spotters
Torch infection
• Intracranial Calcifications
• CMV: Periventricular calcifications
• Toxoplasmosis: Diffuse, scattered intracranial
calcifications
• Hydrocephalus & Ventriculomegaly
• Seen in Toxoplasmosis and CMV
• Hirayama disease
• Rare, non-progressive lower motor neuron
disorder
• Neutral and flexion MRI showing anterior
translation of posterior dura on flexion MR
with flow voids and associated cord thinning
Cervical myelomeningiocele
• Absent posterior neural elements of cervical
vertebrae with herniation of the cord through
this defect to project into large
myelomeningocele
Vestibular Schwannoma
• “Ice Cream Cone” Appearance on MRI:
• Scoop = mass in the cerebellopontine angle (CPA)
• Cone = extension into the internal auditory canal (IAC)
• Clinical Findings:
• Unilateral sensorineural hearing loss (most common)
• Tinnitus
• Imbalance or vertigo
• Possible facial numbness or weakness (if large tumor
compresses CN V or VII)
Pericallosal lipoma
• T1 hyperintense fat intensity lipoma noted in
the peri callosal region
• Associations:
• Corpus callosum agenesis or dysgenesis
• Other midline anomalies (e.g., interhemispheric
cysts)
Erdheim-Chester Disease (ECD)
• Rare non-Langerhans cell histiocytosis
characterized by xanthogranulomatous infiltration of
multiple organs, especially bones, kidneys, and CNS.
• Classic Imaging Sign: Hairy Kidney Sign –
symmetric perirenal soft tissue infiltration on CT/MRI
due to retroperitoneal involvement
Jeune Syndrome (Asphyxiating Thoracic
Dystrophy)
• Radiological Hallmark: Bell-shaped narrow thorax
with short, horizontally oriented ribs—leads to
respiratory distress in infancy.
• Skeletal Dysplasia: Rare autosomal recessive
condition with shortened long bones, polydactyly,
and renal/liver involvement in some case
Agenesis of carpous callosum
• Congenital absence (partial or complete) of the
corpus callosum causing variable
neurodevelopmental symptoms like seizures and
developmental delay.
• Radiology: Neurosonogram shows widely spaced,
parallel lateral ventricles with absent cavum septum
pellucidum and elevated frontal horns (“racing car”
sign)
Ewings sarcoma
• Malignant bone tumor commonly affecting
diaphysis of long bones in children and adolescents.
• Classic radiological sign: "Onion-skin" periosteal
reaction on X-ray due to layered new bone
formation.
Ebstein anomaly
• Congenital malformation with apical displacement
of the tricuspid valve leaflets causing “atrialization”
of the right ventricle.
• Chest X-ray shows a “box-shaped” enlarged heart
with cardiomegaly and a prominent right atrium.

Radiology spotters powerpoint presentation

  • 1.
  • 3.
    Torch infection • IntracranialCalcifications • CMV: Periventricular calcifications • Toxoplasmosis: Diffuse, scattered intracranial calcifications • Hydrocephalus & Ventriculomegaly • Seen in Toxoplasmosis and CMV
  • 5.
    • Hirayama disease •Rare, non-progressive lower motor neuron disorder • Neutral and flexion MRI showing anterior translation of posterior dura on flexion MR with flow voids and associated cord thinning
  • 7.
    Cervical myelomeningiocele • Absentposterior neural elements of cervical vertebrae with herniation of the cord through this defect to project into large myelomeningocele
  • 9.
    Vestibular Schwannoma • “IceCream Cone” Appearance on MRI: • Scoop = mass in the cerebellopontine angle (CPA) • Cone = extension into the internal auditory canal (IAC) • Clinical Findings: • Unilateral sensorineural hearing loss (most common) • Tinnitus • Imbalance or vertigo • Possible facial numbness or weakness (if large tumor compresses CN V or VII)
  • 11.
    Pericallosal lipoma • T1hyperintense fat intensity lipoma noted in the peri callosal region • Associations: • Corpus callosum agenesis or dysgenesis • Other midline anomalies (e.g., interhemispheric cysts)
  • 13.
    Erdheim-Chester Disease (ECD) •Rare non-Langerhans cell histiocytosis characterized by xanthogranulomatous infiltration of multiple organs, especially bones, kidneys, and CNS. • Classic Imaging Sign: Hairy Kidney Sign – symmetric perirenal soft tissue infiltration on CT/MRI due to retroperitoneal involvement
  • 15.
    Jeune Syndrome (AsphyxiatingThoracic Dystrophy) • Radiological Hallmark: Bell-shaped narrow thorax with short, horizontally oriented ribs—leads to respiratory distress in infancy. • Skeletal Dysplasia: Rare autosomal recessive condition with shortened long bones, polydactyly, and renal/liver involvement in some case
  • 17.
    Agenesis of carpouscallosum • Congenital absence (partial or complete) of the corpus callosum causing variable neurodevelopmental symptoms like seizures and developmental delay. • Radiology: Neurosonogram shows widely spaced, parallel lateral ventricles with absent cavum septum pellucidum and elevated frontal horns (“racing car” sign)
  • 19.
    Ewings sarcoma • Malignantbone tumor commonly affecting diaphysis of long bones in children and adolescents. • Classic radiological sign: "Onion-skin" periosteal reaction on X-ray due to layered new bone formation.
  • 21.
    Ebstein anomaly • Congenitalmalformation with apical displacement of the tricuspid valve leaflets causing “atrialization” of the right ventricle. • Chest X-ray shows a “box-shaped” enlarged heart with cardiomegaly and a prominent right atrium.

Editor's Notes

  • #4 Young man with hand wasting that worsen on neck flexion
  • #6 Congenital midline neck swelling with neurologic defecit
  • #8 Middle age adult with unilateral hearing loss and imbalance
  • #10 Fat density midline mass near corpus callosum in child with seizure or incidental finding
  • #12 Middle aged adult with bilateral symmetric long bone sclerosis and systemic involvement