We describe the spectrum of radiologic appearances of hepatic abscesses in patients with chronic granulomatous disease (CGD), a hereditary immunodeficiency presenting in childhood that occurs at a rate of 1 in 200,000-250,000 live births and predisposes patients to infection with catalase-positive organisms. CONCLUSION: Hepatic abscesses in patients with CGD show an atypical radiologic appearance compared with sporadic hepatic abscesses, and they are characterized by homogeneous enhancement and multiseptal enhancement. In the appropriate clinical setting, the appearance of an enhancing mass should suggest the possibility of a CGD-related hepatic absces
Liver abscesses in chronic granulomatous disease (CGD) are typically difficult to treat and often re...
AbstractA 73-year-old patient with necrotizing granulomatous inflammation of the liver is presented....
Chronic granulomatous disease (CGD) is a rare inherited immunodeficiency disorder, characterized by ...
We describe the spectrum of radiologic appearances of hepatic abscesses in patients with chro...
Chronic granulomatous disease (CGD) is a rare congenital disorder characterized by repeated b...
The contribution of computed tomography (CT), ultrasound (US), and nuclear medicine studies in the e...
Chronic granulomatous disease (CGD) is a rare primary immunodeficiency disease, affecting phagocytic...
Abstract Background Chronic granulomatous disease (CGD), a rare inherited disorder, is characterized...
Chronic granulomatous disease (CGD) is a rare inherited disorder characterized by inability of phago...
The purpose of this pictorial essay is to present and summarize findings of various images of chroni...
Chronic granulomatous disease (CGD) is a primary immune deficiency causing predisposition to infecti...
Bacterial hepatic abscess usually is acute and progressive, often resulting in sepsis, impairment of...
AbstractPyogenic liver abscess (PLA) in children may be difficult to diagnose correctly, particularl...
Chronic granulomatous disease (CGD) is a rare inherited disorder caused by defective nicotinamide ad...
Diffuse liver disease, including all causes of chronic liver disease, affects tens of millions of pe...
Liver abscesses in chronic granulomatous disease (CGD) are typically difficult to treat and often re...
AbstractA 73-year-old patient with necrotizing granulomatous inflammation of the liver is presented....
Chronic granulomatous disease (CGD) is a rare inherited immunodeficiency disorder, characterized by ...
We describe the spectrum of radiologic appearances of hepatic abscesses in patients with chro...
Chronic granulomatous disease (CGD) is a rare congenital disorder characterized by repeated b...
The contribution of computed tomography (CT), ultrasound (US), and nuclear medicine studies in the e...
Chronic granulomatous disease (CGD) is a rare primary immunodeficiency disease, affecting phagocytic...
Abstract Background Chronic granulomatous disease (CGD), a rare inherited disorder, is characterized...
Chronic granulomatous disease (CGD) is a rare inherited disorder characterized by inability of phago...
The purpose of this pictorial essay is to present and summarize findings of various images of chroni...
Chronic granulomatous disease (CGD) is a primary immune deficiency causing predisposition to infecti...
Bacterial hepatic abscess usually is acute and progressive, often resulting in sepsis, impairment of...
AbstractPyogenic liver abscess (PLA) in children may be difficult to diagnose correctly, particularl...
Chronic granulomatous disease (CGD) is a rare inherited disorder caused by defective nicotinamide ad...
Diffuse liver disease, including all causes of chronic liver disease, affects tens of millions of pe...
Liver abscesses in chronic granulomatous disease (CGD) are typically difficult to treat and often re...
AbstractA 73-year-old patient with necrotizing granulomatous inflammation of the liver is presented....
Chronic granulomatous disease (CGD) is a rare inherited immunodeficiency disorder, characterized by ...