stapedial artery
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2021 ◽  
Vol 71 (Suppl-3) ◽  
pp. S491-94
Author(s):  
Muhammad Atif Najam ◽  
Urwa Sarwar ◽  
Maqbool Raza ◽  
Khalid Azam Khan ◽  
Humaira Saleem ◽  
...  

Objective: To assess the hearing results of transcanal endoscopic stapedotomy Study Design: Descriptive study. Place and Duration of Study: Pakistan Naval Ship Hafeez Islamabad Pakistan, from Jun 2016 to Jun 2020. Methodology: All patients with surgically confirmed otosclerosis were included in the study. All patients were operated with 0-degree 3mm, 14cm rigid endoscope under general anesthesia. Preoperative and post operative air bone gap was noted along with demographic data, middle ear anomalies (persistent stapedial artery, dehiscent facial nerve, anteriorly placed facial nerve, floating foot plate) and injury to chorda tympani. Postoperative air bone gap (A-B Gap) was documented 12 weeks after surgery. All patients were followed up for 6-12 months Results: Mean age of patients was, 37 years and standard deviation was 12.34 (range 27-52 years). Out of total 45 cases 13 were males (29%) and 32 females (71.%). Four (8.8%) patients had dehiscent facial canal and 1 (2.2%) patient had persistent stapedial artery. Average preoperative A-B gap was 35 db and Average Postoperative A-B Gap was 7 db. Chorda tympani was preserved in all cases. One patient (2.2%) complained of altered taste which resolved after 3 months. Four patients had Postoperative vertigo that lasted 2 days on average. Conclusion: Endoscopic trans canal Stapes surgery is scarless safe effective procedure demonstrable hearing benefits in all patients with minimum complications. The Technique is single handed and has steep learning curve.


2021 ◽  
pp. 014556132110320
Author(s):  
Collin J. O’Bryan ◽  
James J. Klemens

A persistent stapedial artery is a congenital vascular malformation that can cause tinnitus and/or conductive hearing loss. Although rare, this case highlights the importance of recognizing aberrant anatomy as a potential cause of patients’ symptoms. It also demonstrates how to recognize and treat patients with a symptomatic persistent stapedial artery.


2020 ◽  
Vol 42 (1) ◽  
pp. 160-166
Author(s):  
Z.J. LoVerde ◽  
D.P. Shlapak ◽  
J.C. Benson ◽  
M.L. Carlson ◽  
J.I. Lane

2020 ◽  
Vol 41 (6) ◽  
pp. 102684
Author(s):  
Pedrom C. Sioshansi ◽  
Amy E. Schettino ◽  
Seilesh C. Babu ◽  
Dennis I. Bojrab ◽  
Elias M. Michaelides ◽  
...  

2020 ◽  
Vol 16 (3) ◽  
pp. 463-466
Author(s):  
T. Logan Lindemann ◽  
◽  
Katie L. Austin ◽  
Arun K. Gadre ◽  
◽  
...  

2020 ◽  
Vol 41 (10) ◽  
pp. 1768-1776
Author(s):  
S. Bonasia ◽  
S. Smajda ◽  
G. Ciccio ◽  
T. Robert
Keyword(s):  

2020 ◽  
Vol 26 (5) ◽  
pp. 675-680
Author(s):  
Federico Cagnazzo ◽  
Riccardo Zannoni ◽  
Pierre-Henri Lefevre ◽  
Cyril Dargazanli ◽  
Imad Derraz ◽  
...  

The stapedial artery (SA) is an embryonic vessel connecting the internal carotid artery (ICA) to the branches of the future external carotid artery (ECA). It passes through the primordium of the stapes that progressively develops around the SA. Normally, SA disappears during the tenth week in utero. Approximately 0.4% of the population can have a persistent SA. It can persist as four types of embryological variations, of which the pharyngo-hyo-stapedial variant has been rarely described before. We reported a case of a 61-year-old woman presented with transient ischemic attacks (TIAs). Computed tomography angiography showed an unusual “duplicated” aspect of the left ICA. Digital subtraction angiography depicted a persistent pharyngo-hyo-stapedial artery with an atherosclerotic wall and was considered the cause of the TIAs. After failure of the antiplatelet therapy in preventing recurrent TIAs, stenting of the artery was planned and successfully performed. Patient was asymptomatic during 12-month follow-up. The pharyngo-hyo-stapedial artery is a very rare variation in which the SA is supplied by the inferior tympanic (rising from the ascending pharyngeal artery) and the hyoid artery (rising from the ICA). To our knowledge, this is a unique case of a pharyngo-hyo-stapedial artery in a patient presenting associated ischemic symptoms. Radiological and embryological findings are discussed.


2020 ◽  
Vol 16 (2) ◽  
pp. 274-277
Author(s):  
Mélanie Sanjuan ◽  
◽  
Frédérique Chapon ◽  
Jacques Magnan ◽  
◽  
...  
Keyword(s):  

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