Related Experiment Video
Updated: Aug 21, 2025

06:57
The WinCF Model - An Inexpensive and Tractable Microcosm of a Mucus Plugged Bronchiole to Study the Microbiology of Lung Infections
Published on: May 8, 2017
9.3K
Bronchial mucus plug mimicking fragmented Ascaris worm: An ambiguous case presentation
Vibha Mehta1, Poonam S Loomba1, Bibhabati Mishra1
1Department of Clinical Microbiology, Govind Ballabh Pant Institute of Postgraduate Medical Education and Research, New Delhi, India.
Journal of Family Medicine and Primary Care
|November 17, 2022
Summary
Parasitic lung diseases can mimic common respiratory issues like mucus plugs, posing diagnostic challenges. Accurate diagnosis requires careful evaluation of clinical, radiological, and pathological findings to avoid unnecessary invasive tests.
Area of Science:
- Pulmonology
- Infectious Diseases
- Parasitology
Background:
- Increasing global travel and immunosuppression contribute to a rise in reported parasitic lung and pleural diseases.
- Diagnosis of parasitic lung diseases can be challenging due to nonspecific clinical and radiological presentations.
Related Concept Videos
The Bronchial Tree
3.3K
The human bronchi and bronchial tree play a crucial role in the respiratory system, facilitating the exchange of oxygen and carbon dioxide. Let's delve into the intricate structure and functions of these respiratory components.
The trachea, commonly known as the windpipe, is a tube that connects the larynx (voice box) to the bronchi. At a point called the carina, it bifurcates into two primary bronchi. The right primary bronchus is wider, shorter, and more vertical than the left primary...
The trachea, commonly known as the windpipe, is a tube that connects the larynx (voice box) to the bronchi. At a point called the carina, it bifurcates into two primary bronchi. The right primary bronchus is wider, shorter, and more vertical than the left primary...
3.3K
Cystic Fibrosis: Pathogenesis
329
Cystic fibrosis (CF), an autosomal recessive disorder, significantly affects the function of exocrine glands. This genetically inherited disease is characterized by the production of thick and sticky mucus, which can severely affect various organs and systems in the body.
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation,...
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation,...
329

