scholarly journals Biventricular infective endocarditis in an immunocompetent adult patient with a congenital ventricular septal defect: a case report

2018 ◽  
Vol 2 (1) ◽  
Author(s):  
Muhammad Azam Shah ◽  
Abdulaziz Ali Ahmed Alghamdi ◽  
Saif Hasan Alogabey ◽  
Mohammad Bara Qattea ◽  
Iftikhar Ahmed Bajwa
Keyword(s):  
Case Report ◽  
Infective Endocarditis ◽  
Ventricular Septal Defect ◽  
Adult Patient ◽  
Septal Defect ◽  
Immunocompetent Adult

scholarly journals Gemella hepatic abscesses: a case report and review of the literature

2018 ◽  
Vol 12 (02) ◽  
pp. 146-149
Author(s):  
Rita Wilson Dib ◽  
Mireille Matar ◽  
Rami Hallak ◽  
Anna Farra ◽  
Jacques Mokhbat
Keyword(s):  
Case Report ◽  
Infective Endocarditis ◽  
Adult Patient ◽  
Surgical Approach ◽  
Human Disease ◽  
Liver Trauma ◽  
Review Of The Literature ◽  
Immunocompetent Adult ◽  
Brain Abscesses ◽  
Blunt Liver Trauma

Gemella haemolysans is a rare cause of human disease, namely infective endocarditis and brain abscesses. We report herein a case of Gemella haemolysans liver abscess in an immunocompetent adult patient secondary to blunt liver trauma and successfully managed by medical-surgical approach.

A Case Report of Infective Endocarditis that Caused by Gemella Haemolysans in a Patient with Ventricular Septal Defect

2000 ◽  
Vol 30 (12) ◽  
pp. 1574 ◽  
Author(s):  
Yoon Cheol Kim ◽  
Min Su Lee ◽  
Bo Young Kim ◽  
Jung Woo Lee ◽  
Dae Seung Lim ◽  
...  
Keyword(s):  
Case Report ◽  
Infective Endocarditis ◽  
Ventricular Septal Defect ◽  
Septal Defect

Management of Platelets in a Persian Girl with the Tetralogy_Pantalogy of Fallot (Tof_Pof): A Case Report Study

2020 ◽  
Author(s):  
Bahram Alamdary Badlou
Keyword(s):  
Case Report ◽  
Ventricular Septal Defect ◽  
Atrial Septal Defect ◽  
Sleep Disorders ◽  
Social Life ◽  
Rare Case ◽  
Septal Defect ◽  
Old Persian ◽  
Underlying Mechanisms ◽  
The Relationship

We report a rare case of unrepaired Tetralogy_Pantalogy of Fallot (TOF_POF) in a 20 years old Persian girl Mrs Zeynab S., who presented with cyanotic finger tops appearance, ongoing chronic thrombolytic destruction processes, and remarkable thrombocytopenia [1,2], heart ventricular septal defect (VSD), and might atrial septal defect (ASD), anxiety, sleep disorders, nightmares, and limited social life. Additionally, the relationship between underlying mechanisms, possible treatments of the thrombocytopenia, erythrocytosis, and unrepaired cardiovascular leakages remains unknown.

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