منابع مشابه
A chronic granulomatous disease of childhood.
A 5-year-old g rl presented w th a five-month h story of low grade fever and arthralg a w th decreased energy level. Exam nat on revealed arthr t s affect ng both ankles and knees as well as hepatosplenomegaly. Funduscop c exam nat on showed poster or granulomatous uve t s (F gure 1). Synov al b opsy revealed synov al prol ferat on w th non-necrot z ng granulomas (F gure 2). A Chronic Granuloma...
متن کاملMonocyte function in patients with chronic granulomatous disease of childhood.
Adults with chronic granulomatous disease of childhood (CGD) have been described who remain relatively free of infection despite markedly abnormal neutrophil function. Monocyte function in four adults with this mild or atypical CGD syndrome was examined and compared to that of normal controls and to that of two patients with the more severe or classic CGD syndrome. Monocytes from patients with ...
متن کاملChronic Granulomatous Disease, Case Report and Review of Literature
Chronic granulomatous disease (CGD) is a rare inherited disorder characterized by inability of phagocytes to generate oxygen radicals needed for intracellular killing of phagocytic microorganisms. We report a 2.5-year-old Iranian female with multiple liver abscesses. She was admitted in surgical ward because of abdominal pain and fever for one month duration that had no response to conventio...
متن کاملChronic bullous disease of childhood and a paecilomyces lung infection in chronic granulomatous disease.
A 12 year old boy suffering from p67-phox deficient chronic granulomatous disease presented with a bullous skin disease and a lung infection with paecilomyces species. The histopathology of a bullous lesion showed subepidermal blister formation and microabcesses containing eosinophils in the dermal papillae. By direct immunofluorescence, linear staining of IgA at the dermal-epidermal junction w...
متن کاملChronic Granulomatous Disease
Background: Chronic granulomatous disease (CGD) is an uncommon primary immunodeficiency that can be inherited in an X-linked (XL) or an autosomal recessive (AR) manner. We reviewed our large, single-center US experience with CGD. Methods: We reviewed 27 patients at Ann & Robert H. Lurie Children's Hospital of Chicago from March 1985 to November 2013. Fisher exact test was used to compare differ...
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ژورنال
عنوان ژورنال: American Journal of Roentgenology
سال: 1968
ISSN: 0361-803X,1546-3141
DOI: 10.2214/ajr.103.1.133