Mucoid impaction, also referred to as mucus plugging, mucous plugging, bronchial mucocele or bronchocele formation, refers to airway filling by mucoid secretions and can be obstructive or non-obstructive. It is a common pathological finding in chest imaging.
Mucoid impaction may result from either obstructive or non-obstructive causes, although the latter does eventually obstruct the bronchi as well:
Non-obstructive causes are infectious or inflammatory in nature:
- cystic fibrosis: due to impaired ciliary movement and thick secretions
- asthma: due to increased mucus production
- allergic bronchopulmonary aspergillosis (ABPA)
- other acquired conditions
Mucoid impaction may appear as a branching tubular opacity that is distinct from the normal vascular shadows.This classic feature is the finger-in-glove sign, and is also seen on CT. It can sometimes prove difficult to diagnose on plain radiography.
The appearance on CT can be variable, depending on where the mucous plugging occurs (i.e. central or peripheral airways).
Mucous plugs appear as fluid density material often located dependently within the bronchus, sometimes with internal gas.
The classic feature seen when plugged mucus extends along large branching airways is the finger-in-glove sign.
Several key additional features can also occur:
- distal lung collapse: from collateral air drift; this has not yet developed in infants and young children, which is why the distal lung is rather hyperlucent in this population (e.g. congenital bronchial atresia, foreign body aspiration)
- distal airway dilatation
- double artery sign 9
Treatment and prognosis
Prolonged mucous plugging can lead to bronchial dilatation and bronchiectasis.
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