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BMJ Case Rep ; 13(9)2020 Sep 02.
Article in English | MEDLINE | ID: mdl-32878857

ABSTRACT

An 18-month-old boy presented with lytic lesion of skull and recurrent abscesses with Serratia marcescens The extensive work up revealed a gene mutation confirming the diagnosis of chronic granulomatous disease (CGD). This case scenario underscores the importance of exploring the possibility of immunodeficiency if there is a history of recurrent abscesses with atypical organism. The case also demonstrates that CGD can present as lytic lesion of skull.


Subject(s)
Abscess/immunology , Bone Diseases, Infectious/diagnosis , Granulomatous Disease, Chronic/diagnosis , Serratia Infections/immunology , Serratia marcescens/isolation & purification , Abscess/diagnosis , Abscess/microbiology , Abscess/therapy , Anti-Bacterial Agents/therapeutic use , Antibiotic Prophylaxis , Bone Diseases, Infectious/immunology , Bone Diseases, Infectious/microbiology , Bone Diseases, Infectious/therapy , Craniotomy , Diagnosis, Differential , Frontal Bone/diagnostic imaging , Frontal Bone/immunology , Frontal Bone/microbiology , Frontal Bone/surgery , Granulomatous Disease, Chronic/complications , Granulomatous Disease, Chronic/immunology , Histiocytosis, Langerhans-Cell/diagnosis , Humans , Infant , Magnetic Resonance Imaging , Male , Recurrence , Serratia Infections/diagnosis , Serratia Infections/microbiology , Serratia Infections/therapy , Serratia marcescens/immunology , Tomography, X-Ray Computed
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