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High-speed Video Microscopy Analysis for First-line Diagnosis of Primary Ciliary Dyskinesia
Published on: January 19, 2022
Cytomegalovirus pneumonia in an immunocompetent host with primary ciliary dyskinesia: A case report
Vasiliki Epameinondas Georgakopoulou1, Dimitrios Mermigkis2, Despoina Melemeni3
1Pulmonology Department, Laiko General Hospital, Athens. vaso_georgakopoulou@hotmail.com.
Abstract:
Primary ciliary dyskinesia (PCD) is an autosomal-recessive inherited disease caused by mutations in genes involved in ciliary structure and function leading to impaired mucociliary clearance and repeated or chronic, usually bacterial, infections of the upper and lower airways and decreased lung function and bronchiectasis. Cytomegalovirus (CMV) is a DNA virus that usually causes subclinical infection and in 10% of the patients causes a mononucleosis-like syndrome. CMV is a causative agent of serious illness in vulnerable immunocompromised groups such as transplant recipients, patients with immunodeficiency or malignancy and neonates. Life-threatening infection due to CMV, including CMV pneumonia, is not common in immunocompetent patients. In this report we describe a case of an otherwise immunocompetent woman, suffering from PCD, who developed severe CMV pneumonia.
Insights
Primary ciliary dyskinesia (PCD) patients can develop severe Cytomegalovirus (CMV) pneumonia, even if immunocompetent. This case highlights a rare but serious complication in individuals with impaired airway clearance.
Area of Science:
- Pulmonology
- Infectious Diseases
- Genetics
Background:
- Primary ciliary dyskinesia (PCD) is a genetic disorder impairing mucociliary clearance, leading to recurrent respiratory infections and bronchiectasis.
- Cytomegalovirus (CMV) typically causes mild or asymptomatic infections in immunocompetent individuals, but can cause severe illness in immunocompromised populations.
- Severe CMV pneumonia is uncommon in immunocompetent patients, making this case particularly noteworthy.
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