Simultaneously occurring Zenker's diverticulum and Killian–Jamieson diverticulum: case report and literature review

2017 ◽  
Vol 131 (8) ◽  
pp. 661-666 ◽  
Author(s):  
K E Stewart ◽  
D R K Smith ◽  
S L Woolley

AbstractBackground:Pharyngoesophageal diverticula have many subtypes, with Zenker's diverticulum being the most common. First described in 1983, a Killian–Jamieson diverticulum is an outpouching in the anterolateral wall at the pharyngoesophageal junction. This is located inferiorly to the cricopharyngeus muscle, unlike Zenker's diverticula which occur superiorly. Killian–Jamieson diverticula are rare and are commonly misdiagnosed as Zenker's diverticula. Less than 30 reports of Killian–Jamieson diverticula have been described in the literature.Case report:A 69-year-old man presented with a 2-year symptomatic history, and was found to have simultaneous Zenker's diverticulum and Killian–Jamieson diverticulum. He was treated successfully with open surgical excision of both pouches.Conclusion:Zenker's diverticulum and Killian–Jamieson diverticulum are diagnosed using radiological studies and endoscopy. Their differentiation is important, as surgical management differs. This paper reviews the literature on Killian–Jamieson diverticula and the management options available.

2010 ◽  
Vol 124 (10) ◽  
pp. 1129-1131 ◽  
Author(s):  
T Klockars ◽  
A Mäkitie

AbstractObjective:We report identical twins with Zenker's diverticulum.Methods:Case report and literature review.Conclusions:Geographical and racial variation in occurrence, and rare familial cases, suggest that inherited factors play a role in the pathogenesis of Zenker's diverticulum. The identical twins reported here provide further evidence supporting a genetic predisposition.


Author(s):  
Moawia Elbalal ◽  
Abu Baker Mohamed ◽  
Anas Hamdoun ◽  
Khalid Yassin ◽  
Elhadi Miskeen ◽  
...  

Author(s):  
Jun Arima ◽  
Sang-Woong Lee ◽  
Kohei Taniguchi ◽  
Sadakatsu Senpuku ◽  
Tetsunosuke Shimizu ◽  
...  

A linear stapler was used to reduce the leakage rate during a Zenker’s diverticulum diverticulectomy. However, staple line reinforcement was not used, and leakage occurred. The efficacy of staple line reinforcement in the literature was unclear; however, reinforcement may be necessary for Zenker’s diverticulum cases.


2010 ◽  
Vol 24 (3) ◽  
pp. 173-174 ◽  
Author(s):  
René D Boisvert ◽  
Drew CG Bethune ◽  
David Acton ◽  
Denis R Klassen

A Killian-Jamieson diverticulum is an outpouching from the lateral wall of the proximal cervical esophagus. These diverticula are rare and are distinct from the more commonly known Zenker’s diverticulum. Literature regarding Killian-Jamieson diverticula and its suggested management is scarce. The present report describes a patient with symptomatic bilateral Killian-Jamieson diverticula. The patient had both diverticula excised and an esophagomyotomy performed. Following surgery, the patient’s symptoms resolved and he recovered well. A literature review and discussion of the etiology, clinical presentation and radiographic findings of Killian-Jamieson diverticulum follow, as do recommendations for clinical management.


2017 ◽  
Vol 68 (3) ◽  
pp. 240-244
Author(s):  
Sumiyo Saburi ◽  
Yoichiro Sugiyama ◽  
Hideki Bando ◽  
Ryuichi Hirota ◽  
Yasuo Hisa ◽  
...  

2020 ◽  
Vol 02 ◽  
Author(s):  
Masood Ghori ◽  
Nadya O. Al Matrooshi ◽  
Samir Al Jabbari ◽  
Ahmed Bafadel ◽  
Gopal Bhatnagar

: Infective Endocarditis (IE), a known complication of hemodialysis (HD), has recently been categorized as Healthcare-Associated Infective Endocarditis (HAIE). Single pathogen bacteremia is common, polymicrobial endocardial infection is rare in this cohort of the patients. We report a case of endocarditis caused by Enterococcus faecalis (E. faecalis) and Burkholderia cepacia (B. cepacia), a first ever reported combination of a usual and an unusual organism, respectively, in a patient on HD. Clinical presentation of the patient, its complicated course ,medical and surgical management ,along with microbial and echocardiographic findings is presented herein. The authors believe that presentation of this case of HAIE may benefit and contribute positively to cardiac science owing to the rare encounter of this organism as a pathogen in infective endocarditis and the difficulties in treating it.


Medicina ◽  
2021 ◽  
Vol 57 (5) ◽  
pp. 483
Author(s):  
Brîndușa Cimpoca ◽  
Amira Moldoveanu ◽  
Nicolae Gică ◽  
Corina Gică ◽  
Anca Marina Ciobanu ◽  
...  

Heterotopic pregnancy is the condition where both intrauterine and ectopic pregnancy are present. It rarely occurs after natural conception, but is more common with assisted reproductive techniques, when more than one embryo is transferred. Quadruplet heterotopic pregnancy is exceedingly rare. Methods: A literature review was conducted aiming to highlight the diagnosis difficulties and the management options in heterotopic quadruplet pregnancies. Results: Nine relevant studies were identified by researching PubMed up to 2021 for “heterotopic quadruplet pregnancy”, “quadruplet intrauterine and ectopic pregnancy”, “synchronous intrauterine and ectopic pregnancy”. Conclusions: In this paper, we present a case of heterotopic quadruplet pregnancy and address the difficulty in diagnosing this condition and make formal recommendations.


1984 ◽  
Vol 37 (3) ◽  
pp. 189-191 ◽  
Author(s):  
Biing-shiun Huang ◽  
W. Spencer Payne ◽  
Alan J. Cameron

2012 ◽  
Vol 6 (4) ◽  
pp. 449-466 ◽  
Author(s):  
Ivana Dzeletovic ◽  
Dale C Ekbom ◽  
Todd H Baron

2021 ◽  
Author(s):  
Amala Sunder ◽  
bessy Varghese ◽  
noora bahzad ◽  
basma darwish

Abstract Aim: The study is the Case Report of spontaneous parasitic myoma with omental vessel, and the management at Bahrain Defense Force Hospital. Case Report: A 35years old female was diagnosed, almost 20 cm, sub serous myoma with the pedicle of 2cm from the fundus of the uterus. There was a feeding vessel from the omentum. She underwent myomectomy after the resection of pedicle and omental vessel .Post-operative period was uneventful. Conclusion: Parasitic myoma is the type of subserous uterine myoma. Generally surgical management is required for the relief of symptoms and to avoid encroachment of nearby abdominal or pelvic structures which in turn leads to further complications.


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