrib>Oprea, Doru</creatorcontrib><creatorcontrib>Zamfir-Chiru-Anton, Adina</creatorcontrib><title>Persistent Stapedial Artery, Oval Window Atresia and Congenital Stapes Agenesis-Case Report</title><title>Medicina (Kaunas, Lithuania)</title><addtitle>Medicina (Kaunas)</addtitle><description>: The persistent stapedial artery (PSA) is a rare congenital vascular malformation involving the middle ear. It is usually associated with pulsatile tinnitus and/or conductive hearing loss and can account for multiple risks during middle ear surgery.
: we present a case of a 9-year-old male child with conductive hearing loss and persistent stapedial artery in his right ear, who was admitted to our ENT Department for hearing loss. During surgery, we discovered PSA along with congenital stapes agenesis and oval window atresia, as well as an abnormal trajectory of the mastoid segment of the facial nerve. After ossicular reconstruction (transcanal total ossicular replacement prosthesis) with cochleostomy, no surgical complications were recorded and hearing improvement was monitored by pre- and postoperative audiometry.
: Stapedial artery is a rare anatomical middle ear abnormality that can prevent proper surgical hearing restoration and can be associated with other simultaneous temporal bone malformations.</description><subject>Abnormalities</subject><subject>Agenesis</subject><subject>Arteries - abnormalities</subject><subject>Carotid arteries</subject><subject>Case Report</subject><subject>Case reports</subject><subject>Causes of</subject><subject>Child</subject><subject>cochleostomy</subject><subject>Complications and side effects</subject><subject>Diagnosis</subject><subject>Ear, Middle - abnormalities</subject><subject>Ear, Middle - surgery</subject><subject>Hearing loss</subject><subject>Hearing Loss, Conductive - etiology</subject><subject>Hearing Loss, Conductive - surgery</subject><subject>Heart</subject><subject>Humans</subject><subject>Male</subject><subject>Medical imaging</subject><subject>Ossicular Prosthesis</subject><subject>ossiculoplasty</subject><subject>Otolaryngology</subject><subject>Pediatric research</subject><subject>persistent stapedial artery</subject><subject>Prostheses</subject><subject>Stapes - abnormalities</subject><subject>Stapes - blood supply</subject><subject>Surgery</subject><subject>Tinnitus</subject><subject>Veins & arteries</subject><issn>1648-9144</issn><issn>1010-660X</issn><issn>1648-9144</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkttrFDEUxgdRbK2--yQDvjr15DYzeZJh8VIoVLzggw8hk5ysWXaTNclW-t-bdmvtiuQhOZfvx8nHaZrnBE4Zk_B6g9YbH7SQwID35EFzTHo-dpJw_vDe-6h5kvMKgFEx0MfNEevlyHlPj5vvHzFlnwuG0n4ueluBet1OqWC6etVeXNbgmw82_mqnkjB73epg20UMSwy-1OqNKLdTjWs5dwudsf2E25jK0-aR0-uMz27vk-bru7dfFh-684v3Z4vpvDOCitIxSR1hMzOzHqi2M7Mgxp7N0jrDpeAcpLaOzDhKzujA0TIUbhaOUkpmztlJc7bn2qhXapv8RqcrFbVXN4mYlkqn4s0aFbcg-TwCwDjykQ0ScTTgrBAckLi5st7sWdvdXN011Zek1wfQw0rwP9QyXioCIGQvr6d5eUtI8ecOc1GruEuhGqDoIEk_gCDwt2up61g-uFhpZuOzUdPA2dAPTLLadfqfrnosbryJAZ2v-QMB7AUmxZwTurvJCajrlVH_rkyVvLj_4zvBnx1hvwH4k70e</recordid><startdate>20230225</startdate><enddate>20230225</enddate><creator>Gheorghe, Dan Cristian</creator><creator>Epure, Veronica</creator><creator>Oprea, Doru</creator><creator>Zamfir-Chiru-Anton, Adina</creator><general>MDPI AG</general><general>MDPI</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20230225</creationdate><title>Persistent Stapedial Artery, Oval Window Atresia and Congenital Stapes Agenesis-Case Report</title><author>Gheorghe, Dan Cristian ; Epure, Veronica ; Oprea, Doru ; Zamfir-Chiru-Anton, Adina</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c525t-392f13b3cba72adb3d05863b9dfc4954409adf1be8943274ed3e5fb5f2221b443</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Abnormalities</topic><topic>Agenesis</topic><topic>Arteries - abnormalities</topic><topic>Carotid arteries</topic><topic>Case Report</topic><topic>Case reports</topic><topic>Causes of</topic><topic>Child</topic><topic>cochleostomy</topic><topic>Complications and side effects</topic><topic>Diagnosis</topic><topic>Ear, Middle - abnormalities</topic><topic>Ear, Middle - surgery</topic><topic>Hearing loss</topic><topic>Hearing Loss, Conductive - etiology</topic><topic>Hearing Loss, Conductive - surgery</topic><topic>Heart</topic><topic>Humans</topic><topic>Male</topic><topic>Medical imaging</topic><topic>Ossicular Prosthesis</topic><topic>ossiculoplasty</topic><topic>Otolaryngology</topic><topic>Pediatric research</topic><topic>persistent stapedial artery</topic><topic>Prostheses</topic><topic>Stapes - abnormalities</topic><topic>Stapes - blood supply</topic><topic>Surgery</topic><topic>Tinnitus</topic><topic>Veins & arteries</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gheorghe, Dan Cristian</creatorcontrib><creatorcontrib>Epure, Veronica</creatorcontrib><creatorcontrib>Oprea, Doru</creatorcontrib><creatorcontrib>Zamfir-Chiru-Anton, Adina</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health Medical collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Medicina (Kaunas, Lithuania)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gheorghe, Dan Cristian</au><au>Epure, Veronica</au><au>Oprea, Doru</au><au>Zamfir-Chiru-Anton, Adina</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Persistent Stapedial Artery, Oval Window Atresia and Congenital Stapes Agenesis-Case Report</atitle><jtitle>Medicina (Kaunas, Lithuania)</jtitle><addtitle>Medicina (Kaunas)</addtitle><date>2023-02-25</date><risdate>2023</risdate><volume>59</volume><issue>3</issue><spage>461</spage><pages>461-</pages><issn>1648-9144</issn><issn>1010-660X</issn><eissn>1648-9144</eissn><abstract>: The persistent stapedial artery (PSA) is a rare congenital vascular malformation involving the middle ear. It is usually associated with pulsatile tinnitus and/or conductive hearing loss and can account for multiple risks during middle ear surgery.
: we present a case of a 9-year-old male child with conductive hearing loss and persistent stapedial artery in his right ear, who was admitted to our ENT Department for hearing loss. During surgery, we discovered PSA along with congenital stapes agenesis and oval window atresia, as well as an abnormal trajectory of the mastoid segment of the facial nerve. After ossicular reconstruction (transcanal total ossicular replacement prosthesis) with cochleostomy, no surgical complications were recorded and hearing improvement was monitored by pre- and postoperative audiometry.
: Stapedial artery is a rare anatomical middle ear abnormality that can prevent proper surgical hearing restoration and can be associated with other simultaneous temporal bone malformations.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>36984462</pmid><doi>10.3390/medicina59030461</doi><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1648-9144 |
ispartof | Medicina (Kaunas, Lithuania), 2023-02, Vol.59 (3), p.461 |
issn | 1648-9144 1010-660X 1648-9144 |
language | eng |
recordid | cdi_doaj_primary_oai_doaj_org_article_4d094b80008848379ee8c0fd5540e1fb |
source | Publicly Available Content Database; PubMed Central(OpenAccess) |
subjects | Abnormalities Agenesis Arteries - abnormalities Carotid arteries Case Report Case reports Causes of Child cochleostomy Complications and side effects Diagnosis Ear, Middle - abnormalities Ear, Middle - surgery Hearing loss Hearing Loss, Conductive - etiology Hearing Loss, Conductive - surgery Heart Humans Male Medical imaging Ossicular Prosthesis ossiculoplasty Otolaryngology Pediatric research persistent stapedial artery Prostheses Stapes - abnormalities Stapes - blood supply Surgery Tinnitus Veins & arteries |
title | Persistent Stapedial Artery, Oval Window Atresia and Congenital Stapes Agenesis-Case Report |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-22T07%3A32%3A11IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Persistent%20Stapedial%20Artery,%20Oval%20Window%20Atresia%20and%20Congenital%20Stapes%20Agenesis-Case%20Report&rft.jtitle=Medicina%20(Kaunas,%20Lithuania)&rft.au=Gheorghe,%20Dan%20Cristian&rft.date=2023-02-25&rft.volume=59&rft.issue=3&rft.spage=461&rft.pages=461-&rft.issn=1648-9144&rft.eissn=1648-9144&rft_id=info:doi/10.3390/medicina59030461&rft_dat=%3Cgale_doaj_%3EA743767393%3C/gale_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c525t-392f13b3cba72adb3d05863b9dfc4954409adf1be8943274ed3e5fb5f2221b443%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2791670510&rft_id=info:pmid/36984462&rft_galeid=A743767393&rfr_iscdi=true |