scholarly journals Type IA urethral duplication: a case report

2019 ◽  
Vol 8 (3) ◽  
pp. 767
Author(s):  
Miftah Adityagama ◽  
Yonas Immanuel Hutasoit
Keyword(s):  
Case Report ◽  
Urethral Duplication ◽  
Type Ia

Zenith AAA endovascular graft suprarenal bare metal stent separation with graft migration and type IA endoleak

Vascular ◽  
2021 ◽  
pp. 170853812110627
Author(s):  
Julian Smith ◽  
Simon Joseph ◽  
Catherine Thoo
Keyword(s):  
Case Report ◽  
Endovascular Repair ◽  
Bare Metal Stent ◽  
Main Body ◽  
Bare Metal ◽  
Metal Stent ◽  
Endovascular Graft ◽  
Abdominal Aortic ◽  
Type Ia ◽  
Graft Migration

Background The Zenith endovascular graft (Cook Medical, Bloomington, IN, USA) is a well-recognised device used in endovascular repair of abdominal aortic aneurysms (EVAR). After a small number of reported cases of suprarenal stent separation from the main body of the graft, modifications were made to the strength and durability of the suture line attachment of the proximal bare metal component prior to release in 2003. This report describes a further case of suprarenal stent separation and type IA endoleak in a patient who underwent an EVAR using the Zenith device in 2012. Methods We present a case report of a 77-year-old male with incidental finding of type IA endoleak on a background of elective endovascular repair for 50.4-mm infrarenal abdominal aortic aneurysm (AAA), with a Cook Zenith endograft. Computed tomography (CT) demonstrated separation of the suprarenal bare metal stent from the main body of the endograft, with resultant graft migration and increase in native aneurysm sac size. Results The patient underwent semi-urgent surgery with successful placement of a bridging thoracic stent graft between the lowest renal artery and main body of the pre-existing graft. Conclusions This case report describes a rare complication of Zenith devices, additionally emphasising the importance of regular surveillance imaging following EVAR.

scholarly journals Rare presentation of incomplete male urethral duplication: A case report and review of literature

2021 ◽  
Vol 9 (1) ◽  
pp. 292-296
Author(s):  
Orgeness J Mbwambo ◽  
Alex Mremi ◽  
Mohamed Mbarouk ◽  
Jasper Mbwambo ◽  
Frank Bright ◽  
...  
Keyword(s):  
Congenital Anomaly ◽  
Case Report ◽  
Postoperative Period ◽  
Surgical Removal ◽  
Urethral Duplication ◽  
Review Of Literature ◽  
Rare Presentation ◽  
Rare Congenital Anomaly ◽  
Accessory Urethra

Urethral duplication is a rare congenital anomaly affecting mainly males. Here, we report a case of urethral duplication in a 19 years old male presented as a scrotal sinus discharging pus for 1 year. Surgical removal of accessory urethra was done and postoperative period was uneventful.

scholarly journals Congenital duplication of the urethra with urethral diverticulum: a case report

F1000Research ◽  
2014 ◽  
Vol 3 ◽  
pp. 99 ◽  
Author(s):  
Darshan H Shah ◽  
Arvind P Ganpule ◽  
Ravindra B Sabnis ◽  
Mahesh R Desai
Keyword(s):  
Congenital Anomaly ◽  
Case Report ◽  
Treatment Modality ◽  
List Item ◽  
Urethral Diverticulum ◽  
Endoscopic Management ◽  
List Type ◽  
Urethral Duplication ◽  
Small Opening ◽  
Rare Congenital Anomaly

Duplication of the urethra is a rare congenital anomaly. Urethral duplication with the presence of diverticulum is a rare combination and to the best of our knowledge has  not been previously reported. We report a case of a 16 month old male child with duplication of the urethra and diverticulum arising from the ventral urethra. We also cover the intricacies and challenges in the management of such a case.The opening of the narrowed accessory dorsal urethra at the verumontanum was cauterized and gradually the dorsal urethra became atrophied. The ventral urethral diverticulum was excised. This case is unique due to:The unusual presentation of swelling over the dorsum of the penis, together with duplication of the urethra with diverticulum.The use of cauterization as a treatment modality. Cauterization of the ventral urethra with a Bugbee electrode and diverticulectomy was performed. A glidewire helped in identifying the small opening of the dorsal urethra at the level of the verumontanum. The case also highlights the importance of endoscopic management of this clinical entity.

Urethral duplication in a 1 year old: a rare case report

2021 ◽  
Vol 14 (5) ◽  
pp. e240844
Author(s):  
Deepak Vineel Sai Kallepalli ◽  
Prakash Agarwal ◽  
Jegadeesh Sundaram ◽  
Selvapriya Bharathi
Keyword(s):  
Urinary Tract Infection ◽  
Case Report ◽  
Rare Case ◽  
Classification Systems ◽  
Urethral Duplication ◽  
Associated Anomalies ◽  
Urethrocutaneous Fistula ◽  
Recurrent Uti ◽  
Rare Case Report ◽  
Accessory Urethra

An 8-month-old male child presented with the complaint of two separate urinary streams from the penis. The child had no complaints of incontinence or recurrent UTI (urinary tract infection). Initial diagnosis of urethrocutaneous fistula was made and proceeded to micturating cystourethrography (MCU) and found to be having a urethral duplication. The duplicated urethra was excised and accessory urethra closed. Postoperatively, the child was followed up for 1 year and had no complaints of recurrence or incontinence. Through this case report, we learn about different classification systems and types of urethral duplication and their associated anomalies, and mode of management, which is mainly surgical. Further, management should be individualised to each patient based on their complaints and intraoperative findings.

scholarly journals Minor Papillary Relief in a Type IA Choledochal Cyst: A Case Report and Review of the Literature

2020 ◽  
Vol 14 (1) ◽  
pp. 116-123
Author(s):  
Sindhura Kolli ◽  
Simcha Weissman ◽  
Emmanuel Ofori ◽  
Khoi Paul Dang-Ho ◽  
Praneeth Bandaru ◽  
...  
Keyword(s):  
Case Report ◽  
Choledochal Cyst ◽  
Classification System ◽  
Lag Time ◽  
Diagnosis And Treatment ◽  
Review Of The Literature ◽  
Choledochal Cysts ◽  
Diagnosis And Management ◽  
System Diagnosis ◽  
Type Ia

Choledochal cysts are an anatomical conundrum as they present with nonspecific symptoms generally delaying diagnosis and treatment. Its lag time remains critical, as cholangiocarcinoma, a fatal sequelae, contributes to its morbidity and mortality. Herein, we present a case of a type 1A choledochal cyst. We hope that its review on presentation, classification system, diagnosis, and management prevent complications and cataclysmic results.

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