Background: Acute respiratory infections are a frequent reason for consultations in internal medicine. Unpredictable in their evolution, these infections can require hospitalization, and can constitute a medical emerg...
IgG4 disease is an immune-mediated disorder characterized by fibroinflammatory masses that can infiltrate multiple organ systems. Renal involvement is considered one of the key features of this disease. Report 02 case...
Inflammatory myofibroblastic tumor has been referred to by many different names in the past, such as plasma cell granuloma, inflammatory pseudotumor, fibrous histiocytoma, fibroxanthoma, xanthogranuloma. It was first ...
Introduction: Pheochromocytoma is a rare cause of secondary arterial hypertension whose clinical presentation can be multifaceted. In particular, it may be revealed or complicated by cardiovascular manifestations inde...
Myxomas are primary cardiac tumors of the most common pathology, with 75% of myxomas originating in the left atrium either at the mitral annulus or the fossa ovalis border of the interatrial septum;the remaining 20% c...
Introduction: The objective of this study was to evaluate the clinical characteristics of patients with coexistence of diabetes and liver disease in the internal medicine department of Donka University Hospital. Diabe...
Objectives: The objectives of this study were to determine the frequency of arterial hypertension and to describe its characteristics in diabetic patients followed in Guinea. Methods: This was a cross-sectional, descr...
Introduction: The objective of this study was to contribute to a better understanding of high blood pressure (HBP) and other cardiovascular risk factors associated with the internal medicine department of Donka Univer...
Bartonella species are bacterial pathogens responsible for Cat Scratch Disease (CSD) with various clinical manifestations, ranging from self-limiting febrile illnesses to severe systemic infections. Diagnosis is often...
Background: DiGeorge syndrome (also known as velo-cardio-facial syndrome) is a rare multisystem genetic disorder occurring in approximately 1 in 4000 to 1 in 6000 live births [1]. Although advances in genetic screenin...