CH 6 Pediatric Thorax Flashcards

1
Q

Neurogenic tumors

A

usually ganglioneuromas, arise posteriorly along sympathetic chain.

well-defined, hyperechoic, and have small granular calcifications. also associated with rib erosions.

neuroblastomas are the malignant form

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Neurenteric cysts

A

cysts of bowel that have failed to separate from the neural canal during development.

well-defined, thin-walled cysts in posterior chest. spinal anomaly seen higher than the lesion on x-ray. usually hypoechoic, may contain debris due to infection or hemorrhage.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Pulmonary sequestration (bronchopulmonary foregut malformation)

A

segment of lung which does not function due to an anomalous arterial blood supply with no communication with the tracheobronchial tree.

developmental abnormality where there is accessory tracheobronchial foregut bud.

lower lobe consolidation that never clears completely

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Intralobar pulmonary sequestration

A

ACQUIRED condition where abnormal lung is enclosed in the visceral pleura of the affected lobe.

presents: young adults following pneumonia, also associated with bronchial obstruction and compromised pulmonary artery supply.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Extralobar Pulmonary sequestration

A

CONGENITAL anomaly with pulmonary tissue with separate pleura and >60% have a diaphragmatic defect and CCAM of lungs.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Congenital pulmonary airway malformation (CPAM)
or
Congenital cystic adenomatoid malformation (CCAM)

A

mass of abnormal bronchial and lung tissue which develops within the fetal chest.

associated with polyhydramnios and hydrops in the fetus, due to tissue impinging on the esophagus and causing fluid backup.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Congenital pulmonary airway malformation (CPAM)
or
Congenital cystic adenomatoid malformation (CCAM)

3 types:

A

I: macrocystic- one or more large cysts measuring >2cm

II: mixed- multiple small cysts

III: microcysts- appears solid on u/s (no vascular supply) difference withpulmonary sequestration

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Pleural effusion

A

fluid in pleural cavity.

simple PE should appear anechoic and resolves with antibiotics

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

*Consolidation

A

lung appears hypoechoic.

Lung tissue solidifies due to fluid or exudate, as in pneumonia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Complicate Pleural effusion (PE)

A

usually due to bacterial infection and appear cloudy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Bacterial PE

A

have to be drained for resolution

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

*diaphragmatic hernia

A

defect in the diaphragm in which the abdominal contents herniate into the chest.
*more common on L due to liver acting as a plug.

may be congenital or acquired (trauma)

2 types: Bochdalek, morgagni

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Bochdalek hernia

A
  • approx 95% of congenital diaphragmatic hernias
    affects the back (posterior)

large, assoc. with pulmonary hypoplasia, prolapsed retroperitoneal fat, spleen and left kidney.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Morgagni hernia

A

affects the front (anterior)
small and rare
Occur later in life and bulge through sternocostal angles.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Diaphragmatic eventration

A

congenital anomaly, abnormal elevation of diaphragmatic dome.

diaphragm composed of fibrous tissue with little or no muscle fibers. region stretches on inspiration, does not contract normally.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

diaphragmatic paralysis

A

associated with damage to the phrenic nerve after thoracic surgery.
*Transducer placed intercostal rib space, vent should be disconnected for 5-10 seconds.

17
Q

malignant rhabdomyosacrcoma

A

rare tumor arising from the diaphragmatic muscle.

18
Q

Thymus

A

gland in superior mediastinum, anterior to ao arch.
*appearance of “sail”

special lymphnoid gland of the immune system. at puberty, thymus reaches height of its use, then declines as lympnoid tissue disappears and fat and fibrous tissue appears.

19
Q

Thymic cysts

A

usually unilocular and extremely uncommon.

may occur from the angle of the mandible to the thoracic inlet, more common on the left.

symptoms include; hoarseness, dysphagia, stridor and respiratory distress in newborns.

20
Q

superior herniation of the thymus

A

into the neck is rare. intermittent migration of the thymus out of the thorax into the suprasternal region occurs during valsalva.

21
Q

cervical ectopic thymus

A

very uncommon. Thymic tissue may be found along the thymopharyngeal duct or protrude into the chest wall due to a congenital sternal defect.

22
Q

Thymus may also be involved by the following

A

hemorrhage, hemangioma, leukemia, langerhans cell histiocytosis, lipoma, lymphatic formation, malignant infiltration of lymphoma or leukemia

23
Q

which gland has the appearance of a “sail”

A

Thymus gland

24
Q

which type of diaphragmatic hernia affects the front of the diaphragm?

A

morgagni

25
Q

Extralobar pulmonary sequestration

A

more common in males, 4x more common on the left, greater than 60% of children with this anomaly have a diaphragmatic defect.