Radiology Spotters mixed Bag Collection for post graduates student .PPT
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Radiology Spotters collection by Dr Pradeep. nice collection of radiology spotter made by or collected by Dr. Pradeep, this is a collection of confusing spotter and very important spotter commonly asked in exams, our references is radiopaedia, learning radiology and Aunt Minnie.. Thanks.
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Radiology Spotters mixed Bag Collection for post graduates student .PPT
- 1. Spotter Radiology Spotter collection (MOST VVI ) Dr Pradeep
- 2. Persistent primitive trigeminal artery
- 4. Variant anatomy of the aortic arch
- 5. Right aortic arch with aberrant left subclavian artery
- 8. Aberrant right subclavian artery
- 10. Aberrant left pulmonary artery
- 11. Bovine arch is the most common variant of the aortic arch and occurs when the brachiocephalic (innominate) artery shares a common origin with the left common carotid artery
- 17. ELST
- 18. Ependymoma
- 19. Medulloblastoma
- 23. Ganglioglioma
- 25. Tuberous sclerosis or Bourneville disease
- 27. VHL
- 28. HIPPEL • H: haemangioblastoma • I: increased risk of renal cell cancer • P: phaeochromocytoma • P: pancreatic lesions (cyst, cystadenoma, cystadenocarcinoma) • E: eye dysfunction (retinal haemangioblastoma), endolymphatic sac tumours • L: liver, renal and pancreatic cysts
- 29. NF1 or von Recklinghausen disease, • CAFE SPOT • Mnemonic • C: café-au-lait spots (greater than six seen during one year) • A: axillary or inguinal freckling • F: fibromas (neurofibroma (two or more) or plexiform neurofibroma (one)) • E: eye hamartomas (Lisch nodules) • S: skeletal abnormalities, e.g. sphenoid wing dysplasia, leg bowing • P: positive family history • OT: optic tumour (optic nerve glioma)
- 30. NF2
- 31. Mnemonics • MISME • M: multiple • I: inherited • S: schwannomas • M: meningiomas and • E: ependymomas • Rule of 2s • neurofibromatosis type 2 • chromosome 22 (22q12) gene location • bilateral vestibular schwannomas • presents in 2nd-4th decades (around 20 years) • initial prevalence estimated to be 1:200,000
- 36. Megaureter
- 37. Ectopic kidney and pancake kidney
- 38. Horseshoe kidney
- 41. Renal tb
- 44. Bladder tb
- 45. Medullary nephrocalcinosis •HAM HOP Mnemonic •H: hyperparathyroidism •A: (renal tubular) acidosis •M: medullary sponge kidney •H: hypercalcaemia/hypercalciuria •O: oxalosis •P: papillary necrosis
- 47. Cortical nephrocalcinosis •G: (chronic) glomerulonephritis •O: oxalosis •A: Alport syndrome/ Acute cortical necrosis •T: Transplant rejection (Chronic)
- 49. ALD
- 50. Canavans
- 52. Wilson disease
- 53. Leigh syndrome or subacute necrotising encephalomyelopathy (SNEM)
- 55. MS
- 56. TM
- 57. NMO
- 58. ADEM
- 59. SACD
- 63. Spinal AVF
- 64. Diastematomyelia • Diastematomyelia, also known as a split cord malformation, refers to a type of spinal dysraphism (spina bifida occulta) when there is a longitudinal split in the spinal cord.
- 66. Spinal astrocytoma - thoracic
- 68. HOD
- 71. PAGETS
- 72. Signs There are many Paget disease-related signs, listed here and described in the modality- specific sections below: •banana fracture •blade of grass sign •cotton wool appearance of bone •ivory vertebra sign •jigsaw pattern bone or mosaic pattern bone •Lincoln sign •Looser zones •Mickey Mouse sign •osteoporosis circumscripta •picture frame vertebra •Tam o' Shanter sign
- 73. FD
- 75. HPT
- 76. AS
- 77. PSORITIC
- 78. EROSIVE • Erosive osteoarthritis has a predilection for the hands. The dominant features are those of osteoarthritis, particularly in terms of distribution: • distal interphalangeal (DIP) joints • proximal interphalangeal (PIP) joints • first carpometacarpal (CMC) joint • Additional characteristic features include: • diffuse cartilage loss, with joint space narrowing • subchondral erosions (at least two central erosions affecting separate interphalangeal joints); typical central location of the erosions produces the classic "gull-wing" appearance • joint ankylosis • absence of 2 • marginal erosions • fusiform soft-tissue swelling • osteopenia
- 80. RA • MRI is particularly sensitive to the early and subtle features of RA. • Commonly used sequences include T1-weighted contrast-enhanced spin-echo with fat saturation and T2-weighted spin- echo or gradient-echo sequences 2. • Features of RA best demonstrated with MRI include 2: • synovial hyperaemia: an indication of acute inflammation • synovial hyperplasia (rice bodies) • pannus formation • decreased thickness of cartilage • subchondral cysts and erosions: • MRI is much more sensitive than radiography • it is thought that subchondral cysts in RA eventually progress to erosions (i.e. constitute "pre-erosions") • contrast enhancement may distinguish erosions or pre-erosions from degenerative subchondral cysts • juxta-articular bone marrow oedema • joint effusions
- 81. RA
- 82. RA
- 83. GOUT
- 84. Distribution
- 85. NEUROPATHIC • Charcot joint, also known as a neuropathic joint or Charcot (neuro/osteo)arthropathy, refers to a progressive degenerative/destructive joint disorder in patients with abnormal pain sensation and proprioception.
- 87. Chondroblastoma
- 88. Osteochondroma/exostosis • They are usually sporadic, but can be part of: • hereditary multiple exostoses (HME): also known as diaphyseal aclasis • Trevor disease: also known as dysplasia epiphysealis hemimelica
- 89. Chondrosarcoma
- 97. Ewing's
- 98. Osteosarcoma
- 99. Osteosarcoma Calcified mets in lungs
- 100. Parosteal sarcoma
- 102. Synovial sarcomas
- 103. BARIUM
- 106. Barret esophagus
- 107. Apthoid ulcer
- 109. ccam
- 110. Pulmonary Stenosis
- 111. Mitral Stenosis
- 112. CELIAC disease
- 113. Pulmonary sling
- 114. Dermatomyositis
- 115. Gamekeeper thumb
- 116. volvulus
- 119. Zenker’s diverticula
- 122. Meckel's diverticula
- 123. Caustic esophagus
- 124. Neck: Enlarged tonsil and adenoid
- 125. Croup • Croup, also known as acute laryngotracheobronchitis, is due to viral infection of the upper airway by parainfluenza virus or respiratory syncytial virus (RSV)
- 126. Epiglottitis
- 128. Rp abscess
- 129. 2nd brachial cleft cyst
- 130. Many more will be added ……….
- 131. WMD
- 132. SMA , nutcracker, median arcuate syndrome
- 133. RDS
- 134. Meconium aspiration
- 135. TTN
- 136. BPD
- 137. PIE
- 138. CLE
- 139. PUL. Sequestration
- 140. Pedia git/gut(Liver, renal and adrenal) • TEF • Achlasia
- 141. Pedia CVS
Editor's Notes
- Digital subtraction angiogram of the internal carotid artery, lateral view, demonstrates a large tortuous vessel (arrow) passing from the internal carotid artery (open arrow) to the basilar artery (arrowhead), and supplying the posterior circulationLarge persistent trigeminal artery passing from the left ICA to the terminal basilar artery via the cavernous sinus. Note the grossly hypoplastic vertebro-basilar arterial system as a result of this congenital anomaly with most posterior circulation blood coming from the left ICA via the trigeminal artery Persistent primitive trigeminal artery (PPTA) is one of the persistent carotid-vertebrobasilar anastomoses.
- There is direct communication between the basilar artery and left internal carotid artery, in keeping with a persistent left trigeminal artery
- Persistent smooth posterior oesophageal indentation, suggestive of vascular impression
- First vessel from the arch is the left commmon carotid artery. Bilateral calcified pleural plaques. Thrombosed ligamentum arteriosum. Kommerell's diverticulum/dilatation of the origin of the left subclavian artery causes compression of the left brachiocephalic vein resulting in contrast entering the heart via alternative routes
- This anomaly is caused by persistence of the right and left embryonic fourth aortic arches, which results in formation of a vascular ring from the splitting of the ascending aorta into two limbs that pass to either side of the trachea and oesophagus 5 (both of which get encircled), which then join as a single descending aorta
- Aberrant right subclavian arteries (ARSA), also known as arteria lusoria, are one of the commonest of the aortic arch anomalies. Instead of being the first branch (with the right common carotid as the brachiocephalic artery), it arises on its own as the fourth branch, distal to the left subclavian artery. It then hooks back to reach the right side with its relationship to the oesophagus variable: 80% posterior to the oesophagus 15% between oesophagus and trachea 5% anterior to the trachea aneurysmal dilatation (aberrant subclavian arterial aneurysms) of the proximal portion of an aberrant right subclavian artery can occur, a pouch-like aneurysmal dilatation is called a diverticulum of Kommerell
- Aberrant left pulmonary artery, also known as pulmonary sling, represents an anatomical variant characterised by the left pulmonary artery arising from the right pulmonary artery and passing above the right main bronchus and in between the trachea and oesophagus to reach the left lung. It may lead to compression and focal stenosis of the trachea Fluoroscopy In most instances, the barium oesophagogram characteristically shows a mass between the trachea and the oesophagus just above the level of the carina, usually seen as an anterior indentation over the oesophagus
- Post contrast T1 axial imaging demonstrates bilateral enhancing masses in the cerebellopontine angle, larger on the left. Both can be seen extending into the internal acoustic meatii and are consistent with acoustic schwannomas. The fact that they are bilateral almost certainly indicates that the patient has NF2. There are multiple enhancing nodular lesions spread throughout all the spinal canal and going through some vertebral foramina Mixed solid-cystic mass arising from the fourth ventricle and causing mass effect on the brainstem. There was also resultant obstructive hydrocephalus, not shown here. The mass appears to ‘ooze’ out of the foramen of Magendie. There was no associated spinal lesion. Classical ‘plastic’ ependymoma
- Pancake kidney (also known as discoid kidney, disc kidney, lump kidney, fused pelvic kidney or cake kidney) is a rare renal fusion anomaly of the kidneys of the crossed fused variety.
- Characterised by bilateral symmetrical confluent areas of periventricular deep white matter signal change, in particular around the atria and frontal horns with sparing of subcortical U fibres leading to a "butterfly pattern". Progression can lead to cortical and subcortical atrophy T2:affected areas are high signal and may show a "tigroid pattern" on axial plane or "leopard pattern" on sagittal plane representing sparing along the venules subcortical U-fibres are usually spared
- five different MRI patterns of adrenoleukodystrophy based on the involved anatomic locations and MR patterns of progression: deep white matter in the parieto-occipital lobes and splenium of the corpus callosum (66% of cases, chiefly in children); may include lesions of the visual and auditory pathways frontal lobe or genu of the corpus callosum (15.5%, mostly in adolescents) frontopontine or corticospinal projection fibres (12%, mostly in adults) cerebellar white matter (1%, mostly in adolescents) combined parieto-occipital and frontal white matter (2.5%, mostly children) There tends to be cortical and subcortical U-fibre sparing
- MRI confirms the megalencephalic appearance and provides more detail of the white matter disease, which is typically diffuse, bilateral, and involving the subcortical U-fibres
- Diffuse T2 hyperintensities and restricted DWI signal of the pons with extension into the middle cerebellar peduncles. Also similar increased T2 signal of the symmetric basal ganglia, including the caudate nuclei, putamina, as well as the ventrolateral thalami, without the restriction of diffusion. 2. On MRI images seen T2, FLAIR hyperintensity in medulla oblangata, pons, both thalami and putamen, and the caudate nuclei. Additionally an cavum septum pellucidum and cavum vergae.
- There is symmetric marked hyperintense signal intensity on T2/FLAIR imaging and restricted diffusion in the dentate nuclei, inferior cerebellar peduncles, lateral fourth ventricle floor in the expected locations of the vestibular tract and in the expected tract of the vestibular cochlear nerve. Also present, is diffusion restriction in the posterior columns of the proximal cervical cord, anteriorly in the inferior medulla, and punctate symmetric foci of restricted diffusion in the inferior colliculi of the quadrigeminal plate and medial geniculate bodies. There is mild high signal on FLAIR and diffusion weighted imaging involving the bilateral putamen 2nd image is dwi image
- 1. Selected FLAIR MRI images of the brain demonstrates hyperintensities in the periaqueductal region and the medial thalami. Note that this is on a background of global cerebral atrophy with CSF spaces more prominent than would normally be expected for a patient of 45 years old. 2.Hyperintense signals in the bilateral medial thalami and periventricular regions of third ventricle on FLAIR images, consistent with Wernicke encephalopathy 3.Abnormal signal bilateral and symmetrical involving the medial and posterior aspect of both thalami displaying bright signal in DWI, T2 and FLAIR.
- Focal inflammatory disorder of the spinal cord resulting in motor, sensory and autonomic dysfunction. Imaging findings: More than 2/3 of the cross sectional area is involved. Focal enlargement. T2WI hyperintensity Enhancement + / -. Two forms of TM: Acute partial transverse myelitis - APTM Lesions extending less than two Segments. These patients are at risk of developing MS. Acute complete transverse myelitis - ACTM Lesions extending more than two Segments
- Arterial infarction Spinal cord ischemia is typically seen as a complication of aortic aneurysm surgery or stenting. The images are of a patient who developed a paraparesis after stenting of an aortic aneurysm. Notice the high signal ventrally in the chord, which is typical for arterial infarction. On transverse images a typical snake-eye appearance can be seen.
- Notice the high signal in the lower thoracic cord and the surrounding dilated vessels on the T2WI. On the enhanced T1WI there is subtle enhancement.
- T2 hyperintense expansion of the thoracic cord is demonstrated. The main mass effect is centred between T5 and T8 but abnormal high T2 signal extends between T4 and T11. Postcontrast images demonstrate patchy irregular peripheral enhancement of this lesion, and central low intensity. No definite evidence of blood products/haemorrhage although some T2 hypointensity is seen.No further intra medullary lesion is identified.
- Lower thoracic cord is a vividly enhancing nodule with associated prominent serpiginous flow voids both within the mass and over the surface of the cord, and among the cauda equina. It is an isolated abnormality, associated with marked expansion of the entire cord by a large syrinx. Selected MRI images demonstrate multiple enhancing intramedullary lesions, the largest at C4/5, with an associated syrinx.
- 1.Paget involvement of the skull, with widening of the diploic space, typical "cotton wool" appearance and over-riding enlarged frontal bone (Tam o' Shanter sign). 2. Marked thickening of the calvarium. The diploic space is widened and there are ill-defined sclerotic and lucent areas throughout. The cortex is thickened and irregular. 3. Osteosarcoma in Paget disease
- 1.chalk stick fracture-Single sagittal image of the lumbar spine demonstrates a fracture extending from the anterior disc margin, through the inferior body of L1 and through the posterior elements. Note extensive syndesmophytic fusion of the discs spaces and posterior elements consistent with ankylosing spondylitis. 2.Typical features of ankylosing spondylitis with syndesmophytes, bamboo spine and bony fusion of posterior elements (dagger sign). 3.Throughout the spine, the vertebral bodies are fused by marginal syndesmophytes giving the appearance of Bamboo spine.
- 1. Severe joint space narrowing at the first carpometacarpal joint and the interphalangeal joints. At the first carpometacarpal joint there is associated subchondral sclerosis and cyst formation. There are also subchondral central erosions at the heads of the proximal phalanges with marginal osteophytes involving the distal phalangeal bases, demonstrating gull wing deformity through the second and fifth digits. Severe joint space narrowing, subchondral sclerosis, and erosive changes of the scaphoid-trapezium and scaphoid-trapezoid joints. Narrowing of the radiocarpal joint. Diffuse osteopenia. Findings are keeping with erosive osteoarthritic changes 2. Extensive erosive changes and alignment abnormalities are observed along the articular surfaces of the 2nd through 5th PIP and DIP joints bilaterally, as well as at the 1st IP, MCP and carpometacarpal joints bilaterally. These erosive changes assume a gull wing appearance. The alignment abnormalities involving the 1st digits resemble a hitchhiker's thumb. There are no significant erosive changes involving the radiocarpal or intercapral joints, and the 2nd-5th MCP joints are also spared.
- Almost total loss of radiocarpal, carpometacarpal and intercarpal joint spaces associated with multiple radial and carpal bone small subchondral cysts and bony fusion of trapezium, trapezoid and scaphoid bones. Diagnosis: Advanced rheumatoid arthriti
- Erosive changes of intercarpal, carpometacarpal anX-ray (both hands) findings: Loss of intercarpal, carpometacarpal and distal radio-ulnar joint spaces ulnar deviation of MCP joints extension deformity of DIPs (Boutonierre deformity) and hitchhiker thumb deformit d metacarpophalangeal of the 2nd finger of right hand. Left elbow and left knee are affected as well.
- Punched-out juxta-articular erosions of the first and fifth metatarsal heads with overhanging edges are typical for gout. Overlying soft tissue swelling and increased density represent tophi.
- There is destruction and deformity of the tarsal bones characterised by sclerosis, joint space narrowing, cortical irregularities, and loose bodies. Lisfranc injury involving the second to fifth tarsometatarsal joints with lateral dislocation. Cortical thickening and sclerosis involving the proximal second to fifth metatarsal bones. Local soft tissue oedema. Destruction, disorganisation and fragmentation of the subtalar and inter-tarsal joints, associated with soft tissue tumefaction and multiple bone fragments.
- 1. A sharply defined lucent lesion is centred on the epiphysis of the distal femur, and appears to transgress the growth plate (which remains open). It has a narrow zone of transition and no convincing matrix calcification. Anteriorly it appears to abut the articular surface, possibly breaching it. A joint effusion is present. No periosteal reaction is present 2.Chondroblastoma in right lateral femoral condyle with low T1W and high T2W/STIR internal signal and surrounding bone marrow oedema
- 2. A large posteromedial bony projection is demonstrated involving the distal one quarter of the femoral shaft. It is continuous with the medullary cavity and has an irregular medial margin without large soft tissue component or fracture. Severe narrowing of the medial and patellofemoral joint compartments and marginal osteophyte formations indicate degenerative disease of the knee.
- There are numerous similar-sized intra-articular loose bodies of variable signal intensity, some of them are showing intermediate to high signal intensity that is of cartilage. Others have low signal intensity at the periphery, which represents ossification. The joint capsule is distended with a little fluid and these numerous loose bodies Synovial chondromatosis (osteochondromatosis or synovial chondrometaplasia) also known as Reichel syndrome, is a disorder characterised by loose cartilaginous bodies which may, or may not be calcified or ossified. It is classified under two main types: primary synovial chondromatosis: predominantly monoarticular disorder of unknown aetiology secondary synovial chondromatosis: resulting in intra-articular loose bodies from causes such as trauma, osteoarthrosis and neuropathic arthropathy
- "Cloud-like" calcifications in the region of the triceps insertion, olecranon, and olecranon bursa (3.3 x 7.7 x 5.7 cm). There is no connection to the underlying humerus or ulna. Bilateral extensive soft tissue calcification posterior to the elbow joint around the insertion of triceps. US confirmed that it was extra-articular. Limitation of extension at the elbow.
- Hypertrophic phenomena and gross heterogeneous muscle calcifications that extend from the pelvis to the middle third of the thighs. A firearm projectile is located in the soft tissues in left inguinal region. Notice that the bone cortical isn't affected Myositis ossificans is a benign process characterised by heterotopic ossification usually within large muscles. The diagnosis is usually based on the patient's history (of trauma),
- he distal half of the femur is occupied and expanded with a heterogeneous mass with areas of bone formation. Posterior the periosteum is elevated (Codman's triangle).
- There is a lobulated juxtacortical mass with dense calcification and smooth borders arising from the lateral cortex of the right femoral metaphysis measuring approximately 5.8 x 3.3 x 9.3 cm. There is no aggressive periosteal reaction. Superiorly, a thin radiolucent line separates the tumour from the cortex. Ill-defined calcified/ossified mass arising from the lateral aspect of distal femu
- Synovial sarcomas are relatively common intermediate-to-high grade malignant soft tissue tumours, often with an initial indolent course, affecting young patients, and most commonly involving the soft tissue surrounding the knees
- Lobulated mass-like density in the left lung adjacent to the heart border. A prominent vessel is noted extending to the mass from the pulmonary hilum. Appearance is suggestive of a pulmonary arteriovenous malformation. After adjusting the image contrast, a similar lesion is seen in the right lung base behind the diaphragm.
- Large wide necked diverticulum arising several centrimetres proximal to the GOJ. The diverticulum contains a progressively filling air fluid-level following barium consumption. Normal calibre oesophagus - no stricture. No hiatus hernia.
- Characteristic tapering of the upper trachea (steeple sign) on an AP radiograph which was suspicious for croup in this clinical context. Lateral x-ray of the neck demonstrates distension of hypopharynx and subglottic oedema consistent with croup.
- Epiglottitis. Lateral radiograph of the neck demonstrates and enlarged epiglottis (red arrow) and thickening of the aryepiglottic folds (yellow arrow). There is also reversal of the normal lordotic curve in the cervical spine and slight dilatation of the hypopharynx
- Annotations showing the normal width of the pre-vertebral soft tissue at the various cervical levels. The annotated pathological images reveals the magnitude of the soft tissue widening.
- Huge fluid-gas filled rim enhancing abscess in the retropharyngeal space. Its extends over nearly the whole length of the cervical spine.