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Published on: October 21, 2014
[Clinical features and early diagnostic clues of chronic granulomatous disease]
1Department No.2 of Respiratory Medicine, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing 100045, China.
Insights
Early diagnosis of chronic granulomatous disease (CGD) in children is crucial. Key clinical clues like large BCG scars and recurrent infections can significantly shorten diagnosis time and reduce healthcare costs.
Area of Science:
- Pediatrics
- Immunology
- Infectious Diseases
Background:
- Chronic granulomatous disease (CGD) is a primary immunodeficiency characterized by impaired phagocyte function.
- Delayed diagnosis of CGD leads to increased morbidity and mortality due to recurrent, severe infections.
- Identifying early clinical indicators is essential for timely diagnosis and management of CGD.
Purpose of the Study:
- To identify and evaluate early clinical clues for the diagnosis of chronic granulomatous disease (CGD) in children.
- To assess the impact of utilizing these early diagnostic clues on the time to diagnosis and healthcare utilization.
Main Methods:
- Retrospective analysis of clinical features of 139 children diagnosed with CGD between January 2007 and October 2020.
- Evaluation of clinical manifestations, age of onset, reasons for hospitalization, and diagnostic delays.
- Comparison of diagnostic time, length of stay, and hospital charges between patients diagnosed before and after 2015, following the identification of early diagnostic clues.
Main Results:
- CGD onset was typically early (74.1% before 1 year), with a median diagnostic delay of 1 year.
- Pulmonary infections were the most common presentation (97.1%), often with misdiagnosis rates as high as 96.3%.
- Eight key early diagnostic clues were identified: large BCG scar, left axillary lymphadenopathy/calcification, skin/lymph node infections, skin scars, multiple lung nodules, perianal abscess, and pulmonary infections with Aspergillus or Burkholderia.
Conclusions:
- CGD often presents in young children with significant diagnostic delays, primarily due to recurrent pulmonary infections.
- The identified early clinical clues, including specific infection patterns and physical findings, can significantly aid in the early diagnosis of CGD.
- Implementing these early diagnostic clues led to shorter diagnosis times, reduced hospital stays, and lower charges in the post-2015 cohort.
Abstract:
Objective: To explore the early clinical clues for diagnosis of chronic granulomatous disease (CGD). Methods: One hundred and thirty-nine children with CGD seen in Beijing Children's Hospital from January 2007 to October 2020 were included in this study. The clinical features including age of onset, first presentations, reason for being hospitalized, etiology, imaging features, clues for early diagnosis of all patients were evaluated retrospectively. According to the time of diagnosis, the patients were divided into two groups, cases diagnosed before 2015 and after 2015 and 2015. The time of diagnosis, the length of stay and the hospital charges were compared between the two groups. T test and χ2 test were used for statistical analyses. Results: One hundred and nineteen of the cases were males and 20 were females. The age of onset was 4 months (8 d to 14 years), and 103 cases (74.1%) had onset before 1 year of age. The age at diagnosis was 1.8 years (21 d to 14.7 years), and the time of diagnosis delay was 1 year (7 d to 13.7 years). One hundred and thirty-five cases (97.1%) had pulmonary infection as the main reason for hospitalization, of whom 76 cases (56.3%) had positive pulmonary etiology. One hundred and thirty-six patients (97.8%) were referred cases, of whom 5 were suspected of CGD before referral, and the misdiagnosis rate was as high as 96.3% (131/136). Eight early clues for diagnosis were found, the frequency from high to low, large bacillus Callmette-Guer scar in 99 cases (70.5%), left axillary lymphadenopathy or calcification in 73 cases (52.5%), skin or other lymph node infections in 58 cases (41.7%), skin scars in 50 cases (36.0%), multiple lung nodules in 42 cases (30.2%), perianal abscess in 35 cases (25.2%), pulmonary Aspergillus infection in 26 cases (18.7%) and pulmonary Burkholderia infection in 15 cases (10.8%). A total of 120 cases of CGD were diagnosed by respiratory burst test during hospitalization, including 55 cases diagnosed before 2015 and 65 cases diagnosed after 2015. After using these 8 early diagnosis clues, the cases diagnosed after 2015 had shorter time of diagnosis and the length of stay and lower hospitalization charge than cases diagnosed before 2014, and the difference was statistically significant ((25±7) vs. (10±5) d, (29±7) vs. (18±6) d, (3.7×104±1.2×104) vs. (3.2×104±1.2×104) Yuan, t=13.763, 9.262, 2.381, all P<0.05). Conclusions: Patients with CGD are younger at onset and the diagnosis is delayed. Pulmonary infections are the most common. Large BCG scar, left axillary lymphadenopathy or calcification, skin or other lymph node infections, skin scars, multiple lung nodules, perianal abscesses, pulmonary Aspergillus infection and Burkholderia infection can help early diagnosis of CGD.
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