Chronic granulomatous disease--a report in two Malay families.
- Author:
L Mohd NOH
1
;
R M NOAH
;
L L WU
;
B A NASURUDDIN
;
E JUNAIDAH
;
C P OOI
;
I ROSE
Author Information
1. Department of Paediatrics, Faculty of Medicine, Universiti Kebangsaan Malaysia, Kuala Lumpur.
- Publication Type:Case Reports
- MeSH:
Anti-Bacterial Agents;
therapeutic use;
Fatal Outcome;
Granulomatous Disease, Chronic;
diagnosis;
drug therapy;
immunology;
Humans;
Immunity, Cellular;
Infant;
Interferon-gamma;
therapeutic use;
Malaysia;
Male;
Phagocytosis
- From:Singapore medical journal
1994;35(5):505-508
- CountrySingapore
- Language:English
-
Abstract:
Chronic granulomatous disease (CGD) is a very rare disease whose defect lies in an abnormal intracellular killing resulting in recurrent abscesses, lymphadenitis and granuloma formation. We describe 2 Malay male infants with CGD whom we believe to be the first report of this disorder in Malays. Both children presented with recurrent abscesses, pneumoniae and hepatosplenomegaly; lymphadenopathy was also present in one of the patients. The organisms isolated were catalase positive bacteria. Both neutrophil chemiluminescence (against fungal and bacterial antigens, phorbol myristate acetate) and intracellular killing assays were severely depressed. Recognition of CGD is important as great strides have been made in the treatment of this disease which include gamma interferon therapy besides the conventional prophylactic antibacterial therapy.
