1.An intracardiac mass was incidentally detected during echocardiography in a patientundergoing preoperative assessment. Chest X-ray was non specific, showing an enlarged heart.Which one of the following statements regarding primary benign cardiac tumours is false?
A. Cardiac fibromas are homogenously low on T2W MRI.
B. Cardiac lipomas are high on T1W MRI.
C. Cardiac rhabdomyomas are associated with tuberous sclerosis.
D. Cardiac fibroelastomas usually arise from the pericardium.
E. Cardiac myxomas show heterogeneous signal on MRI.
1.D. Cardiac fibroelastomas usually arise from the pericardium.
Most lipomas appear to be subepicardial, expanding into the pericardial space. They typically have high signal on T1-weighted images and low signal on fat-suppressed images.
Fibroelastomas occur on cardiac valves, making them the most common neoplasm of the valves.They are hypointense mobile masses situated away from the free edge of the valves.
Fibroma is a neoplasm primarily of infants and children. Fibromas are homogeneouslyhypointense on T2-weighted images and show variable enhancement.
Rhabdomyomas are the most common benign cardiac tumour of childhood associated withtuberous sclerosis. They originate within the myocardium, typically in the ventricles, may be multiple, and are high on T2-weighted images.
The majority of myxomas manifest in adulthood between the fourth and seventh decades.
A minority will constitute part of an autosomal dominant syndrome known as Carney complex, characterised by myxomas, hyperpigmented skin lesions and extracardiac tumours such as pituitary adenomas, breast fibroadenomas and melanotic schwannomas. The classic triad of symptoms attributed to myxomas include cardiac obstructive symptoms related to obstruction to blood flow, embolic events and constitutional symptoms such as fever, malaise and weight loss. At MR imaging, the vast majority of myxomas demonstrate heterogeneous signal intensity.
The main differential diagnoses for myxoma include atrial thrombus or papillary fibroelastoma. Myxomas are more likely to arise anteriorly from the interatrial septum, whereas thrombus is more likely located posteriorly in the left atrium. In addition, myxomas enhance with gadolinium contrast material, whereas thrombi, in most cases, do not.
@# 2.A 40-year-old man undergoes a CT scan of the abdomen for recurrent abdominal pain.
The precontrast scan showed bilateral renal calculi. A post-contrast scan showed severalpancreatic lesions, measuring between 1 and 2 cm. What is the likely unifying diagnosis?
A. MEN I
B. MEN IIA
C. Insulinoma
D. Glucagonoma
E. NF1
2.A. MEN 1
Multiple endocrine neoplasia Type 1 is also known as Wermer syndrome. Inheritance isautosomal dominant with high penetrance. The male to-female ratio is 1:1. Organ involvement includes parathyroid hyperplasia (97%), pancreatic islet cell tumour (30% 80%), anterior pituitary gland tumour (15%—50%) and adrenocortical hyperplasia (33%-40%).
3.A 45-year old woman presents with a rapidly enlarging mildly painful breast mass over
a period of few months. An urgent ultrasound is performed. The ultrasound shows that themass measures 7 cm, filling up almost the entire breast with fluid-filled clefts in thetumour. What is the diagnosis?
A. Inflammatory carcinoma
B. Cystosarcoma phylloides
C. Complex breast cyst
D. Invasive lobular carcinoma
E. Breast lymphoma
Phylloides tumour (PT) is a rare breast fibroepithelial neoplasm.
It is now generally accepted that PTs can be classified as benign, borderline or malignant.
Mammography and ultrasound are notorious for their inability to distinguish the benign or malignant histologic nature of PTs.
On US, they can be indistinguishable from fibroadenoma. They appear as an inhomogeneous, solid-appearing mass. A solid mass containing single or multiple, round or cleft-like cystic spaces and demonstrating posterior acoustic enhancement strongly suggests a diagnosis of PTs.Solid components of the tumour show vascularity on Doppler.
On MRI, well-defined margins with a round or lobulated shape and a septate inner structure have been described as characteristic morphologic signs. They are usually low on T1-weighted images and vary from low to very high signal on T2-weighted images. Some have described a silt-like pattern on MRIs of benign PTs; these appear as hyperintense slit-like fluid-filled spaces on T2-weighted images, with a low signal after enhancement. Solid areas of the tumour show enhancement with contrast.
4.Osteoid osteomas:
A. Are aggressive bone lesions with malignant potential
B. Are referred to as osteoblastomas when larger than 3 cm
C. Are typically cortical rather than subcortical based lesions
D. Typically require surgical curettage and resection
E. Are more common in women
Osteoid osteomas are benign and aggressive bone tumours that are more common in men and usually present clinically in patients less than 30 years of age.
They are most commonly based within the cortex, although they can also occur in any other area of the bone.
When larger than 2 cm, they are regarded as osteoblastomas.
Radiofrequency ablation is now a common and viable treatment for these lesions throughout the UK.
5.A 67-year-old known alcoholic man with acute onset neurological symptoms has beenreferred for an urgent CT brain to exclude haemorrhage. CT shows an isodense subdural onthe right, but the history’ of trauma was 24 hours earlier with no previous history of head
injury or fall. All of the following are causes of isodense subdural hacmatoma on CT following head trauma, except
A. A 2-week-old head injury with subdural haemorrhage
B. Acute subdural haematoma in a patient with Hb 7.5 g/dL
C. Chronic haematoma in a patient with coagulopathy
D. Patient with an associated arachnoid tear
E. Patient with leptomeningeal metastasis
CT attenuation of blood in the subdural space remains denser than brain for 1 week and is less dense after 3 weeks. There is an interim period of 2 weeks when it is isodense to brain tissue.
In addition to variation in appearance over time, subdural haemorrhage may have a variable appearance in a setting of systemic disease like anaemia and coagulopathy.
An acute SDH can appear isodense in the following settings: anaemia with a haemoglobin concentration of <10 g/dL, admixture of CSF in the subdural space caused by an associated tear to the arachnoid layer and disseminated intravascular coagulation.
If there is chronic CSF leakage of venous blood, for example, if the patient has coagulopathy or is on anticoagulants/antiplatelet agents, chronic haematoma may look isodense rather than hypodense.
Meningeal metastasis may appear as hyperdensity on gvri and mimic subarachnoid haemorrhage
A. Ileoileal
B. Ileocolic
C. Ileoileocolic
D. Colocolic
E. Jejunoileal
Intussusception is one of the most common causes of acute abdomen in infancy. Intussusception occurs when a portion of the digestive tract becomes telescoped into the adjacent bowel segment. This condition usually occurs in children between 6 months and 2 years of age. In this age group, intussusception is idiopathic in almost all cases. The vast majority of childhood cases of intussusception arc ileocolic.
US is highly accurate in the diagnosis of intussusception with a sensitivity of 98% 100% and a specificity of 88%-100%. US is also good at demonstrating alternative pathology. Hence, enema could be reserved for therapeutic purposes when US is available.
A. Moyamoya disease
B. Takayasu arteritis
C. Churg-Strauss disease
D. PAN
E. Wegener’s granulomatosis
Takayasu arteritis is a form of granulomatous vasculitis affecting large and medium-sized arteries, characterised by ocular disturbances and weak pulses in the upper extremities (pulseless disease).
It is associated with fibrous thickening of the aortic arch with narrowing of the origins of the great vessels at the arch. Takayasu arteritis can be limited to the descending thoracic and abdominal aorta. It is seen in young and middle-aged patients, especially Asian and women. The diagnosis is confirmed by a characteristic arteriographic pattern of irregular vessel walls, stenosis, post-stenotic dilatation, aneurysm formation, occlusion and evidence of increased collateral circulation.
Polyarteritis nodosa is a fibrinoid necrotising vasculitis that mainly involves small and mediumsized arteries of the muscles. Multiple aneurysm formation is a characteristic finding. The kidney is most commonly involved, followed by the GI tract, liver, spleen and pancreas. Positive ANCA titres (usually pANCA type) are found in variable percentages of patients.
Wegener s granulomatosis is a distinct clinicopathologic entity characterised by granulomatous vasculitis of the upper and lower respiratory tract together with glomerulonephritis.
Churg-Strauss syndrome is characterised by granulomatous vasculitis of multiple organ systems, particularly the lung, and involves both arteries and veins as well as pulmonary and systemic vessels.
Moyamoya disease is a progressive vasculopathy leading to stenosis of the main intracranial arteries. Characteristic angiographic features of the disease include stenosis or occlusion of the arteries of the circle of Willis, as well as the development of collateral vasculature that produces a typical angiographic image called clouds of smoke’ or ‘puff of cigarette smoke’.
@# 8. A slimly built 60-year-old woman presents with anorexia, diarrhoea, and weight loss. Barium meal shows multiple filling defects in the stomach with thickened gastric rugae. Colonoscopy shows multiple colonic polyps. The top differential is
A. Peutz-Jeghers syndrome
B. Familial adenomatous polyposis
C. Cronkhite-Canada syndrome
D. Cowden syndrome
E. Turcot’s syndrome
Cronkhite-Canada syndrome occurs in older patients with an average age of 60 with no familial predisposition.
The histologic appearance of the GI polyps resembles that of juvenile polyps, and they are characteristically distributed throughout the stomach.
They are commonly small, sessile and characterised by cystic dilatation of the glands and inflammation of the lamina propria.
Patients commonly present with abdominal pain, protein-losing diarrhoea, anorexia and weight loss. Dystrophic nail changes and alopecia usually appear after the onset of GI symptoms.
A. Cystosarcoma phylloides
B. Complex breast cyst
C. Invasive lobular carcinoma
D. Fat necrosis
E. Fibroadenoma
Fat necrosis is a frequently encountered cause of benign calcification, particularly when there is a history of trauma. It appears well circumscribed with translucent areas in the centre (homogenous fat density’ of the oil cyst). Occasionally, it shows curvilinear or eggshell calcification in the wall.
On US, it appears as a hypoechoic or anechoic mass with ill- or well-defined margins, with or without acoustic shadowing or as a complex cyst.
A. Pyogenic discitis
C. Degenerative disc disease with Modic Type II end plate changes
D. Pott disease
E. Vertebral lymphoma
Infection usually begins in the anterior part of the vertebral body adjacent to the end plate.
Subsequent demineralisation of the end plate results in loss of definition of its dense margins on conventional radiographs.
These end plate changes allow the spread of infection to the adjacent intervertebral disk, resulting in a classic pattern of involvement of more than one vertebral body together with the intervening disks.
It also allows spread into the paraspinal tissues, resulting in the formation of a paravertebral abscess. However, if there is anterior subligamentous involvement of the spine, infection can extend both superiorly and inferiorly, with sparing of the intervertebral disks.
A normal chest radiograph is present in up to 50% of cases. In the later stages of disease, there is often vertebral collapse with a gibbus deformity.
Tuberculosis rarely affects the posterior vertebral elements (including the pedicles), in contrast to metastatic disease.
Anterior scalloping seen with subligamentous spread of infection can also be seen with paravertebral lymphadenopathy, secondary to metastases or lymphoma.
In differentiating tuberculosis from pyogenic infection, the clinical picture is as important as the radiologic features, with insidious onset of symptoms, a normal erythrocyte sedimentation rate, relevant respiratory symptoms and slow disease progression favouring a diagnosis of tuberculosis.
Radiologic features that favour this diagnosis include involvement of one or more segments; a delay in destruction of the intervertebral disks; a large, calcified paravertebral mass; and the absence of sclerosis.
Sarcoidosis can produce multifocal lesions of vertebrae and disks, along with paraspinal masses that appear identical to tuberculosis.
A. Wilson disease
B. Huntington disease
C. MELAS
I). Hallervorden-Spatz disease
E. CADASIL
The ‘eye of the tiger sign represents marked low signal intensity of the globus palladi on T2-weighted MRI, surrounding a central, small hyperintense area. The sign is seen in what was once known as Hallervorden-Spatz (HS) syndrome but is now called neurodegeneration with brain iron accumulation (NBIA) or pantothenate kinase II (PANC2)-associated neurodegeneration.
The low signal is a result of excessive iron accumulation and the central high signal is attributed to gliosis, increased water content and neuronal loss with disintegration. Iron levels in blood and CSF are normal. HS is a neurodegenerative disorder associated with extrapyramidal dysfunction and dementia. The sign can also be seen in other extrapyramidal Parkinsonian disorders such as cortical-basal ganglionic degeneration, Steele-Richardson-Olszewski syndrome, and early onset levodopa-responsive Parkinsonism.
High signal in the basal ganglia, thalamus and midbrain is seen in Wilson disease.
Caudate is atrophic in Huntington disease.
CADASIL shows extensive white matter signal change
and MELAS shows multiple focal white matter signal changes.
A. Calcification is uncommon.
B. Well circumscribed.
C. Displaces major vessels rather than encasing them.
D. Encases major vessels but does not invade them.
E. Claw of renal tissue extends partially around the mass.
Neuroblastoma (NBL) is the most common extracranial tumour in childhood and commonly presents as an abdominal mass. Abdominal and pelvic tumours are usually large and heterogeneous, and approximately 80%-90% demonstrate calcification on CT scans. Low attenuation areas of necrosis or haemorrhage are frequently noted at CT. Vascular encasement and compression of the renal vessels, splenic vein, inferior vena cava, aorta, celiac artery and superior mesenteric artery may occur, and vascular invasion is rare. Regional invasion of the psoas and paraspinal musculature may occur, and invasion of the neural foramen into the epidural space is also frequent; these are better evaluated at MR imaging, as is regional organ invasion. Metastatic disease of the liver and lung are readily evaluated with CT. They are typically heterogeneous, variably enhancing and of relatively low signal intensity on T1 weighted images and high signal intensity on T2-weighted images.
Wilms tumour demonstrates a ‘daw’ of normal renal tissue around the tumour. In contrast to neuroblastoma, vessels are displaced rather than encased and vascular invasion occurs in approximately 5%-10% of cases.
A. Myocardial calcification
B. Right atrial calcification
C. Mitral annulus calcification
D. Calcified vegetations
E. Left ventricular aneurysm calcification
A cardiac false aneurysm is defined as a rupture of the myocardium that is contained by pericardial adhesion. It usually represents a rare complication of myocardial infarction, but it may also occur after cardiac surgery’, chest trauma and endocarditis. True left ventricular aneurysms are discrete, dyskinetic areas of the left ventricular wall with a broad neck. Unlike a true aneurysm, which contains some myocardial elements in its wall, the walls of a false aneurysm are composed of organised haematoma and pericardium only. Both demonstrate focal bulge to the cardiac contour and can calcify.
Marked delayed enhancement of the pericardium on dynamic enhanced MRI may help in differentiating a false aneurysm from a true one.
@# 14. A 70-year-old man presents with rectal bleeding. Flexible sigmoidoscopy shows a circumferential tumour in the upper third of the anal canal. An MRI performed for staging shows locoregional lymphadenopathy. The lymph node group most likely to be involved is
A. Superficial inguinal
B. Common iliac
C. Pudendal
D. External iliac
E. Paraortic
Metastatic spread to regional lymph nodes represents the most common mode of tumour spread from cancer of the anal canal and margin. Nodal metastasis is more likely in cases of larger tumour size or a poorly differentiated anal tumour. Metastasis most commonly occurs to the perirectal nodes, with inguinal nodal spread being the second most common location of nodal metastasis.
A. Cystosarcoma phylloides
B. Fibroadenoma
C. Complex breast cyst
D. Invasive lobular carcinoma
E. Fat necrosis
Fibroadenomas are the most common cause of benign solid mass in the breast. On US, they appear round or oval, wider than tall, hypoechoic, well-defined and mostly homogenous and show a ‘hump and dip’ sign (small focal bulge to the contour with a contagious small sulcus), a thin echogenic pseudocapsule and rarely cither posterior acoustic enhancement (17%-25%) or posterior acoustic shadow (9%—11%).
A. Parsonage Turner syndrome
B. Spinoglenoid notch paralabral cyst
C. Duchenne’s muscular dystrophy
D. Quadrilateral space syndrome
E. Acute rotator cuff tear
The anatomy of the suprascapular nerve renders it particularly susceptible to compression at the suprascapular notch and spinoglenoid notch.
The pattern of muscle denervation provides information about the duration of entrapment and can identify the site of neurologic compromise.
Acute denervation presents as hyperintensity of the supraspinatus and infraspinatus or of the infraspinatus muscle alone on fluid-sensitive sequences.
Chronic compression is shown as a reduction in muscle bulk and fatty infiltration of the involved muscles.
Involvement of both the supra- and infraspinatus muscles reflects proximal compression at the suprascapular notch,
whereas isolated infraspinatus denervation suggests compression at the spinoglenoid notch.
Quadrilateral space syndrome is a rare condition referring to an isolated compressive neuropathy of the axillary nerve. It generally results in isolated atrophy of the teres minor and, less commonly, of the deltoid, which appears as a reduction in muscle bulk and fatty infiltration with chronic compression.
Parsonage-Turner syndrome is an uncommon, self-limiting disorder characterised by sudden onset of non-traumatic shoulder pain associated with progressive weakness of the shoulder girdle musculature.
MR] is the technique of choice in patients with shoulder pain and weakness. It is sensitive for the detection of signal abnormalities in the shoulder girdle musculature related to denervation injury.
MRI is also useful in excluding intrinsic shoulder abnormalities that can produce symptoms similar to Parsonage-Turner syndrome such as rotator cuff tears, impingement syndrome and labral tears.
None of the findings or history would be compatible with an acute rotator cuff tear or Duchenne’s muscular dystrophy.
A. Sacral meningocoele
B. Sacral chordoma
C. Central dural ectasia
D. Rhabdomyosarcoma
E. Sacrococcygeal teratoma
A chordoma is a tumour that derives from notochordal remnants. At imaging, it typically manifests as a large, destructive sacral mass with secondary soft-tissue extension. Radiographs may show sacral osteolysis with an associated soft-tissue mass and calcifications. CT shows bone destruction with an associated lobulated midline soft-tissue mass. Areas of low attenuation within the mass reflect the myxoid properties (high water content) of the tissue. Areas of punctate calcification often are noted.
At MR imaging, the most striking feature is the high signal intensity seen on T2-weighted images. High T2 signal intensity is a non-specific feature; however, the combination of high T2 signal intensity and a lobulated sacral mass that contains areas of haemorrhage and calcification is strongly suggestive of a chordoma. Chordomas tend to show hypointense or isointense signal relative to that in muscle on T1-weighted images, and contrast-enhanced images show a modest degree of heterogeneous enhancement in the soft-tissue components of the tumour. Areas of intrinsic Tl signal hyperintensity typically represent areas of haemorrhage or mucinous material. The tumour may cross the sacroiliac joint.
A. Congenital lobar emphysema
B. Viral pneumonia
C. Cystic fibrosis
D. Pulmonary sequestration
E. Inhaled foreign body
Most inhaled foreign bodies are organic and may not be visible on chest X-ray. It is recognised that chest X-ray can be normal with inhaled foreign bodies and clinical suspicion needs to be high. The most common findings are unilateral, distal obstructive emphysema, followed by normal X-ray. Lower lobes are most commonly involved. Long-standing unrecognised foreign body may present with recurrent or non-resolving consolidation or unexplained segmental collapse.
A. Type I endoleak
B. Type II endoleak
C. Type III endoleak
D. Type IV endoleak
E. Type V endoleak
In a Type I endoleak, there is poor apposition between one of the attachment sites of a stent graft and the native aortic or iliac artery wall, and blood leaks through this defect into the aneurysm sac. A Type I endoleak can be seen immediately after stent-graft deployment On CT, dense contrast collection is usually seen centrally within the sac and is often continuous with one of the attachment sites.
Type 11 endoleaks are the most common. They occur when there is retrograde flow of blood into the aneurysm sac via an excluded aortic branch, most commonly IMA or a lumbar artery. Many Type II endoleaks close spontaneously over time. CT shows peripheral or central location of acute haemorrhage.
Leakage of blood through the body of a stent graft results in a Type III endoleak. Type III endoleaks manifest as collections of haemorrhage or contrast material centrally within the aneurysm sac, usually distant from the attachment sites or native vessels.
Opacification of the aneurysm sac immediately after placement of a stent graft without a discernible source of leakage is designated a Type IV endoleak.
A Type V endoleak, or endotension, is characterised by continued growth of an excluded aneurysm sac without direct radiologic evidence of a leak.
@# 20. A 76-year old woman with 6 months’ history of progressive weight loss and altered bowel habits is referred for a CT scan of the abdomen and pelvis. The examination shows several hypoattenuating lesions on Segments II and III of the liver that are highly suspicious for malignancy. Blood biochemistry with tumour markers shows a normal AFP and CA 19-9 but raised CEA. LFTs are minimally deranged. The case is discussed at MDT.
What is the most likely differential diagnosis and further management plan out of the options given?
A. Primary hepatocellular carcinoma - liver biopsy
B. Hepatic adenoma - liver resection
C. Probable lung cancer - CT chest
D. Metastatic renal carcinoma - renal biopsy
E. Metastasis from colonic adenocarcinoma colonoscopy
A. Rim enhancement is a non-specific finding.
B. Fat content is a sign of benignity.
C. Homogenous enhancement is a sign of benignity.
D. Centripetal spread of contrast is more common in carcinomas.
E. Homogenous high T2 signal suggests malignancy.
Smooth margins, characterised by well-defined and sharply demarcated borders, are the feature with the highest benign lesion predictive value. Round and oval shapes have also been found to be predictive of benignity.
Homogeneous enhancement is highly suggestive of benign nature.
Fat content is specific to benign lesions, such as hamartoma, fibroadenoma, intramammary lymph nodes or fat necrosis.
In the case of fat necrosis, even if the lesion appears irregular in both shape and margin, with rim enhancement, the key to diagnosis is a fat internal signal on unenhanced sequences without fat suppression.
Strong hypersignal on non fat suppressed T2-weighted sequences is classically considered to be a clear sign of fibroadenoma, but it is non-specific and is seen in mucinous carcinomas, invasive ductal carcinomas, metaplastic carcinomas and intracystic papillary carcinomas (although it does not have a homogenously high T2 signal as fibroadenoma).
Although rim enhancement is regarded as suggestive of malignancy, a regular enhanced rim, which may be thick, may be seen around cysts, seroma (both of which are high T2 fluid signal) and fat necrosis (high T1 signal).
In relation to enhancement kinematics, a centrifugal contrast uptake pattern may help in diagnosing a fibroadenoma, whereas a centripetal spread of contrast is more common in carcinomas.
@# 22. Which statement is not associated with transient patellar dislocation?
A. The medial patellar retinaculum frequently demonstrates high T2W signal changes.
B. A tibial tuberosity to trochlear groove distance of <1.5 cm.
C. Trochlear dysplasia is a predisposing condition.
D. There is an increase in the ratio of the patellar tendon to the patellar length.
E. Bone contusions of the anterolateral aspect of the lateral femoral condyle.
Transient patellar dislocation is the dislocation of the patella laterally and subsequent relocation.
Trochlear dysplasia, patella alta (increase in the ratio of the patella tendon to the patella length) and an increase in the tibial tuberosity trochlear groove (TT-TG) distance are associated factors.
TT-TG >20 mm is abnormal and 15-20 mm is considered borderline change.
TT-TG less than 15 mm is within normal limits.
Contusional marrow oedema is often seen in the medial patellar facet and the lateral femoral condyle.
The medial patellar retinaculum and/or medial patellofemoral ligament (MPFL) may be torn or show a pattern of strain injury.
A. Modic Type I end plate change
B. Modic Type II end plate change
C. Andersson lesion
D. Modic Type III end plate change
E. Discitis
Modic described three types of reactive changes in the cancellous bone adjacent to the vertebral end plates.
Type I change is low on Tl and high on T2, representing oedema secondary to acute fibrovascular tissue invasion.
Type 2 change represents fatty replacement of red marrow, bright on Tl and T2. This leads to bony sclerosis, low on Tl and T2.
Occasionally the end plates become irregular and the degenerative process progresses to a destructive discovertebral lesion, simulating infective discitis. The key differentiation is signal of the disc, which is high in discitis and low in degeneration.
Andersson lesions refer to inflammatory involvement of the intervertebral discs by spondyloarthritis.
A. Atlanto axial distance <5 mm
B. Displacement of 6 mm of the lateral masses relative to the dens
C. Absence of lordosis
D. Disruption of the spinolamellar line
E. Anterior subluxation of C2 on C3
The atlantoaxial interval is defined as the distance between the anterior aspect of the dens and the posterior aspect of the anterior ring of the atlas. This distance should be 5 mm or less. Pseudospread of the atlas on the axis (‘pseudo-Jefferson fracture’) can be seen on anterior open-mouth radiographs. Up to 6 mm of displacement of the lateral masses relative to the dens is common in patients up to 4 years old and may be seen in patients up to 7 years old. On extension radiographs, overriding of the anterior arch of the atlas onto the odontoid process can be seen in 20% of healthy children.
In children, the C2-3 space and, to a lesser extent, the C3-4 space have a normal physiologic displacement. The absence of lordosis, although potentially pathologic in an adult, can be seen in children up to 16 years of age when the neck is in a neutral position.
In children, the flexion manoeuvre can increase the distance between the tips of the C1 and C2 spinous processes. Normal posterior intraspinous distance is a good indicator of ligamentous integrity and should not be more than 1.5 times greater than the intraspinous distance one level either above or below the level in question. Anterior wedging of up to 3 mm of the vertebral bodies should not be confused with compression fracture. Such wedging can be profound at the C3 level.
A prevertebral space of less than 6 mm at the level of C3 is considered normal in children.
In paediatric patients, widening of the prevertebral soft tissues can be a normal finding that is related to expiration.
Disruption of the spinolamellar line is a sign of injury.