6. • Clay shoveler’s fracture -spinous process of C7
• Jefferson fracture- Atlas C1
• Hangman fracture- Axis C2
7.
8. UTERINE DIDELPHYS
• Type of Mullerian duct anomaly.
• Complete duplication of uterine horns and cervix with no
communication b/w them.
9.
10. INTRAOSSEOUS LIPOMA
• Nonaggressive radiolucent lesion with sharply defined
borders, associated with thinning and bulging of the cortex.
• The central calcifications and ossifications are frequently
present.
• Common sites – fibula, calcaneum and rib.
12. TOXOPLASMOSIS
• Multiple lesions
• Predilection for basal ganglia, thalami and corticomedullary
junction.
• Post contrast MR – Ring enhancement, typically thin and
smooth.
14. INSULINOMA
• Small (90 % are < 2 cm) and hyper vascular.
• May contain calcification.
• 10 % malignant.
• Whipple’s triad
Fasting hypoglycaemia
Symptoms of hypoglycaemia
Immediate relief of symptoms after IV glucose.
15.
16. CHONDROSARCOMA
• Large masses; 4 to 10cm or more in size at the time of
diagnosis.
• Show characteristic ring and arc/ popcorn type of matrix
mineralization.
17.
18. SIRENOMELIA OR
MERMAID SYNDROME
• Fusion of lower limb structures with varying degrees of sacral
agenesis
• Maybe associated with oligohydramnios antenatally
• Vascular steal phenomenon causing ischemia to caudal
portion of fetus.
19.
20. SCHIZENCEPHALY
• Grey matter lined cleft extending from the ependyma to the pia
mater.
Two types
• open lip
– the cleft walls are separated and filled with CSF
– most common form in bilateral cases.
• closed lip
– the cleft walls are in apposition
– most common form in unilateral cases
21.
22. FORM A for registration or renewal of registration of
genetic counselling center/ genetic laboratory, genetic
clinic/ ultrasound clinic/ imaging center
23.
24. • Unicameral bone cyst.
• 3- to 14-year age range.
• Proximal humerus : most common 50-60%, proximal femur : 30% ,other long bones,
calcaneum, talus.
RADIOLOGIC FEATURES
• Well defined geographic lucent lesions with a narrow zone of transition, mostly seen in
skeletally immature patients, which are centrally located and show a sclerotic margin in
the majority of cases with no periosteal reaction or soft tissue component.
SIMPLE BONE CYST
28. LYMPHANGIOMYOMATOSIS
• multi-system disorder that can occur either
sporadically or in association with
the tuberous sclerosis complex (TSC)
• exclusively affects women of childbearing age
• present with exertional dyspnoea and
recurrent episodes of pneumothorax
29. Radiograph
• Chylothorax : chylous pleural effusion
• evidence of hyperinflation
• diffuse bilateral reticulonodular densities
HRCT
• thin walled cysts of variable sizes surrounded by normal
lung parenchyma can be seen throughout the lung
• interlobular septal thickening
• may show a dilated thoracic duct
• haemorrhages may be seen as areas of increased
attenuation
30.
31. LANGERHANS CELL HISTIOCYTOSIS aka
EOSINOPHILIC GRANULOMA
• Solitary or multiple punched out lytic lesions without sclerotic
rim
• Geographic skull
38. INTRAVERTEBRAL VACCUM CLEFT SIGN
• Transverse, linear, or semilunar radiolucency located
within the vertebral body.
• Represents gas (principally nitrogen) in the fracture line
of the vertebral body.
• Pathogenesis of this process is not completely clear.
• Mostly suggestive of ischemic necrosis of bone.
• Reported in association with Kümmell disease, a delayed
posttraumatic collapse of the vertebral body.
42. Holoprosencephaly
• Congenital brain malformation resulting from incomplete
separation of the two hemispheres.
• Alobar – most severe
• Semi lobar
• lobar
43. Alobar holoprosencephaly
• single midline monoventricle (or holosphere)
– lateral and third ventricles are absent
• absent midline structures
– absent septum pellucidum
– agenesis or hypoplasia of the corpus callosum
– absent interhemispheric fissure and falx cerebri
– absent olfactory tract