Articles

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More than 200 results
Article

Spleen size (pediatric)

The spleen size varies with a child's age. The three numbers below represent the 10th percentile, median, and 90th percentile for the long axis of the spleen (cm) 1-3: 0-3 months: (3.3, 4.5, 5.8 cm) 3-6 months: (4.9, 5.3, 6.4 cm) 6-12 months: (5.2, 6.2, 6.8 cm) 1-2 years: (5.4, 6.9, 7.5 cm)...
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Leukodystrophies

Leukodystrophies are a heterogeneous group of disorders that primarily affect the white matter of the central nervous system. They are particularly encountered in childhood as many are genetically determined and represent abnormalities in white matter metabolism. A number of leukodystrophies can...
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Parkes Weber syndrome

Parkes Weber syndrome or less commonly F P Weber syndrome is a traditional eponymous denomination of a certain type of angiodysplasia, that would nowadays rather be called a mixed hemolymphatic congenital vascular malformation (CVM) with arteriovenous (AV) shunting, based on the Hamburg classifi...
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Dacryocystocele

Dacryocystoceles are caused by obstruction of both the proximal and distal ends of the nasolacrimal duct. An imperforate Hasner valve causes the distal blockage, but the cause of proximal obstruction is less clearly understood but the Rosenmuller valve has been implicated.  Epidemiology Dacryo...
Article

Herpes simplex encephalitis

Herpes simplex (HSV) encephalitis is the most common cause of fatal sporadic fulminant necrotizing viral encephalitis and has characteristic imaging findings.  Two subtypes are recognized which differ in demographics, virus, and pattern of involvement. They are 1: neonatal herpes encephalitis ...
Article

J-shaped sella

A J-shaped sella is a variant morphology of the sella turcica, whereby the tuberculum sellae is flattened, thus forming the straight edge of the "J". The dorsum sellae remains rounded and forms the loop of the "J". Differential diagnosis Differential diagnosis for a J-shaped sella includes 1,2...
Article

Astroblastoma, MN1-altered

Astroblastomas are rare glial tumors usually found in the cerebral hemispheres of young adults and children.  Terminology The exact nature of astroblastomas remains to be fully elucidated. Tumors with compatible histological features have a variety of molecular characteristics and overlap with...
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Congenital talipes equinovarus

Congenital talipes equinovarus is considered the most common anomaly affecting the feet diagnosed on antenatal ultrasound. Terminology While some use talipes equinovarus and clubfoot synonymously, in certain publications, the term clubfoot is considered a more general descriptive term that des...
Article

Complications of radiation therapy

Radiation therapy has the potential to cause complications in many organ systems, many of which, especially in the thorax, are important for radiologists to be aware of.  acute radiation syndrome complications of cranial radiation therapy radiation-induced cerebral vasculopathy radiation-ind...
Article

Hemolytic uremic syndrome

Hemolytic uremic syndrome (HUS) is a multisystem thrombotic microangiopathic disease characterized by the triad of renal failure, hemolytic anemia and thrombocytopenia. It is the most common cause of renal failure in infancy and childhood requiring dialysis.  There are two forms of this syndrom...
Article

Chiari I malformation

Chiari I (Chiari 1) malformation is the most common variant of the Chiari malformations and is characterized by a caudal descent of the cerebellar tonsils through the foramen magnum. Symptoms are generally proportional to the degree of descent. MRI is the imaging modality of choice. Treatment wi...
Article

Salter-Harris type I fracture

Salter-Harris type I fractures are relatively uncommon injuries that occur in children. Salter-Harris fractures are injuries where a fracture of the metaphysis or epiphysis extends through the physis. Not all fractures that extend to the growth plate are Salter-Harris fractures. Radiographic fe...
Article

Upper limb radiography (pediatric)

Upper limb radiography involves plain film imaging of the shoulder, humerus, ulna, radius, metacarpals and carpal bones in pediatric patients. Depending on the patients' age, the difficulty of the examination will vary, often requiring a specialist trained radiographer familiar with a variety of...
Article

Sinding-Larsen-Johansson disease

Sinding-Larsen-Johansson disease, also known as Sinding-Larsen disease or Larsen-Johansson syndrome, affects the proximal end of the patellar tendon as it inserts into the inferior pole of the patella. It represents a chronic traction injury of the immature osteotendinous junction. It is a close...
Article

SAPHO syndrome

The SAPHO syndrome is an acronym that refers to a rare syndrome that is manifested by a combined occurrence of 2: S: synovitis A: acne P: pustulosis H: hyperostosis O: osteitis Epidemiology SAPHO classically tends to present in young to middle-aged adults. Presentation in the pediatric po...
Article

Isolated greater trochanteric fracture

Isolated greater trochanteric fractures most commonly result from forceful muscle contraction of a fixed limb, which usually occurs in those who are young and physically active. Epidemiology Isolated trochanteric fractures are more common in young, active males, usually between the ages of 14 ...
Article

Abdomen radiograph (pediatric)

The abdomen radiograph is a commonly requested examination in the pediatric patient. Children that present for abdominal x-rays are often very unwell, therefore specialized techniques and appropriate communication are essential for gaining the child's cooperation.  Indications Performing abdom...
Article

Forearm fracture

Forearm fractures are a group of fractures that occur in the forearm following trauma. The radius and ulna are bound together at the proximal and distal radioulnar joints and act as a ring. Like elsewhere in the body, it is difficult to only fracture one bone if there is a bony ring. If the radi...
Article

Epilepsy

Epilepsy is a common neurological disorder that is characterized by a predisposition to having epileptic seizures and can take many clinical forms and have many potential etiologies. Epilepsy is defined by the International League Against Epilepsy (ILAE) as 1: at least two or more unprovoked (...
Article

Köhler disease

Köhler disease is an eponymous term referring to childhood-onset osteonecrosis of the navicular in the foot. Müller-Weiss syndrome is the adult counterpart of navicular osteonecrosis 4,5. Epidemiology Köhler disease typically presents in the pediatric population (4-6 years of age) and there is...

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