 
								Case Report: A Rare Case of Coronary-Bronchial Fistula Associated with a Large Lung Bullae and Bronchiectasis Presenting as Dyspnea
								
									
										
											
											
												Farid Maalouf,
											
										
											
											
												Nadine Kawkabani,
											
										
											
											
												Simon Bejjani,
											
										
											
											
												Omar Boustros,
											
										
											
											
												Nabil Khoury,
											
										
											
											
												Abbas Chamsuddin,
											
										
											
											
												Rola Darwish,
											
										
											
											
												Pierrette Habib,
											
										
											
											
												Bassam Abou Khalil,
											
										
											
											
												Paul Charbel
											
										
									
								 
								
									
										Issue:
										Volume 5, Issue 3, May 2019
									
									
										Pages:
										56-59
									
								 
								
									Received:
										29 May 2019
									
									Accepted:
										29 June 2019
									
									Published:
										11 July 2019
									
								 
								
								
								
									
									
										Abstract: Coronary artery fistulas (CAF) are rare but hemodynamically significant anomalies. Although asymptomatic, they can be associated with several cardiorespiratory conditions. Coronary to bronchial fistulas (CBF) account for 0.5% to 0.61% of coronary artery fistulas, with fistulas arising from the right coronary artery being exceedingly rare. These fistulas are known to be associated with bronchiectasis but not lung bullae. The following paper reports a rare case of a coronary to bronchial fistula associated to bronchiectasis and lung bullae. The patient presented for dyspnea and was found to have a large lung bullae, bronchiectasis and a coronary to bronchial artery fistula arising from the right coronary artery and terminating into the left bronchial artery. The CBF was successfully managed first with percutaneous microcoil embolization then the bullae was resected thoracoscopically three days later. However, more case reports are mandatory in order to further understand the etiology and pathophysiology of these fistulas, elucidate their relationship to other pathologies such as bronchiectasis and lung bullae and determine the optimal therapeutic measures.
										Abstract: Coronary artery fistulas (CAF) are rare but hemodynamically significant anomalies. Although asymptomatic, they can be associated with several cardiorespiratory conditions. Coronary to bronchial fistulas (CBF) account for 0.5% to 0.61% of coronary artery fistulas, with fistulas arising from the right coronary artery being exceedingly rare. These fis...
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								Atrial Septal Defect with Rheumatic Mitral Regurgitation: A Rare Association in a Nigerian Child
								
									
										
											
											
												Olugbenga Olalekan Ojo,
											
										
											
											
												Uvie Ufuoma Onakpoya,
											
										
											
											
												John Akintunde Okeniyi,
											
										
											
											
												Anthony Taiwo Adenekan,
											
										
											
											
												Muyiwa Afolabi Owojuyigbe,
											
										
											
											
												Oluwakemi Tolu Adegoke
											
										
									
								 
								
									
										Issue:
										Volume 5, Issue 3, May 2019
									
									
										Pages:
										60-63
									
								 
								
									Received:
										12 August 2019
									
									Accepted:
										3 September 2019
									
									Published:
										18 September 2019
									
								 
								
								
								
									
									
										Abstract: Atrial septal defect (ASD) coexisting with mitral valve regurgitation has been described in literature with various aetiologies and pathophysiologic mechanisms. Mitral valve lesions coexisting with an ASD could either be congenital or acquired. The most prominent congenital mitral valve pathology is a cleft in the anterior leaflet of the mitral valve, as seen in patients with partial atrio-ventricular septal defects. Acquired mitral valve lesions include, hemodynamic induced annular dilatation resulting in significant mitral regurgitation, iatrogenic leaflet perforation and coexisting diseases such as infective endocarditis or rheumatic valve disease. However, the aetiology of the mitral valve regurgitation being due to rheumatic heart disease is uncommon. We report the case of a 12-year-old female who presented with easy fatigability, palpitation and a precordial bulge dating about 2 years. Examination revealed cardiac murmurs in the apex and pulmonary areas and transthoracic echocardiography confirmed the presence of an Ostium Secundum ASD and features of severe rheumatic mitral valve regurgitation. Child was initially placed on medications which included diuretics and an Angiotensin converting enzyme inhibitor ACEi, before she eventually had surgical closure of ASD and mitral valve replacement. The purpose of this case report is to highlight the symptomatology, diagnosis and treatment of this rare association, particularly in our environment.
										Abstract: Atrial septal defect (ASD) coexisting with mitral valve regurgitation has been described in literature with various aetiologies and pathophysiologic mechanisms. Mitral valve lesions coexisting with an ASD could either be congenital or acquired. The most prominent congenital mitral valve pathology is a cleft in the anterior leaflet of the mitral val...
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