Rare Pulmonology News

Rare Pulmonology News Our mission is to inform the healthcare community about the diagnosis and management of rare diseases.

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🫁 Primary Ciliary Dyskinesia (PCD) is a rare genetic disorder affecting the tiny hair-like structures (cilia) in the res...
10/06/2025

🫁 Primary Ciliary Dyskinesia (PCD) is a rare genetic disorder affecting the tiny hair-like structures (cilia) in the respiratory tract, leading to chronic respiratory issues and recurrent infections. Early diagnosis and ongoing care are crucial for managing symptoms and improving quality of life. Learn more about PCD and its impact on health in this informative article.

Spotlight On Primary ciliary dyskinesia Primary ciliary dyskinesia (PCD) is an inherited disorder which affects the movement of tiny hair-like structures on body cells, known as cilia. Cilia are present on many types of cells, and particularly on those in the respiratory tract Stats & inheritance 5....

A fulminant lung disease with rapid onset respiratory failure and diffuse alveolar damage. Recognition and early interve...
09/19/2025

A fulminant lung disease with rapid onset respiratory failure and diffuse alveolar damage. Recognition and early intervention are crucial.

🩺 Study current pathology markers and management guidelines in this Rare View.

A rare and rapidly progressive form of idiopathic interstitial pneumonia, characterized by diffuse alveolar damage and acute respiratory failure. The prognosis is generally poor, with high mortality rates despite aggressive treatment.

A genetically inherited motile ciliopathy that impairs mucociliary clearance, leading to recurrent respiratory infection...
09/08/2025

A genetically inherited motile ciliopathy that impairs mucociliary clearance, leading to recurrent respiratory infections, laterality defects like situs inversus, and fertility challenges.

Enhance your clinical knowledge—understand PCD’s diagnostic complexity and current management strategies.

Explore the full Spotlight

Spotlight On Primary ciliary dyskinesia Primary ciliary dyskinesia (PCD) is an inherited disorder which affects the movement of tiny hair-like structures on body cells, known as cilia. Cilia are present on many types of cells, and particularly on those in the respiratory tract Stats & inheritance 5....

Which presentation is most commonly seen in patients with primary pulmonary lymphoma?Challenge your diagnostic skills wi...
08/21/2025

Which presentation is most commonly seen in patients with primary pulmonary lymphoma?

Challenge your diagnostic skills with this focused clinical question.

Our mission is to inform the healthcare community about the diagnosis and management of rare diseases. Help us by sharing this important information with your peers.

A hypersensitivity pneumonitis caused by repeated inhalation of moldy organic dust.Five concise facts to improve early r...
08/15/2025

A hypersensitivity pneumonitis caused by repeated inhalation of moldy organic dust.

Five concise facts to improve early recognition and intervention.

1 Farmer’s Lung Disease is a type of hypersensitivity pneumonitis, an allergic lung disease, triggered by repeated inhalation of moldy hay, straw, or other agricultural materials 2 It primarily affects individuals with prolonged exposure to moldy agricultural dust, such as farmers, causing an immu...

A rare, irreversible small airway disease often following severe lung injury or toxic exposure.Review the pathology, ris...
08/14/2025

A rare, irreversible small airway disease often following severe lung injury or toxic exposure.

Review the pathology, risk factors, and current management options.

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Spotlight On Bronchiolitis Obliterans Bronchiolitis Obliterans (BO), also known as Constrictive Bronchiolitis, is a rare, irreversible obstructive lung disease characterized by inflammation and fibrosis of the small airways, leading to airflow obstruction. Stats & inheritance 5 Facts Rare Views Inte...

Pulmonary amyloidosis is diagnosed primarily through tissue biopsy, often obtained via bronchoscopy or surgical lung bio...
05/14/2025

Pulmonary amyloidosis is diagnosed primarily through tissue biopsy, often obtained via bronchoscopy or surgical lung biopsy, which reveals amyloid deposits upon histological examination

1 Pulmonary amyloidosis is diagnosed primarily through tissue biopsy, often obtained via bronchoscopy or surgical lung biopsy, which reveals amyloid deposits upon histological examination 2 Imaging studies such as high-resolution computed tomography (HRCT) of the chest can show characteristic patter...

A rare, inherited immunodeficiency that affects certain white blood cells that leads to the formation of granulomas in m...
05/13/2025

A rare, inherited immunodeficiency that affects certain white blood cells that leads to the formation of granulomas in many organs

Spotlight On Chronic Granulomatous Disease (CGD) A rare, inherited immunodeficiency that affects certain white blood cells that leads to the formation of granulomas in many organs Stats & inheritance 5 Facts Rare Views Interest Signs & symptoms Current treatments Clinical trials Treatments in resear...

Allergic Bronchopulmonary Aspergillosis (ABPA) is a hypersensitivity reaction to the fungus Aspergillus fumigatus coloni...
04/02/2024

Allergic Bronchopulmonary Aspergillosis (ABPA) is a hypersensitivity reaction to the fungus Aspergillus fumigatus colonizing the airways, primarily affecting individuals with asthma or cystic fibrosis.

1 Allergic Bronchopulmonary Aspergillosis (ABPA) is a hypersensitivity reaction to the fungus Aspergillus fumigatus colonizing the airways, primarily affecting individuals with asthma or cystic fibrosis 2 ABPA presents with symptoms such as wheezing, coughing, shortness of breath, and production of....

How much do you know about Niemann-Pick disease type B? Take a deep dive into our quizzes, expand your medical knowledge...
04/02/2024

How much do you know about Niemann-Pick disease type B? Take a deep dive into our quizzes, expand your medical knowledge, and test your expertise with us!

Our mission is to inform the healthcare community about the diagnosis and management of rare diseases. Help us by sharing this important information with your peers.

Activated PI3K Delta Syndrome (APDS) is a rare, genetic primary immunodeficiency.
04/02/2024

Activated PI3K Delta Syndrome (APDS) is a rare, genetic primary immunodeficiency.

Spotlight On Activated PI3K Delta Syndrome (APDS) Activated PI3K Delta Syndrome (APDS) is a rare, genetic primary immunodeficiency Stats & inheritance 5 Facts Rare Views Interest Signs & symptoms Current treatments Clinical trials Treatments in research Prevalence < 1 / 1,000,000 < 331 US Estimated....

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