scholarly journals Idiopathic Spontaneous Intraperitoneal Hemorrhage due to Rupture of Short Gastric Artery Presenting as Massive Gastrointestinal Bleeding: A Rare Case Presentation and Literature Review

Cureus ◽  
2020 ◽  
Author(s):  
Yasir Saeed ◽  
Zahava Farkas ◽  
Sulaiman Azeez
Keyword(s):  
Literature Review ◽  
Gastrointestinal Bleeding ◽  
Rare Case ◽  
Gastric Artery ◽  
Case Presentation ◽  
Intraperitoneal Hemorrhage ◽  
Massive Gastrointestinal Bleeding

scholarly journals Duplication of Inferior Vena Cava, Possible Cause of Internal Hernia? Literature Review and Rare Case Presentation

Chirurgia ◽  
2020 ◽  
Vol 115 (5) ◽  
pp. 665
Author(s):  
Cedric Kwizera ◽  
Daniel G. Popa ◽  
Marian Botoncea ◽  
Adrian Tudor ◽  
Gyorgy D. Szava ◽  
...  
Keyword(s):  
Literature Review ◽  
Inferior Vena Cava ◽  
Internal Hernia ◽  
Rare Case ◽  
Inferior Vena ◽  
Vena Cava ◽  
Case Presentation ◽  
Possible Cause

Duodenal Perforation with Transplant Hepatic Artery Pseudo-Aneurysm: A Rare Case of Massive Gastrointestinal Bleeding

2018 ◽  
Vol 113 (Supplement) ◽  
pp. S1286
Author(s):  
RajaKoteswar Dhanekula ◽  
Kaitlyn Votta ◽  
Adam M. Frank ◽  
Ashesh P. Shah ◽  
David A. Sass
Keyword(s):  
Gastrointestinal Bleeding ◽  
Hepatic Artery ◽  
Rare Case ◽  
Duodenal Perforation ◽  
Massive Gastrointestinal Bleeding ◽  
Pseudo Aneurysm

scholarly journals Intratracheal myiasis followed by tracheal-esophageal fistula: report of a rare case and literature review

2019 ◽  
Vol 19 (1) ◽  
Author(s):  
Wendi Huang ◽  
Chao Zeng ◽  
Weidong Song ◽  
Ping Xu
Keyword(s):  
Literature Review ◽  
Clinical Features ◽  
Male Patient ◽  
Stent Placement ◽  
Rare Case ◽  
Healthcare Providers ◽  
Living Environment ◽  
Esophageal Fistula ◽  
Case Presentation ◽  
History Of

Abstract Background To enhance awareness of the clinical features and prevention of endotracheal myiasis. Case presentation A case of intratracheal myiasis is reported. A 61-year-old male patient with a history of laryngectomy was admitted to hospital due to tracheostomal hemorrhage of 3 h duration. Intratracheal myiasis was confirmed by bronchoscopy, and the patient underwent bronchoscopic intervention, which was complicated by a tracheal-esophageal fistula and resolved by endotracheal stenting. Twenty months after stent placement, the fistula had not healed. Conclusion Intratracheal myiasis has serious complications and is difficult to treat. For post-tracheostomy patients, healthcare providers and caregivers should pay attention to the care and monitoring of wounds and maintenance of a tidy, clean living environment to prevent intratracheal myiasis.

Massive gastrointestinal bleeding due to rectovaginal fistula: A rare case report

2021 ◽  
pp. 1-3
Author(s):  
Şehmus ÖLMEZ ◽  
Sevda BAŞ ◽  
Nevin AKÇAER ÖZTÜRK ◽  
Okan DİLEK ◽  
Bünyamin SARITAŞ
Keyword(s):  
Case Report ◽  
Gastrointestinal Bleeding ◽  
Rectovaginal Fistula ◽  
Rare Case ◽  
Massive Gastrointestinal Bleeding ◽  
Rare Case Report

scholarly journals RARE-52. SACRAL LIPOMATOSIS OF THE NERVE: A RARE CASE PRESENTATION AND LITERATURE REVIEW

2016 ◽  
Vol 18 (suppl_6) ◽  
pp. vi170-vi170
Author(s):  
Juanita Garces ◽  
Mansour Mathkour ◽  
Joshua Hanna ◽  
Cuong J. Bui ◽  
Olawale A.R. Sulaiman
Keyword(s):  
Literature Review ◽  
Rare Case ◽  
Case Presentation

Fatal Case of Vulvar Pyoderma Gangrenosum with Pulmonary Involvement: Case Presentation and Literature Review

2014 ◽  
Vol 18 (6) ◽  
pp. 424-429 ◽  
Author(s):  
Joshua M. Mercer ◽  
Paul Kuzel ◽  
Muhammad N. Mahmood ◽  
Alain Brassard
Keyword(s):  
Literature Review ◽  
Pyoderma Gangrenosum ◽  
Rare Case ◽  
Fatal Case ◽  
Pulmonary Involvement ◽  
Review Of The Literature ◽  
Treatment Resistant ◽  
Case Presentation ◽  
First Case ◽  
Systemic Therapies

Introduction: We report a case of a 61-year-old woman with locally destructive vulvar pyoderma gangrenosum (PG) with pulmonary involvement who was refractory to numerous systemic therapies and developed complications resulting in her demise. Objective: To report a rare case of treatment-resistant vulvar PG with pulmonary involvement that proved to be fatal. Methods: PubMed was used to search for other reports that discuss PG, or more specifically perigenital PG, with pulmonary involvement. Results and Conclusion: A thorough review of the literature revealed 33 cases of PG with pulmonary involvement, with only 4 involving the perigenital region. We report the second case of a female with vulvar PG and pulmonary involvement. In contrast to the first case described, our patient did not respond to systemic therapy, and, ultimately, her disease was fatal. It is hoped that with continued documentation of this rare and potentially lethal presentation of PG, physicians will determine more effective treatments.

A rare cause of hydronephrosis: Leiomyoma of the ureter and a literature review

2021 ◽  
pp. 039156032110104
Author(s):  
Furkan Umut Kilic ◽  
Uygar Micoogullari ◽  
Serkan Altinova
Keyword(s):  
Back Pain ◽  
Literature Review ◽  
Rare Case ◽  
Partial Cystectomy ◽  
Differential Diagnoses ◽  
Genitourinary Tract ◽  
Case Presentation ◽  
The Right ◽  
Distal Ureterectomy

Introduction: Leiomyomas of the genitourinary tract are rare and their manifestation in the ureter is even rarer. To our knowledge, only 14 cases of leiomyoma of the ureter have been reported worldwide since 1955, therefore this case will be 15th. Case presentation: We present a rare case of primary leiomyoma of the right ureter. Ureteroscopy did not show any abnormal findings in the ureteral mucosa. The primary leiomyoma was resected with distal ureterectomy and partial cystectomy that was followed with ureteroneocystostomy due to extraluminal mass that caused hydronephrosis and back pain. Conclusion: Although rare, we believe that leiomyoma should be considered in the differential diagnoses of well-circumscribed ureteral masses and kidney-sparing surgery should be performed.

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