TEST PAPER 7 Flashcards
(120 cards)
1.A middle-aged patient who sustained RTC 6 months ago presents with progressive visual lossand exophthalmos on the right. MRI demonstrated a dilated superior ophthalmic vein withflow voids in the cavernous sinus. What is the likely diagnosis?
A. Buphthalmos
B. Carotid-cavernous fistula
C. Orbital pseudotumour
D. Arteriovenous malformation
E. Dural fistula
1.B. Carotid-cavernous fistula
Carotid-cavernous fistula (also described as caroticocavernous fistula) is an abnormalcommunication between the internal carotid artery (ICA) and the veins of the cavernous sinus.
It is mostly due to trauma with laceration of the ICA within the cavernous sinus usually due to a skull base fracture or penetrating trauma. Ultrasound and MRI usually show arterial flow in the cavernous sinus and superior ophthalmic vein.
2.A preterm neonate on the intensive care unit develops gross abdominal distension andbleeding per rectum. A supine abdominal radiograph is performed demonstrating multipleloops of dilated bowel loops.
Given the likely diagnosis, all of the following would be expected findings on the supine radiograph, except:
A. Mottled gas shadows within the bowel wall
B. Branching gas pattern overlying the liver shadow
C. Foci of calcification projected over the renal angles
D. Generalised lucency overlying the liver shadow
E. Rounded area of lucency within the central abdomen
2.C. Foci of calcification projected over the renal angles
The main observations to be made on the plain abdominal radiograph relate primarily to thepresence, amount and distribution of gas, which includes intraluminal gas, intramural gas, portal venous gas and free intraperitoneal gas. From observations of the intraluminal gas, it may sometimes be possible to make inferences regarding the presence of bowel wall thickening, free fluid and focal fluid collections.
Dilatation with loss of the mosaic pattern and the development of rounded or elongated loops is more suggestive that an abnormality is present. On plain abdominal radiographs, intramural gas may be diffuse or localised and appears as linear or rounded radiolucencies. Extensive intramural gas can result in a mosaic pattern or bubbly appearance. Portal venous gas appears as branching, linear, radiolucent vessels that may extend from the region of the main portal vein towards the periphery of both hepatic lobes.
On the supine view, large amounts of gas may give rise to the ‘football’ sign, where the gas outlines the whole of the peritoneal cavity, the undersurface of the diaphragm and the falciform ligament (the lacing of the football). In this view, even smaller amounts of free gas may be detected when both sides of the bowel wall are outlined (Rigler’s sign).
3.Which of the following is a recognised cause of a ‘bone within bone’ appearance?
A. Renal osteodystrophy
B. Paget’s disease
C. Hyperparathyroidism
D. Melorheostosis
E. Osteopathia striata
3.B. Paget’s disease
A ‘bone within bone’ appearance describes the radiographic appearance whereby a bone appearsto have another bone within it, which results from endosteal new bone formation. Recognised causes include Paget’s disease, sickle cell disease, thalassemia, Gaucher’s disease, acromegaly, hypervitaminosis D, scurvy and rickets, among many others. It can also be a normal finding in infants, particularly in the thoracolumbar spine.
4.A 25-year-old woman with recurrent urinary tract infections and post-void dribbling attendsthe urology clinic. The urologist suspects a urethral diverticulum. What is the mostappropriate first-line test?
A. Micturating cystourethrogram
B. Urodynamics
C. Transvaginal ultrasound
D. Double balloon catheter positive pressure urethrography
F. Pre- and post void magnetic resonance imaging of urethra
4.E. Pre- and post-void magnetic resonance imaging of urethra
Female urethral diverticula are thought to be caused by obstruction of Skene’s glands. Rarely,carcinoma (usually adenocarcinoma) or calculi can form within them. The gold standard imaging investigation is double-balloon catheter positive pressure urethrography; however, this is invasive and uses ionising radiation. The best first-line test is a pre- and post void magnetic resonance imaging (MRI) of the urethra, as this avoids ionising radiation and does not involve invasive placement of catheters, and the patient can empty her bladder in private between scans. Positive pressure urethrography is reserved for cases where MRI is equivocal. The remaining options are inappropriate: transvaginal ultrasound may show a lesion but will not clearly demonstrate its relationship to the urethra; micturating cystourethrogram would have a high likelihood of a false negative, requires catheterisation, uses ionising radiation and requires the patient to void in the presence of the radiologist; urodynamics are a functional examination.
5.A 40-year-old male and intravenous drug user, is on your barium list. The history on the cardsays ‘c/o dysphagia. Exclude pouch!’. During the barium swallow, you notice no oesophagealpouch but there are at least three giant 3- to 4 cm flat ulcers noted within the oesophagus near the gastro-oesophageal junction. The intervening oesophagus appears normal. Which of the following is the most likely diagnosis?
A. Cytomegalovirus oesophagitis
B. Caustic oesophagitis
C. Candida oesophagitis
D. Behcet’s disease
E. Crohn’s disease
- A. Cytomegalovirus oesophagitis
Cytomegalovirus oesophagitis almost always occurs exclusively in human immunodeficiency virus (HIV)-positive patients. Barium swallow or endoscopy appearances are of giant ovoid flat ulcers >2 cm near the gastro-oesophageal junction or less commonly, smaller superficial ulcers. Giant ulcers can also be seen in HIV at the time of seroconversion. Caustic ingestion would usually have a different clinical history and tends to produce stricture of the oesophagus. Candida tends to involve the upper oesophagus, has linear plaques and is associated with abnormal motility. Behcet’s disease (a rare immune-mediated systemic vasculitis) produces aphthous ulcers. Crohn’s disease rarely affects the oesophagus and also would produce aphthous ulcers.
- A 16-year-old girl with a history of recurrent bronchitis undergoes chest X ray. The lungs are clear but there is tracheal deviation to the left, with a focal indentation of the right wall of the trachea. Underlying vascular anomaly is suspected, and the patient undergoes a magnetic resonance imaging scan for further evaluation. All of the following will explain the above Chest X-ray appearance, except:
A. Double aortic arch
B. Right aortic arch with aberrant left subclavian artery and patent ductus arteriosus
C. Aberrant left pulmonary artery
D. heft aortic arch with aberrant right subclavian artery and patent ductus arteriosus
E. Common origin of innominate and left common carotid artery
- C. Aberrant left pulmonary artery
Double aortic arch variants and right aortic arch with aberrant left subclavian artery and patent ductus arteriosus are the two most common types of vascular rings which encircle the mediastinal airways. Both these conditions cause leftward deviation of the trachea and indentation of the right tracheal wall visible on the chest X-ray together with a large posterior oesophageal impression visible on oesophagogram. Left aortic arch with aberrant right subclavian artery is the most common vascular anomaly of the aortic arch, but only in the extremely rare association with patent ductus arteriosus will it cause similar appearances.
A less common vascular anomaly, which may cause a similar appearance of the trachea but does not cause any oesophageal indentation, is a common origin of innominate and left common carotid artery. Aberrant left pulmonary artery’ causes posterior tracheal indentation and anterior oesophageal impression.
- A 50 year-old man was recently diagnosed with a thyroid cancer following an ultrasound guided FNA of a thyroid lesion. Regarding malignant thyroid nodules, which of die following statements is true?
A. Punctate calcification is a feature of papillary carcinoma.
B. Anaplastic carcinoma is associated with MEN syndrome.
C. Echogenic foci seen in medullary carcinoma are due to calcitonin deposits.
D. Characteristic lymphadenopathy in medullary carcinoma is hypoechoic to muscle.
E. Follicular carcinoma can he differentiated from follicular adenoma on US.
- A. Punctate calcification is a feature of papillary carcinoma.
Thyroid calcifications may occur in both benign and malignant diseases. Thyroid calcifications can be classified as microcalcification, coarse calcification or peripheral calcification. Microcalcifications are found in 29%-59% of all primary thyroid carcinomas, most commonly in papillary thyroid carcinoma. Their occurrence has been described in follicular and anaplastic
thyroid carcinomas as well as in benign conditions such as follicular adenoma and Hashimoto’s thyroiditis.
At US imaging, microcalcifications appear as punctate hyperechoic foci without acoustic shadowing. Coarse calcifications may coexist with microcalcifications in papillary cancers, and they are the most common type of calcification in medullary thyroid carcinomas. Inspissated colloid calcifications in benign thyroid lesions may mimic microcalcifications in thyroid malignancies, but the former can be distinguished from malignant calcifications by the observation of ring-down or reverberation artefact. Peripheral calcification is one of the patterns most commonly seen in a multinodular thyroid but may also be seen in malignancy.
US features that should arouse suspicion about lymph node metastases include a rounded bulging shape, increased size, replaced fatty hilum, irregular margins, heterogeneous echotexture, calcifications, cystic area and vascularity throughout the lymph node instead of normal central hilar vessels at Doppler imaging.
- A 6-year-old boy presents with a 1-month history of progressive left-sided proptosis. An orbital MRI reveals a large, lobulated, retro-orbital mass without any intracranial or globe invasion. The mass is isointense to muscle on Tl and hyperintense on T2 with uniform enhancement post-contrast. The patient is afebrile, and inflammatory markers are not significantly raised. What is the most likely diagnosis?
A. Dermoid cyst
B. Orbital cellulitis with abscess formation
C. Lymphangioma
D. Capillary’ haemangioma
E. Rhabdomyosarcoma
- E. Rhabdomyosarcoma
Rhabdomyosarcoma is the most common mesenchymal tumour in children. Rhabdomyosarcoma is an aggressive, rapidly growing tumour and most often manifests with rapidly progressive proptosis or globe displacement. Orbital cellulitis is differential, but patients are afebrile and inflammatory markers are normal. On CT images, orbital rhabdomyosarcoma generally appears as an extraconal, irregular ovoid, well-circumscribed, homogeneous mass that is isoattenuated relative to muscle. Calcification is usually seen only in association with bone destruction. At MRI, they are isointense to muscle or brain with T1-weighted sequences and variably hyperintense to muscle and brain with T2-weighted pulse sequences. They enhance uniformly with contrast.
Dermoid cyst is the most common orbital mass in children. Imaging features that suggest a dermoid include a cystic appearance, internal fat attenuation or signal intensity (T1 hyperintensity) and internal calcification, all of which are uncommon in rhabdomyosarcoma.
On images, vascular malformations are often cystic and multiloculated with ill-defined borders. They frequently contain fluid-fluid levels because of haemorrhage into the cysts, whereas fluid fluid levels are quite uncommon in rhabdomyosarcoma. Peripheral enhancement can be seen around cystic area, which is uncommon in rhabdomyosarcomas.
- A 30-year-old woman was involved in a severe road traffic accident and sustained direct high-energy trauma to her pelvis. Among other injuries, she was found to have a fracture on her left sacroiliac joint and left ischiopubic ramus. What type of fracture has she sustained?
A. Open book
B. Straddle
C. Bucket handle
D. Duverney
E. Malgaigne
- E. Malgaigne
Pelvic fractures can be divided into stable and unstable fractures. The Malgaigne, open book, straddle and bucket-handle fractures are all unstable, as the pelvic ring is interrupted in two places. The Malgaigne fracture is described in this case. The open book fracture implies fracture/ diastasis of both ischiopubic rami and sacroiliac joints, the straddle fracture involves both obturator rings and the bucket-handle fracture refers to an SI joint fracture with a contralateral ischiopubic ramus fracture. Patients with unstable fractures are at significant risk of pelvic organ injury and haemorrhage. Duverney fracture is an isolated fracture of the iliac wing and is a stable fracture.
- A patient undergoes a routine abdominal ultrasound for generalised abdominal pain.
Unfortunately, the spleen cannot be detected. Which of the following is the least likely cause for this?
A. Myelofibrosis
B. Sickle cell anaemia
C. Polysplenia syndrome
D. Traumatic fragmentation of the spleen
E. Wandering spleen
- A. Myelofibrosis
Myelofibrosis causes splenomegaly and therefore make splenic detection easier. All of the other options provided are potential causes of a non-visualised spleen. Polysplenia syndrome (also known as bilateral left-sidedness) is, as the name suggests, actually associated with multiple spleens, but these are usually in the wrong place (in addition to a vast array of other intra-abdominal anomalies). A wandering spleen relates to the condition where the spleen is attached to an abnormally long and mobile pedicle, which means that the spleen can be found in places other than in the left upper quadrant
- A 6-year-old boy presents with adrenal insufficiency and developmental delay. Magnetic resonance imaging demonstrates diffuse T2 hyperintensity in the deep white matter, most predominant in the posterior parieto-occipital region and splenium of the corpus callosum. Which of the following is the most likely cause for this finding?
A. Metachromatic leukodystrophy
B. Acute disseminated encephalomyelitis
C. X-linked adrenoleukodystrophy
D. Alexander disease
F. Canavan disease
- C. X-linked adrenoleukodystrophy
Dysmyelinating diseases, or leukodystrophies, encompass a wide spectrum of inherited neurodegenerative disorders affecting the integrity of myelin in the brain and peripheral nerves. Most of these disorders fall into one of three categories lysosomal storage diseases, peroxisomal disorders and diseases caused by mitochondrial dysfunction - and each leukodystrophy has distinctive clinical, biochemical, pathological and radiological features. X-linked adrenoleukodystrophy is an inherited white matter disorder caused by gene mutation (ALD gene) resulting in abnormal formation of myelin. The childhood cerebral form (CCALD) is the mast common and affects males aged between 4 and 10 years. Hyperpigmentation can occur as a result of adrenal insufficiency. The diagnostic clue is symmetric, peritrigonal white matter abnormality involving the splenium. Alexander disease characteristically involves the frontal white matter preferentially, and Canavan disease causes diffuse white matter abnormality.
- A 26-year-old woman who had an intrauterine contraceptive device (IUCD) coil inserted 6 years ago presents to her general practitioner complaining of right iliac fossa pain, constipation, night sweats and fevers. The practitioner refers her for a transvaginal ultrasound, which shows a right-sided convoluted cobra-shaped structure containing fluid echogenicity and some polypoidal outgrowths from the wall. Adjacent to this is
a cystic left adnexal mass containing internal echoes. Which of the following is the likely diagnosis?
A. Actinomycosis
B. Appendix abscess
C. Diverticulitis with pericolic abscess
D. Migrated IUCD causing hydroureter
E. Salpingitis secondary to tuberculosis
- A. Actinomycosis
Pelvic actinomycosis is a rare chronic bacterial infection but is commonly seen in the setting of a long-standing IUCD. It can also be associated with recent surgery. It often causes abdominal pain, low grade fever and an abdominal or pelvic mass/abscess, which can mimic a malignant mass as it can get quite large if left untreated. The earlier it is diagnosed and treated, the less likely the patient will require surgery. The cobra-shaped structure is an infected dilated tube. Endometriosis can give cysts containing low-level echoes but fever would be unusual with pain. Appendix and diverticulitis can cause irritation of the adjacent tube but the clue is the long-standing IUCD.
- A 75-year-old man had a history of dyspnoea associated with haemoptysis and weight loss. Computed tomography (CT) showed a 1.5 cm spiculated mass in the anterior segment of the right upper lobe, 5 cm deep to the pleural surface on a background of widespread emphysematous change. The case was referred for discussion at multidisciplinary team meeting to consider safety of undergoing a CT-guided lung biopsy. In this patient’s case, which of the following statements concerning CT-guided lung biopsy is correct?
A. The patient carries a 10%-15% risk of developing pneumothorax.
B. As the lesion is not contiguous with the pleural surface, there is a lower risk of pneumothorax.
C. The patient carries an increased risk of developing pulmonary haemorrhage post-procedure.
D. If a pneumothorax were to develop as a complication, he is less likely to require subsequent intercostal drain insertion.
E. The procedure is relatively contraindicated because pulmonary function tests revealed a forced expiratory volume in 1 second (FEV1) of 45% predicted
- C. This patient carries an increased risk of developing pulmonary haemorrhage
post-procedure.
Studies have identified lesion depth as being the most important risk factor for pulmonary haemorrhage, with an increased risk in lesions deeper than 2 cm. The incidence of pneumothorax is reported to be between 22% and 45%, of which 3.3-15% will require a chest drain. The risk of developing pneumothorax increases significantly if the lesion is not contiguous with the pleural surface. Studies have shown that the presence of chronic obstructive airway disease increases the necessity of chest drain insertion, although this does not necessarily hold for risk of pneumothorax. Although there are no definite absolute contraindications to CT guided lung biopsy, there are, however, several relative contraindications. Patients should not undergo the procedure without adequate prebiopsy assessment or if they plan to fly within 6 weeks of the procedure. The risk is increased by abnormalities of lung function, respiratory failure (including mechanical ventilation), arterial and venous pulmonary hypertension and coagulation abnormalities. The balance of benefit against risk for the procedure should be assessed at a multidisciplinary meeting. Previous contralateral pneumonectomy precludes needle biopsy; however, if the lesion abuts the pleural surface and can be accessed with no needle traversing lung tissue, then the risk of pneumothorax is very low and may not, therefore, be considered as a contraindication. Patients should not undergo needle biopsy without further multidisciplinary team assessment if pulmonary function tests demonstrate an FEV1 of <35%.
- A 58-year-old man, who underwent coronary artery bypass grafting 8 years ago, presents to the cardiology clinic with symptoms of progressive shortness of breath on exertion, associated with increase in abdominal girth and peripheral oedema. Clinical examination elicits raised jugular venous pressure, with bibasal fine inspiratory crackles, shifting dullness and bilateral ankle pitting oedema. Elective ECG-gated spin-echo cardiac MRI demonstrates limited ability of the right ventricle to distend during filling (diastole), assuming a tubular shape, with limited change in cavity size during the end-systolic phase. Pericardial thickening of 6 mm and calcification is evident, with a moderate pericardial effusion and dilated superior vena cava and azygos vein. Which of the following is the most likely diagnosis?
A. Cardiac tamponade
B. Restrictive cardiomyopathy
C. Constrictive pericarditis
D. Dressier syndrome
E. Hypertrophic cardiomyopathy
- C. Constrictive pericarditis
Constrictive pericarditis is a recognised complication of cardiac surgery, with recent evidence showing an incidence of 0.2%. The most common cause, however, would be idiopathic, thought to result from an occult viral pericarditis, with tuberculosis being the most common cause worldwide. Clinical symptoms attributed to both left- and right-sided heart failure are usually present.
The hallmarks of pericardial constriction are pericardial thickening, pericardial calcification and abnormal diastolic ventricular function. Other findings associated with raised right-sided pressure such as dilatation of the superior vena cava and azygos vein help support the diagnosis. Constrictive pericarditis can be distinguished from restrictive cardiomyopathy on the basis of pericardial thickness measuring more than 4 mm in the presence of characteristic haemodynamic findings.
Dressier syndrome typically occurs 3 weeks to several months, not years, after cardiac surgery.
- An 8-month-old boy presents with a right upper quadrant mass. Blood results reveal a raised alpha fetoprotein (AFP). Ultrasound of the abdomen demonstrates a large 7-cm, hypervascular, heterogeneous hyperechoic mass in the liver with a few cystic regions.
There is no vascular invasion. No renal or suprarenal lesions are present. Which of the following differential diagnoses is most likely?
A. Hepatoblastoma
B. Infantile haemangioendothelioma
C. Hepatic haemangioma
D. Mesenchymal hamartoma of the liver
E. Fibrolamcllar hepatocellular carcinoma
- A. Hepatoblastoma
Hepatoblastoma is the most common primary hepatic tumour in children. Hepatoblastoma has been associated with several syndromes, including Beckwith-Wiedemann syndrome,
Gardner syndrome, familial adenomatous polyposis, type 1A glycogen storage disease and trisomy 18.
Hepatoblastomas are most often hyperechoic relative to adjacent liver on US. A spoke-wheel appearance with areas of alternating echogenicity may be seen at antenatal imaging. CT shows a sharply circumscribed mass that is slightly hypoattenuating relative to the adjacent liver on unenhanced and contrast-enhanced images. Epithelial hepatoblastomas demonstrate a more homogeneous appearance, while mixed tumours are more heterogeneous in attenuation. Speckled or amorphous calcification is seen in more than 50% of lesions. The tumour enhances slightly, but less than adjacent liver.
At MR imaging, epithelial hepatoblastomas are homogeneously slightly hypointense on T1-weighted images and hyperintense on T2-weighted images relative to adjacent liver parenchyma. Mixed tumours demonstrate more heterogeneous signal intensity characteristics. Fibrotic septa are hypointense on both Tl- and T2-weighted images and enhance after intravenous administration of gadolinium contrast material.
Infantile haemangioendothelioma (IHE) is a vascular tumour and enhances much more than adjacent liver, while hepatoblastoma typically enhances much less than adjacent liver. Occasionally, the peripheral rim enhancement on arterial phase images seen in hepatoblastoma may suggest IHE, but IHE is distinguished by intense nodular or corrugated peripheral enhancement with centripetal fill-in on delayed phase images. Mesenchymal hamartoma of the liver (MHL) is a benign tumour that manifests in the same age group as hepatoblastoma. It can usually be distinguished from hepatoblastoma by normal serum AFP levels in MHL, predominantly cystic appearance and age at diagnosis >5 years (cf. hepatoblastoma generally diagnosed <5 years).
- What is the purpose of the heel-toe manoeuvre in ultrasound examination of the shoulder?
A. To decrease the beam angle incidence
B. To minimise anisotropy
C. To increase the field of view
D. To minimise posterior reverberation artefact
E. To minimise beam width artefact
- B. To minimise anisotropy
The purpose of the heel-toe manoeuvre in ultrasound is the same in all situations regardless of the site being imaged. It is to reduce anisotropy artefacts that result when the probe is not perpendicular to the structure being imaged. Similarly, reducing beam angle incidence would increase such artefacts. Reducing probe compression reduces posterior reverberation artefact. Placing the structure of interest within the central region of the probe and placing the focal zone at the region of interest reduce beam width artefact.
- A 23-year-old woman presents with left iliac fossa pain. The uterus and both ovaries are within normal limits. There is an anechoic left adnexal cyst adjacent to the uterus that appears separate from the ovary. You note that the patient has had a previous ultrasound for left adnexal pain, and that a left adnexal cyst with similar dimensions was noted then. Which of the following is the most likely diagnosis?
A. Theca lutein cyst
B. Paraovarian cyst
C. Endometrioma
D. Adenomyosis
E. Dermoid cyst
- B. Paraovarian cyst
Paraovarian cysts arc responsible for about 10% of adnexal masses. They do not usually change in size. They are susceptible to torsion or bleeding which can cause pain but are usually asymptomatic. They are congenital, occurring from embryonic Wolffian or mesonephric duct remnants within the broad ligament, and are separate from the ovary. Theca lutein cysts are usually bilateral.
Endometriomas usually contain low-level echoes and there is often more than one deposit; they are also less likely to remain static over time. Adenomyosis is a uterine abnormality that involves abnormal glandular tissue within the myometrium and causes thickening of the myometrium.
An ovarian dermoid would usually be hyperechoic or contain mixed elements, giving it a heterogeneous appearance.
- A patient undergoes pancreatic transplantation. Which of the following statements is least likely?
A. The transplanted pancreatic duct is normally dilated.
B. Indistinct pancreatic margins on ultrasound may indicate graft rejection.
C. Most patients have a simultaneous renal transplant
D. The donor pancreas is normally grafted onto the external iliac vessels.
E. Most patients achieve insulin independence
- A. The transplanted pancreatic duct is normally dilated.
Pancreatic transplant is a potentially curative treatment option predominantly for Type 1 diabetes. The pancreas is normally grafted onto the external iliac vessels. In most cases, the procedure is combined with a simultaneous renal transplant. Exocrine pancreatic secretions can be redirected either into the bladder (easier with simultaneous renal transplant) or bowel. There are advantages and disadvantages of both approaches; redirection to the bladder enables close monitoring of secretions but can lead to acidosis. Radiological input is usually required in postoperative monitoring. Ultrasound scanning can reveal peripancreatic collections/pseudocysts, vessel thrombosis and other signs of acute rejection (indistinct pancreatic margins, acoustic inhomogeneity of the pancreas and dilatation of the pancreatic duct).
- A 30-year-old woman presents with bilateral foot drop 2 days post-partum. What finding on MRI would explain this?
A. Posterior disc protrusion at L3/L4
B. Bilateral common peroneal nerve entrapment
C. Bilateral sciatic nerve compression
D. Paracentral disc protrusion at L3/L4
E. Spinal canal stenosis at L3/L4
- B. Bilateral common peroneal nerve entrapment
Common peroneal neuropathy (CPN) is the most common mononeuropathy in the lower extremity. In most cases, CPN neuropathy occurs in the knee region, whereas neuropathy of the superficial peroneal nerve (SPN) and deep peroneal nerve (DPN) occurs more distally in the leg, ankle or foot.
The CPN is particularly prone to entrapment because it is fixed in position at the greater sciatic foramen (peroneal division) and around the fibular head. There are two common compression sites of the CPN. The nerve may be compressed as it crosses the fibular neck, owing to its superficial location, or as it travels under the origin of the peroneus longus muscle. Injury to the nerve at these locations may be the result of extrinsic compression, stretch injury or direct trauma.
Extrinsic compression of the CPN can be the result of external compression by various agents such as short-leg cast, crush injury, surgery, tumour, osteochondroma, synovial cyst, intraneural
and extraneural ganglia, varicosities, aberrant muscle, prolonged immobilisation (Saturday night palsy), prolonged squatting (strawberry pickers’ palsy) and extended lithotomy position due to childbirth or obstetric surgery will typically produce bilateral CPN entrapment. Diabetic patients are at an increased risk for entrapment of the CPN within the fibrous tunnel underneath the peroneus longus muscle.
Patients with CPN often present with frequent tripping related to a foot drop. Pain may be present at the site of compression. Sensory disturbances include paraesthesia and anaesthesia along the lateral lower leg and dorsal foot. On physical examination, patients demonstrate foot drop, weak foot extension (anterior tibial muscle), weak foot eversion (peroneus longus and brevis muscles) and loss of sensation in the lower lateral two-thirds of the leg and the dorsum of the foot.
- On an antenatal ultrasound, a foetus is found to have an intracranial anomaly. At birth, the cranial ultrasound reveals a large cystic mass in the posterior fossa communicating with the fourth ventricle with hypoplasia of the cerebellar vermis.
What other associated abnormality would you not expect to be associated with the underlying condition?
A. Subependymal calcification
B. Corpus callosum agenesis
C. Grey matter heterotopia
D. Schizencephaly
E. Occipital encephalocoele
- A. Subependymal calcification
Dandy-Walker malformation is the most common posterior fossa malformation. The key neuroimaging features are hypoplasia (or, rarely, agenesis) of the cerebellar vermis (whose inferior portion is typically affected, possibly in combination with its superior portion), which is elevated and upwardly rotated; and dilatation of the cystic-appearing fourth ventricle, which consequently may fill the entire posterior fossa.
Additional malformations, including dysgenesis or agenesis of the corpus callosum, occipital encephalocele, polymicrogyria and grey matter heterotopia, may be present in 30% 50%. Hydrocephalus is associated in about 90% of patients.
Subependymal calcification is a feature of tuberous sclerosis.
- A 13-year-old boy presents with symptoms and radiographic evidence of a slipped capital femoral epiphysis (SCFE). It is noted on his radiographs that the physes are generally wide with flaring of the metaphyses. Which of the following is the most likely diagnosis?
A. Rickets
B. Hypophosphatasia
C. Blounts disease
D. Achondroplasia
E. Renal osteodystrophy
- A. Rickets
Rickets is the paediatric equivalent of osteomalacia. It affects the metaphysis of hones as these are the most metabolically active sites. Common sites of involvement include proximal humerus, proximal tibia and proximal and distal femur. Appearances include widened and irregularly shaped physeal lucencies and metaphyseal flaring. There may be long bone deformation with lower limb bowing. Patients with rickets are at increased risk of Salter-Harris I fractures of the epiphyses that most commonly occur at the proximal femur (SCFE).
While Blount’s disease is often associated with bow legged-ness in infants and children, it is an abnormality at the knee with an increase in the tibial metaphyseal angle. There arc a few cases in the literature of SCFE in association with Blount’s disease.
While hypophosphatasia may give similar findings to rickets, its incidence 1:10 0000 is several orders of magnitude less than rickets (1:100-1:1000).
- A 76 year-old woman is having a pelvic magnetic resonance imaging (MRI) scan to assess for a possible hernia. She is noted to have a 6 cm very low intensity lesion within the right ovary on both Tl and T2. Some fluid is also noted within the pelvis. Which of the following is the most likely diagnosis?
A. Ovarian mucinous cystadenoma
B. Krukenberg tumour
C. Ovarian fibroma
D. Dermoid cyst
E. Clear cell carcinoma of the ovary
- C. Ovarian fibroma
Ovarian fibromas typically arise in postmenopausal women and are usually asymptomatic. Rarely, they can cause pressure-type symptoms if they get large enough, or tort causing pain.
Ovarian fibromas are classically known to cause Meigs syndrome, which is the combination of ascites, pleural effusion and a benign ovarian tumour. The ascites and pleural effusion often resolve after tumour removal. They are also more common in Gorlin (basal cell naevus) syndrome, where they tend to occur at a younger age and are more likely to be bilateral. Owing to their highly fibrous component, they have a similar intensity to uterine fibroids, being low on IT and T2-weighted sequences. On ultrasound, they are often hypoechoic with attenuation of the ultrasound beam as it passes through the lesion. About 1% can undergo malignant transformation to a fibrosarcoma.
Krukenberg tumours result from ovarian metastases, classically from the stomach; however, colon, breast, lung, gynaecological tumours, sarcomas and melanoma can also spread to the ovary.
These tumours would less likely be so low intensity on Tl and T2-weighted images and there may be a history of cancer. Ovarian mucinous cystadenomas tend to contain a jelly-like fluid, so are usually cystic on imaging, but can contain solid components. A dermoid cyst usually contains mixed elements including fat and would not usually cause ascites. Clear cell carcinoma is an aggressive ovarian lesion associated with endometriosis and a poor prognosis; these often have cystic and solid components.
- You are reviewing the X-rays of a 44-year-old male patient who has complained of mild breathlessness and a cough but otherwise well. Several chest radiographs performed over an 18 month period demonstrate diffuse ground glass shadowing with several scattered confluent areas of air-space consolidation. The lung changes do not appear
to have any zonal predilection, and no mediastinal, hilar or cardiac abnormality is evident. HRCT also showed fairly extensive smooth interlobular septal thickening.
The intervening lung appears normal, and there is sharp demarcation between the abnormal and normal lung parenchyma. Which of the following is most likely given the radiological findings described?
A. Pulmonary vasculitis
B. Pulmonary oedema
C. Primary tuberculosis
D. Alveolar proteinosis
E. Extrinsic allergic alveolitis
- D. Alveolar proteinosis
Alveolar proteinosis is a rare disorder that is characterised by the abnormal accumulation of proteinaceous material in alveoli, secondary to altered surfactant homeostasis. It affects young to middle-aged adults and is more common in men. There is a strong association with cigarette smoking. Clinical features are variable, with symptoms usually being of gradual onset. Chest radiography typically demonstrates bilateral air-space opacity with either an ill-defined nodular or ground glass pattern. An important discriminator from pulmonary oedema is the presence of perihilar lung changes in the absence of cardiomegaly, pulmonary venous hypertension and pleural effusions. Similarly, while sarcoidosis can mimic many lung conditions, the absence of lymphadenopathy is an important feature to note in alveolar proteinosis. The classic computed tomography finding is known as crazy paving - the description given to the combination of patchy ground-glass opacities with smooth interlobular septal thickening in a geographical distribution.
- An otherwise healthy 44-year-old patient presents acutely unwell with new-onset epigastric pain and is found to have a significantly raised amylase level. Which of the following clinical scenarios is least likely?
A. Alcoholic patient, recent 48-h binge
B. Previous bouts of right upper quadrant abdominal pain
C. Recent flu like symptoms
D. Computed tomography report describing a 6 cm pseudocyst
E. Fulminant haemolytic-uraemic syndrome
- D. Computed tomography report describing a 6 cm pseudocyst
The clinical scenario presented is that of new-onset acute pancreatitis. Pseudocysts are encapsulated collections of pancreatic fluid found in a peripancreatic position. Classically, these take 4 weeks to develop. The other options provided are all potential causes of acute pancreatitis. Alcoholism and cholelithiasis are the most common causes. Recent viral infection (e.g., mumps, hepatitis, glandular fever), trauma, structural anomalies (pancreas divisum), some drugs (e.g., steroids, azathioprine, diuretics) and multisystem conditions (shock, haemolytic-uraemic syndrome, systemic lupus erythematosus) are all recognised causes of pancreatitis. In a large number of patients, no definite cause is ever identified (idiopathic).