PRESS

Dental Crown Aspiration

Siavash Kooranifar; Samira Nakhaei*

    The patient is a 45 year-old female who works as a hospital personnel (secretary) with no significant medical history. She had sudden cardiac arrest while she was at work. Chest compression was commenced immediately. She underwent endotracheal intubation and electrical defibrillation was successful. After 3 days she was extubated and admitted to intensive care unit, but she had dry cough. Computed tomography of chest revealed a radiopaque foreign body in the right lower lobe bronchus and bilateral alveolar infiltration...


Pneumopericardium: A Case Report

Ibrahima Sory Sylla*; Mamadou Aliou Baldé; Sana Samoura; Souleymane Diakité; Bah Mamadou Bassirou; Alpha Koné; Ibrahima Sory Barry; Maraime Béavogui; Djibril Sylla; Elhadj Yaya Baldé; Mamadi Condé; Mamadou Dadhi Baldé

    Pneumopericardium is defined as the presence of air within the pericardial space. Usually, it is a complication of blunt or penetrating chest trauma, but rare iatrogenic and spontaneous cases have been reported [1]. We report the case of a 21-year old girl admitted to the emergency department for road traffic injury with a favourable outcome.


Dyspnea in a 26-Year-Old Woman with Fatal Left Atrial Myxoma

Ibrahima Sory Sylla*; Mamadou Aliou Baldé; Mamadou Bassirou Bah; Sana Samoura; Souleymane Diakité; Alpha Koné; Ibrahima Sory Barry; Maraime Béavogui; Djibril Sylla; Elhadj Yaya Baldé; Mamadi Condé; Mamadou Dadhi Baldé

    Cardiac myxoma is one of the primary intracardiac tumours. We report the case of a left atrial myxoma in a 26-year-old female patient admitted for investigation of dyspnoea. Echocardiography led to the diagnosis of a giant hypermobile myxoma prolapsing into the left ventricle. The patient died before being evacuated for surgical treatment.


A 42-Year-Old Man with a Solitary Kidney

Fredrick Kalokola*; Deodatus Mabula; Benard Gombanila; Ladius Rudovick; Said Kanenda

    It is estimated that 1/2000 people have a solitary kidney and they are at risk for developing arterial hypertension and impaired renal function. Hypertension is an independent risk factor for progression of renal disease in people born with a solitary kidney. Early detection, regular follow up and prompt management of blood pressure may help slow the progression of renal function impairment.


Sinus Node Dysfunction in People Who Have Down Syndrome with Structurally Normal Hearts: A Case Series

Verity Chadwick; Caroline Medi; Mark McGuire; Ali Sepahpour; Paolo D’Ambrosio; David S Celermajer; Rachael Cordina*

    Down Syndrome (DS) is the most common chromosomal abnormality in live born infants. Although limited research suggests that autonomic dysfunction may be more common in the setting of DS, a predisposition to cardiac conduction abnormalities is not well recognised. We performed a retrospective review of records at our tertiary referral centre from Jan 2018 to Jan 2021 to identify people who had Down’s syndrome and required permanent pacemaker implantation for cardiac conduction disease.


Sudden Cardiac Arrest Following Sexual Activity in an Asymptomatic Patient with Undiagnosed Hypertrophic Cardiomyopathy: A Case Report

Annie Berg*; Jigish Khamar; Nathan How; Bennett Haynen

    Background: The American Heart Association (AHA) guidelines suggest that sexual activity is reasonable for most patients with Hypertrophic Cardiomyopathy (HCM) however, it should be deferred for patients with severe symptoms until clinically stabilized. Furthermore, the AHA scientific committee noted that no Sudden Cardiac Arrest (SCA) cases linked to sexual activity in HCM have been documented. Therefore, this case report describes


Persistent Left Superior Vena Cava, a Challenge for Pacemaker Implantation: One Case Report

A Maliki Alaoui*; F El Hassan; O Sidati; F Chikhi; I Fellat; M Cherti

    Persistent left superior vena cava is a rare congenital malformation, usually without clinical impact, due to the persistence of the anterior cardinal vein. It is detected in approximately 3% of autopsies and in 2% to 4% of patients with congenital heart disease.


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