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238
M. Riccabona
Table 12.1 (continued)
Lung sliding Sliding of lung
surface, best documented by video clip
Pleural line White line,
underneath chest wall, visceral + parietal pleura. DDx: peripheral dystelectasis (use HR Tdx)
Normal ventilation
Thick line, irregular; possibly + effusion (thin line = normal)
Quad sign Fluid surrounded
Ring-down artefact
Seashore sign Lung sliding,
Shred sign Deeper incomplete
Sinusoid sign On M-mode: lung
Tissue sign “Hepatisation” =
by four borders (pleural line, rib shadow, lung)
Condensed or grouped B-lines If very dense = “lung rockets”
documented by M-mode
set of lines due to irregular borders
moves in a sinusoid pattern with breathing
liver-like US appearance of non-ventilated lung parenchyma
Seen in effusions similarities with “bat sign”
1–3 normal >3 = pathology
Normal ventilation
Soft tissue “mass”, atelectasis, subpleural consolidation, etc.
M-mode pattern of e.g. effusion with unimpaired respiratory motion
For example, in pneumonia, total atelectasis, tumour, etc.
12 Ultrasound oftheChest
Table 12.1 (continued)
White lung So many B-lines
that cannot be differentiated and entire lung is echogenic
Adapted from “Bildgebung des Thorax bei Neugeborenen und Kleinkindern” (Riccabona M, Beer M, Mentzel HJ. eds): Chapter 4, Sonograe des Früh- und Neugeborenen-, bzw. Säuglingsthorax, Tab. 1. Springer 2019, p.35; Some US images courtesy of B.Coley, Cincinnati, Ohio, USA
Severe hypoination/no aeration: (I/A)RDS, if only basal “wet lung”, “white lung” during ECMO, etc.
239
12.2.6 Mediastinum
12.2.6.1 Anterior Mediastinum/Thymus
Mainly Thymus (Fig.12.3):
• Physiologically large in neonates, then eventually regresses.
• Shape and size variable.
• Echogenicity: hypoechoic, mixed, with some septa (“dot-dash pattern”).
• Behaviour of soft tissue: not compressing or displacing other structures, particu-
larly vessels.
• Size of thymus difcult to assess, reliable age-related normal values not available.
• CDS: some internal vascularity.
Value of US:
• Differentiate from other mediastinal or chest masses (unclear opacication on
chest lm).
• Demonstrate normal echogenicity and behaviour in relation to surrounding
structures of a large thymus.
• Additionally: ideal acoustic window to deeper structures (vessels, middle and
posterior mediastinum, hilar area and oesophagus, etc.).
Note Large thymus at unusual age may point at diffuse inltration or thymus
hyperplasia; inltration and tumours will cause increased stiffness and thus subse­quent impression or displacement of surrounding structures or crossing vessels.
12.2.6.2 Middle Mediastinum
Contains—among others—large vessels, trachea, potential nodes may be visualised by US (Fig.12.4):
• Particularly feasible in neonates and infants.
• Large space-occupying lesions, tumours or lymph node enlargement visible.
• Anatomy of large vessels addressed with echocardiography.
240
Fig. 12.3 Thymus: (a) Anterior mediastinum, axial section, linear transducer: Large neonatal thymus, serving as window to deeper structures such as the great vessels. Note non-ossied ster­num with central ossication centre. (b) Sagittal section, anterior and middle mediastinum, linear transducer in trapezoid format, paramedian view: Large neonatal thymus. Note anechoic non­ossied parts of ribs and large, uncompressed vessels; behind one can see a feeding tube in the oesophagus. (c) Left anterior mediastinum, axial section, sector transducer: Enlarged thymus with inhomogeneous echogenicity in nodular-patchy fashion in a child with Hodgkin lymphoma. (d) Right anterior mediastinum, axial section, linear transducer in trapezoid format: US in mediastini­tis, abscess-like pseudotumourous inammatory lesions with nodular appearance in the mediastinum
M. Riccabona
Fig. 12.4 Middle mediastinum: vessels and lymph nodes. Parasternal (jugular) sagittal view, sector transducer: thoracic aortic arch, supra-aortic vessels, two enlarged mediastinal lymph nodes (dotted circular lines)
12 Ultrasound oftheChest
241
12.2.6.3 Posterior Mediastinum
Difcult to visualise by US.
Usually anterior access supplemented by posterior paravertebral access.
Used for assessing tumours, particularly neuroblastoma.
12.2.7 (Colour) Doppler Sonography
Except for assessment of vessels, CDS not very useful in normal situation.
Indications for chest CDS mostly for DDx in pathology, mostly of the lung: e.g. abscess or necrosis, tumour vascularisation, vascular or other malformations, suspected particularly peripheral pulmonary artery embolism (PAE, resemble tri­angular subpleural pneumonic areas without depictable vascularisation), etc.
12.2.8 Contrast Enhanced US (ce-US)
CEUS and ce-US can be used in the paediatric chest, though presently (still?) off­label—sometimes helpful, also depending on quality of equipment and if relevant ndings with therapeutic consequence can already be seen without US con­trast agents.
Indications for iv.-CEUS are assessment of necrotic areas in pneumonia, whereas the intracavitary application of the US contrast agent (ce-US) via drain may help in assessing empyema or connections between uid-lled compartments (see Fig.12.10d, e).
12.3 Pathology ofChest Wall
12.3.1 Aplasia: Variations ofRibs
Quite common, cartilaginous part nicely assessed by US, wide range of rib anomalies:
• 3DUS reconstructions improve understanding and visualisation (see respective
chapter).
• Plain lm: US complements plain lm.
12.3.2 Congenital Malformations
Vascular malformations (lymphangioma, haemangioma), other soft tissue masses— see below:
• Reect typical US appearance elsewhere (see respective chapters).
242
M. Riccabona
12.3.3 Traumatic Changes
Fractures of ribs and sternum: see chapter on musculoskeletal US.
• Particularly in cartilaginous parts and sternum
– US may be superior to plain lm, where these structures are difcult to assess
if not signicantly displaced.
Note Follow entire structure in axial and longitudinal sections to detect any surface
interruption/irregularity.
Often some reactive focal subperiosteal haematoma:
• Without history, differentiation from osteomyelitis difcult.
• Particularly if bilateral, multiple, of different age—NAI should be considered.
Additional Findings
• Complicated haemorrhagic pleural effusion, atelectasis.
• Haematoma: seen in all chest wall spaces, usually no indication for imaging—
only in unclear cases, complicated course, suspicion of infection (DDx: seroma,
myositis ossicans, etc.).
12.3.4 Chest Wall Tumours
12.3.4.1 Lymphangioma (Venolymphatic Vascular Malformation)
US Finding
Multicystic space-occupying lesions with echogenic septae.
• Spontaneous haemorrhages with uid–uid levels often present.
• CDS: potentially some vessels within septae.
12.3.4.2 Lipoma
US Finding
Usually slightly inhomogeneous, echogenic mass, sharp margins (Fig.12.5).
12.3.4.3 Fibroma/Neurofibroma
US Finding
Usually sharp margin, hyperechoic or inhomogeneous.
a
12 Ultrasound oftheChest
243
b
cd
Fig. 12.5 Chest wall US: (a) Chest wall lipoma: well-dened subcutaneous mass (+ +), fat-like intermediate density echoes. (b) Below lipoma mass, structures of chest wall can be appreciated: muscle and ossied ribs (shadowing). (c, d) Thoracic inlet syndrome: compression (arrow) of the subclavian vein (c), with secondary subclavian and axillary vein thrombosis (i.e. mass in vessel, no ow on CDS) (d)
Fig. 12.6 Chest wall tumour—Askin tumour/Ewing sarcoma. Extended eld of view US demonstrates large chest wall tumour with calcied part (dorsal shadow) arising from partially destructed rib
12.3.4.4 Other Tumours
Rare; e.g. rhabdomyosarcoma or Ewing sarcoma (Fig.12.6):
• Sometimes difcult to differentiate from myositis ossicans, particularly
Askin tumour.
US Finding
No specic sonographic features.
12.3.5 Breast
Breast US In childhood of limited importance (see also chapter small part US).
244
M. Riccabona
Neonates Transient physiologic swelling, cystic duct ectasia and cysts seen.
• Secondary infection with abscess formation and haematoma may occur
(Fig.12.7b).
(Pre-)puberty cysts, tubular duct ectasia, broadenoma, inammatory formations
(Fig.12.7c):
• Overall appearance varies with age and maturation (Fig.12.7a, d).
• Most pathological entities do not differ from typical US appearance in adults.
Additional application of breast US in childhood: Assessment of sexual matura­tion, documenting presence and size of breast tissue.
• In girls with suspected hormonal or genetic pathology
• In boys with gynaecomastia
– In some centres proof of signicant breast tissue necessary for treatment
decision.
Note Breast carcinoma extremely rare in childhood.
CDS Can be helpful for assessment of supercial tumours or vascular malforma-
tions and other pathology described in respective chapters.
a
c
Fig. 12.7 Breast US in childhood: (a) Normal breast tissue. (b) Neonatal breast abscess—huge collection with membrane-like border and adjacent soft tissue reaction (hyperechoic, swelling) after neonatal mastitis; note plenty of US gel to facilitate transducer coupling to tissue without interposing air. (c) Impressive cystiform duct ectasia in a breast feed infant. (d) Asymmetric promi­nent breast tissue at onset of pubarche in 11-year-old girl
d
b
12 Ultrasound oftheChest
245
12.3.6 Miscellaneous Other Applications
Other potential applications in “lumps and bumps” of chest wall addressed in chap­ter on musculoskeletal and small part US.
Additionally vascular queries may arise—e.g. thoracic inlet/outlet syndrome (Fig.12.5c, d).
12.3.7 Role ofUS andAdditional Imaging
US Supplementary tool in clinically equivocal situation, follow-up.
Additional Investigations
• Suspicion of tumour—depending on oncology protocols—plain lm, CT/MRI.
• Assessment of osseous structures: plain lm, rarely CT.
• Mammography: very rarely indicated, and only in/after puberty.
12.4 Pathology ofPleural Space
12.4.1 Pneumothorax
Detection by US is possible and benecial for patients in the emergency department (ER) and on ventilation support (NICU, ICU, etc.).
US Findings
• To-and-fro motion during respiration in real-time US with B-mode (visceral
pleura or parietal pleura) “gliding” or “sliding” sign and M-mode “seashore”
sign (see also Table12.1).
• Additional ndings: lung point, absence of B-lines and absence of lung pulse.
• Pneumothorax directly beneath the US transducer: no sliding sign in B-mode
and “stratosphere” sign on M-mode (see Fig.12.21e and Table12.1).
False-positive ndings from hyperextended hyperinated lung (COPD,
Note
severe asthma, air trapping, aspiration with focal emphysema/hyperination, etc.).
12.4.2 Pleural Effusion
Denition
Some uid in between two pleural sheets of varying aetiology:
• Cardiac, inammation, trauma, tumour, etc.
• Most common pleural change, most common indication for chest US.
246
M. Riccabona
US Findings
Simple pleural effusion: Unechoic uid without septae (Fig.12.8).
Complicated effusion: Fluid contains oating echoes, septae, complex nature
(Fig.12.9):
– Depends on haemorrhage, chronicity and recurrence, empyema, etc. – Denite diagnosis of underlying entity not achievable by US.
Note Quantication of pleural effusion limited. If US used for follow-up (to deter-
mine increase or decrease of amount of uid)—use standardised views and positioning:
• Possibly in sitting or upright position.
• US aspect changes signicantly with posture—with redistribution of uid,
depending on position.
12.4.2.1 Empyema
Denition and US Findings
Complex effusion with multiple septae which may contain vessels (Fig.12.9b):
• Some space-occupying component.
• May compress adjacent lung—often associated with or even caused by pneumo-
nia, atelectasis and abscess.
(a)CDS Peripheral and septal hyperaemia.
ce-US Via a pleural drain US contrast agent can be instilled to observe connections
between the various compartments, e.g. for monitoring during brinolytic therapy; non-communicating compartments may need a separate drain.
Fig. 12.8 Simple pleural effusion: (a) Axial view: Small amount of simple pleural effusion (+ +) in pleuritis: the little amount of effusion better visualised on US than on plain lm. Note pleural thickening. (b) Sagittal dorsal view in upright sitting child for standardised assessment: simple pleural effusion—height (+….+) can be measured. (c) Axial view through liver, transducer tilted cranially: bilateral simple pleural effusions in a neonate—US cannot differentiate kind and entity (e.g. chylothorax)
12 Ultrasound oftheChest
Fig. 12.9 Complicated pleural effusion and empyema: (a) Axial intercostals view with sector transducer: complex uid with oating echoes in complicated pleural effusion, lung compressed and not aerated; US does not allow for differentiation of entity (e.g. haemorrhage versus inamma­tion). (b) Axial section: Complicated effusion with cystic areas in pleural empyema; NOTE: Atelectasis of adjacent pneumonic lung
247
DDx Any other complex uid, most important entities:
• Subphrenic/subpulmonic abscess, lung abscess (may exist concurrently).
• Complex pericardial effusion.
• Haemorrhagic bronchogenic cyst.
• Complex echinococcal/hydatid cyst.
• Thoracic lymphangioma.
• Ventral meningocele (usually clear uid, posterior mediastinum).
• Duplication cyst.
• Cystic extasia of the lymphatic duct (Fig.12.10d, e).
12.4.3 Other Pleural Pathology
Thickening of pleura: after surgery/inammation.
Space-occupying lesions/tumours of pleura: extremely rare in children.
• Few entities reported: – Pleural mesothelioma, pleural carcinosis, inltration by metastases. – Penetration from pulmonary as well as abdominal tumours (Fig.12.10). – No specic US ndings.
12.4.3.1 Role ofImaging
Role/Value of US
• More sensitive than plain lm or even CT for detection of minimal pleural effu-
sions—gold standard for diagnosis and follow-up.
• Ideal complementary imaging tool for assessing equivocal opacities on plain lm.