1. Chest (Congenital) Flashcards

1
Q

Bronchial Atresia - Anatomy

A

Most commonly apical-posterior segment of left upper lobe.

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2
Q

Bronchial Atresia - imaging (2)

A

Blind ending bronchus, filled with mucus (finger in glove).
Distal lung hyperflated (from collateral drift and air trapping).

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3
Q

AVM - Cause (3)

A

Can occur sporadically.
HHT or Osler Weber Rendu

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4
Q

AVM - anatomy

A

more common in lower lobes (more vascularity)

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5
Q

AVM - clinical

A

Can be source of right to left shunt (source of stroke/brain abscess)

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6
Q

AVM - Rx

A

Treat once afferent vessel is 3mm

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7
Q

Persistent left SVC - anatomy (4)

A

Usually only significant if a line is inserted, line sits left paramedian.
Usually drains into coronary sinus.
5% drain into left atrium, causing mild right to left shunt (CT shows pacemaker or line going into right heart from left.

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8
Q

Persistent left SVC - Trivia

A

Commonest congenital venous abnormality of the chest.

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9
Q

Swyer-James - anatomy (3)

A

Classic unilateral left lung.
Occurs after viral lung infection in childhood, causing post infective obliterative bronchiolitis.
Size of affected lobe is smaller (not hyperexpanded).

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10
Q

Poland - anatomy (2)

A

Unilateral absence of pectoral muscle.
Associated with small arms/hands.

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11
Q

Poland - imaging

A

CXR shows hyperlucent chest on affected side.

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12
Q

Sequestration - types (2)

A

Intralobar (no pleural cover) and Extralobar (has pleural cover).
Cannot tell difference radiographically.

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13
Q

Intralobar sequestration (5)

A

More common (75%),
Presents in adolescents with recurrent infections.
Most commonly left lower lobe posterior segment (2/3), rarely affects upper lobes.
Rarely associated with other developmental abnormalities.
Pulmonary venous drainage

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14
Q

Extralobar sequestration (4)

A

Less common (25%),
Presents in infancy with respiratory compromise (mainly due to associated abnormalities)
Rarely infected as it has own pleural covering.
Systemic venous drainage.

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15
Q

Extralobar sequestration - associations (5)

A

CCAM (Congenital cystic adenomatoid malformation),
Congenital diaphragmatic hernia,
Vertebral anomalies,
Congenital heart disease,
Pulmonary hypoplasia

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16
Q

CCAM - anatomy (3)

A

Malformation of adenomatoid which replaces normal lung.
Usually only affects one lobe.
Communicate with airway, therefore filling with air.

17
Q

CCAM - types (3)

A

Type 1 = cystic
Type 3 = solid,
Type 2 = intermediate

18
Q

CCAM - Rx (2)

A

90% decrease in size by third trimester.
Rx is surgical removal, due to risk of malignant transformation (retropulmonary blastoma, rhabdomyosarcoma)

19
Q

Systemic artery feeding a CCAM?

A

Not a CCAM, it’s a sequestration.