Articles

Articles are a collaborative effort to provide a single canonical page on all topics relevant to the practice of radiology. As such, articles are written and edited by countless contributing members over a period of time. A global group of dedicated editors oversee accuracy, consulting with expert advisers, and constantly reviewing additions.

102 results found
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≤11 ribs (differential)

≤11 ribs is associated with a number of congenital abnormalities and skeletal dysplasias, including: Down syndrome (trisomy 21) campomelic dysplasia kyphomelic dysplasias asphyxiating thoracic dysplasia (Jeune syndrome) short rib polydactyly syndromes trisomy 18 chromosome 1q21.1 deletion...
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Absent septum pellucidum

An absent septum pellucidum may rarely be an isolated finding, or more commonly be seen in association with a variety of conditions. Epidemiology The septum pellucidum is partly or entirely absent in 2 or 3 individuals per 100,000 in the general population.  Pathology An absent septum pelluc...
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Acute abdominal pain

Acute abdominal pain is a common acute presentation in clinical practice. It encompasses a very broad range of possible etiologies and diagnoses, and imaging is routinely employed as the primary investigative tool in its modern management. Terminology A subgroup of patients with acute abdomina...
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Airway foreign bodies in children

Airway foreign bodies in children are potentially fatal, which is why immediate recognition is important. Unfortunately, delayed diagnosis is common. Epidemiology Children under the age of four years are at increased risk of foreign body (FB) aspiration, with a slight male predominance 1.  Cl...
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Alpha fetoprotein

Alpha fetoprotein (AFP) is an important plasma protein synthesized by the yolk sac and fetal liver. In adults its main utility is as a tumor marker, primarily for hepatocellular carcinoma or teratoma. Functionally it is the fetal homologue of albumin, i.e. it acts as a major carrier protein in t...
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Alternating radiolucent and radiodense metaphyseal lines

Alternating radiolucent and radiodense metaphyseal lines can be seen with a number of conditions and the differential diagnosis is wide: growth arrest lines bisphosphonate therapy rickets: especially those on prolonged treatment, e.g. vitamin D dependent rickets osteopetrosis chemotherapy ...
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Anoxic brain injury

Anoxic brain injury, also known as global hypoxic-ischemic injury, is seen in all age groups (from antenatal to the elderly) as a result of numerous etiologies. The pattern of injury depends on a number of factors including: age of the patient (brain maturity) neonatal hypoxic-ischemic encepha...
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Anterior vertebral body beaking

Anterior vertebral body beaking occurs in a number of conditions and may emanate from the central portion or the lower third of the vertebral body. Middle third Morquio syndrome 1 (middle for Morquio) Lower third Hurler syndrome 2 achondroplasia 3 pseudoachondroplasia 4 cretinism 5 Down ...
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Asplenia syndrome

Asplenia syndrome (also known as right isomerism or Ivemark syndrome) is a type of heterotaxy syndrome. Epidemiology There is an increased male predilection. Asplenia syndrome is usually diagnosed in neonates 4. Clinical manifestation In contrast to polysplenia syndrome, most patients die be...
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Benign liver tumors (pediatric)

Pediatric benign liver tumors are a relatively rare, but important group of conditions. Importantly, the commonest cause of a benign liver tumor is specific to the pediatric population. The list in descending order of frequency is: infantile hepatic hemangioma (previously hemangioendothelioma) ...
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Bent bone dysplasias (differential)

Bent bone dysplasias are a class of dysplasia included in a 2010 classification of genetic skeletal disorders 1. campomelic dysplasia Stuve-Weidemann dysplasia kyphomelic dysplasias, a diverse class, including congenital bowing of the long bones cartilage-hair hypoplasia (CHH; metaphyseal d...
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Birth trauma

Birth trauma relates to those conditions caused by both physical/mechanical and hypoxic injuries. Epidemiology Birth trauma occurs in ~5 per 1000 births 2. Risk factors asphyxia breech presentation shoulder dystocia instrument delivery macrosomia obstructed labor Pathology Etiology T...
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Blalock-Taussig shunt

Blalock-Taussig shunt, also known as Blalock-Thomas-Taussig shunt, is a palliative procedure designed to increase pulmonary arterial blood flow in patients with right ventricular outflow tract obstruction (e.g. tetralogy of Fallot) or during initial staged repair of hypoplastic left heart syndro...
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Bone within a bone appearance

Bone within a bone is a descriptive term applied to bones that appear to have another bone within them. There are numerous causes including: normal thoracic and lumbar vertebrae (neonates and infants) growth recovery lines (after infancy) cortical splitting and new periostitis sickle cell d...
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Bronchial atresia

Bronchial atresia is a developmental anomaly characterized by focal obliteration of the proximal segment of a bronchus associated with hyperinflation of the distal lung.  On imaging, it commonly presents as a proximal focal tubular shaped opacity radiating from the hilum associated with a dista...
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Cardiovascular shunts

Cardiovascular (cardiac) shunts are abnormal connections between the pulmonary and systemic circulations. Most commonly they are the result of congenital heart disease. Pathology Blood can either be shunted from the systemic circulation to pulmonary circulation (i.e. 'left-to-right shunt') or ...
Article

Childhood malignancies

Unfortunately the pediatric population is susceptible to malignancies. The most common entities, in overall order of frequency, are 1-4: leukemia/lymphoma: ~35% * acute lymphoblastic leukemia: 23% Hodgkin disease: 5% acute myelogenous leukemia: 4% central nervous system malignancies: ~20% ...
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Chronic suppurative lung disease

Chronic suppurative lung disease (CSLD) refers to a group of conditions which includes: cystic fibrosis  bronchiectasis primary ciliary dyskinesia This term is usually used in the context of pediatric patients.
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COL4A1-related disorders

COL4A1-related disorders are a group of autosomal dominant disorders caused by a mutation in the COL4A1 gene. Epidemiology The exact prevalence is unknown, but the group of disorders is considered to be under-recognized, especially asymptomatic variants 1. Clinical presentation The clinical ...
Article

Colpocephaly

Colpocephaly is a descriptive term for a disproportionate prominence of the occipital horns of the lateral ventricles. It can result from a wide range of congenital insults. Clinical presentation Patients may present with motor abnormalities, cognitive deficit, visual abnormalities, and seizur...
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Congenital limb amputation

Congenital limb amputation is the absence of a fetal limb or part of a limb that usually occurs due to disruption of vascular supply. Epidemiology Congenital amputations occur in 0.5 (range 0.03-1) per 1000 live births 2.  Pathology They are slightly more common in the upper limb (60%) than ...
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Congenital renal anomalies

Congenital renal anomalies comprise of vast spectrum of pathologies and include: renal agenesis renal dysgenesis congenital renal hypoplasia congenital megacalyectasis congenital cystic renal disease infantile polycystic renal disease: autosomal recessive polycystic kidney disease (ARPKD):...
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Coronal vertebral cleft

Coronal vertebral clefts refer to the presence of radiolucent vertical defects on a lateral radiograph.   Epidemiology It is most often seen in premature male infants 1,3. As they can occur as part of normal variation (especially in the lower thoracic-upper lumbar spine of premature infants) t...
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Cyanotic congenital heart disease

A number of entities can present as cyanotic congenital heart disease. These can be divided into those with increased or decreased pulmonary vascularity (pulmonary plethora): increased pulmonary vascularity total anomalous pulmonary venous return (TAPVR) (types I and II) transposition of the ...
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Cystic lung lesions (pediatric)

Cystic lesions in pediatric patients are usually congenital lesions and, as such, can be seen antenatally and following delivery. Pathology Etiology Congenital These congenital lesions are predominantly covered by the overarching diagnosis of bronchopulmonary foregut malformation. This is a ...
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Cystic mass adjacent to the angle of mandible (differential)

The differential diagnosis of a cystic mass adjacent to the angle of mandible includes: 2nd branchial cleft cyst lymphatic malformation (lymphangioma) cystic lymphadenopathy from tuberculosis from metastatic squamous cell carcinoma  from metastatic papillary thyroid cancer See also cys...
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Delayed bone age

A generalized retardation in skeletal maturation has different causative or etiological factors, these can be classified as follows: chronic ill health congenital heart disease (especially cyanotic) chronic renal disease inflammatory bowel disease malnutrition: failure to thrive (FTT) rick...
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Dense metaphyseal bands (differential)

The differential diagnosis of dense metaphyseal bands is wide. Differential diagnosis Common chronic anemia, e.g. sickle cell disease, thalassemia chemotherapy, e.g. methotrexate growth acceleration lines following growth arrest due to systemic illness or stress in infancy or childhood, e.g...
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Double bubble sign (duodenum)

The double bubble sign is seen in infants and represents dilatation of the proximal duodenum and stomach. It is seen in both radiographs and ultrasound, and can be identified antenatally 2. Pathology Causes include 1,2: congenital obstruction duodenal web duodenal atresia duodenal stenosis...
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Epicondyle fracture

Epicondyle fractures are common injuries in children. They represent 10% of all elbow fractures in children and usually occur in boys after a fall on an outstretched arm. Medial epicondyle fractures comprise most of these injuries. They can usually be treated with splinting and early physiother...
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Ewing sarcoma family of tumors

Ewing sarcoma family of tumors are a group of small round blue cell tumors that are closely histogenetically related, all demonstrating non-random t(11;22)(q24;q12) chromosome rearrangement resulting in the formation of the EWS-ETS fusion gene 1-3.  Terminology Although the literature is litte...
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Fetal tumors

Although rare, a number to tumors may be diagnosed antenatally. These fetal tumors are a diverse and a unique group of conditions, and include: neuroblastoma: most common tumor overall teratomas sacrococcygeal teratoma head and neck teratoma/epignathus mediastinal teratoma intrapericardial...
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Fibrous hamartoma of infancy

Fibrous hamartoma of infancy is a rare benign tumor of the subcutaneous tissues seen in children. More than 90% of cases present in the first year of life with up to 25% being congenital 1. Epidemiology There is a reported male:female ratio of 2:1 but the exact incidence is unknown 2. Clinica...
Article

Frontal bossing

Frontal bossing is a calvarial radiographic feature where the front of the skull appears protruding anteriorly. It is best appreciated on a sagittal or lateral image. Pathology This feature can be seen in many conditions (in alphabetical order): 18q syndrome acromegaly achondroplasia ß-tha...
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Gallbladder ghost triad

Gallbladder ghost triad is a term used on ultrasound studies when there is a combination of three gallbladder features on biliary atresia: atretic gallbladder, length less than 19 mm irregular or lobular contour  lack of smooth/complete echogenic mucosal lining with an indistinct wall
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Generalized increased bone density in children

The causes of generalized increased bone density in pediatric patients can be divided according to a broad category of causes: skeletal dysplasias osteopetrosis pyknodysostosis metabolic renal osteodystrophy poisoning lead dense metaphyseal bands cortex and flat bones may also be slight...
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Glycogen storage disease

Glycogen storage disease (GSD) refers to a number of syndromes which are characterized by a defect in synthesis, metabolism or storage of glycogen. Pathology There are many types of GSD: type I: von Gierke disease type II: Pompe disease type III: Cori or Forbes disease type IV: Andersen di...
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Gonadal dysgenesis

Gonadal dysgenesis refers to a spectrum of anomalies with abnormal development of the gonads. It falls under the even broader group of disorders of gender development. Pathology In many cases the gonads are replaced by fibrous tissue. Subtypes complete gonadal dysgenesis (CGD) / Swyer syndro...
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Hepatosplenomegaly

Hepatosplenomegaly is simply the simultaneous presence of a pathologically-enlarged liver (hepatomegaly) and spleen (splenomegaly). Pathology Etiology Infection Many, many infections can produce a mild concurrent enlargement of the liver and spleen. This list is by no means exhaustive! vira...
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Hiccups

Hiccups (or hiccoughs), medical term singultus (rarely used), are an unpleasant phenomenon, experienced by everyone on occasion, and usually self-limiting. However the much rarer intractable chronic form can be extremely debilitating. Epidemiology Hiccups are a symptom that has probably been e...
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Increased bone age

A generalized acceleration in bone maturation can result from a number of etiological factors. They include: endocrine disorders idiopathic isosexual precocious puberty hypothalamic or parathalamic lesion with sexual precocity: e.g. craniopharyngioma astrocytoma hypothalamic hamartoma hyp...
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Ingested foreign bodies in children

Ingested foreign bodies in children are common as the world is a curious place to young children, who will put anything and everything into their mouth, and will often inadvertently swallow.  The usual practice is for plain films of the chest/abdomen to identify a foreign body. Epidemiology T...
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Innominate artery compression syndrome

Innominate artery compression syndrome, also known as brachiocephalic artery compression syndrome, is a rare cause of tracheal stenosis that occurs in the pediatric population. Radiographic features The brachiocephalic or innominate artery usually takes its origin to the left of the trachea. T...
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Intestinal failure

Intestinal failure is when a patient's native bowel is unable to digest and absorb the food, electrolytes, and fluids needed for normal growth and development.  Clinical presentation This often includes intractable diarrhea, weight loss, dehydration, electrolyte imbalance, and malnutrition. P...
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Intestinal nonrotation

Intestinal nonrotation is a congenital anomaly of the intestines that results in the small bowel occupying the right side of the peritoneal cavity and the colon predominantly on the left. It is sometimes thought of as a subtype of intestinal malrotation. Epidemiology Nonrotation is estimated ...
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Intestinal transplant

Intestinal transplantation is a surgical treatment for intestinal failure. It is one of the most rarely performed transplant procedures performed, exclusively involving the transplantation of donor small bowel to a recipient, with an ileostomy formation.  Due to the high risk of complications w...
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Intra-abdominal calcification (neonatal)

Intra-abdominal calcification in a neonate can be caused by a number of pathologies that cause calcification within the peritoneal space or within organs. Pathology Etiology Meconium peritonitis The commonest cause is meconium peritonitis which is the result of aseptic peritonitis secondary ...
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Intracranial cystic lesions in the perinatal period

Intracranial cystic lesions in the perinatal period can carry a relatively wide differential which includes: Supratentorial cystic lesions cysts arachnoid cyst choroid plexus cyst connatal cyst holoprosencephaly multicystic encephalomalacia periventricular leukomalacia porencephalic cys...
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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...
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Juvenile osteoporosis

Juvenile osteoporosis refers to osteoporosis occurring in children. Pathology Etiology It can arise from a number of causes 1-4: primary conditions osteogenesis imperfecta Bruck syndrome osteoporosis pseudoglioma syndrome Ehlers-Danlos syndrome Marfan syndrome homocystinuria secondary...
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Lateral epicondyle fracture

Lateral epicondyle fractures are rare epicondylar fractures. They are much rarer than medial epicondyle fractures and represent avulsion of the lateral epicondyle. They are usually seen in the setting of other injuries 1-3.  Epidemiology Incidence typically peaks in the pediatric age group (6-...
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Lead poisoning

Lead poisoning or plumbism is a multisystem condition due to the way in which lead interferes with the function of virtually every organ system. Plumbism most severely manifests due to its devastating effects on the CNS, but it also has important deleterious consequences on the skeletal, renal, ...
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Leg bowing in children

Leg bowing in children is common and often developmental. Differential diagnosis The differential includes: developmental bowing exaggeration of normal age-related angulation changes at the knee neonates and infants normally have varus angulation that gradually corrects within 6 months of w...
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Leukodystrophies

The 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...
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Liver lesions (pediatric)

Pediatric liver lesions are a heterogeneous group that include infiltrative lesions and those that demonstrate mass effect. Moreover, they may be solitary or multiple, benign or malignant: benign liver tumors malignant liver tumors Epidemiology There are differing frequencies of both benign ...
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Lytic skull lesion

Lytic skull lesions have a relatively wide differential that can be narrowed, by considering if there are more than one lesion and whether the mandible is involved. Pathology Causes lytic skeletal metastases multiple myeloma epidermoid - scalloped border with a sclerotic rim eosinophilic g...
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Malignant liver tumors (pediatric)

Pediatric malignant liver tumors are rare, some of which occur only in children but that are similar to those that occur in adults. Epidemiology Malignant liver tumors account for ~1% of pediatric malignancies 2. Pathology Broadly, any malignant liver mass can be defined as a metastasis or p...
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Medial epicondyle fracture

Medial epicondyle fractures represent almost all epicondyle fractures and occur when there is avulsion of the medial epicondyle. They are typically seen in children, and can be challenging to identify. Failure to diagnose these injuries can lead to significant long term disability.  Epidemiolog...
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Meningocele

Meningoceles are protrusions of the meninges through a defect or weak point in the skull or spine, usually involving the soft tissues beneath the surface of the skin. They are typically categorized into congenital, iatrogenic (e.g. following a craniotomy, sinus surgery, or as a laminectomy compl...
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Metaphyseal blanch sign

The metaphyseal blanch sign (a.k.a. metaphyseal blanch sign of Steel) is one of the signs seen on AP views of the adolescent hip indicating posterior displacement of the capital epiphysis. It is a crescent-shaped area of increased density, that overlies the metaphysis adjacent to the physis on ...
Article

Mucopolysaccharidoses

Mucopolysaccharidoses (MPS) constitute a group of hereditary disorders, one of a number of lysosomal storage disorders, having in common an excessive accumulation of mucopolysaccharides secondary to deficiencies in specific enzymes (lysosomal hydrolases) responsible for degradation of mucopolysa...
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Neonatal encephalopathy

Neonatal encephalopathy is a clinical syndrome referring to signs and symptoms of abnormal neurological function in the first few days of life in a neonate born at or beyond 35 weeks of gestation. It is described as difficulty with initiating and maintaining respiration, depression of tone and r...
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Neonatal lines and tubes

Neonatal lines and tubes are widely used in the NICU (neonatal intensive care unit) in the management of critically ill neonates. Examples include: nasogastric (NG) tube endotracheal (ET) tube central venous line umbilical artery catheter umbilical vein catheter Nasogastric tube The NG tu...
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Neonatal respiratory distress (causes)

Causes of neonatal distress can be broadly split into intrathoracic, extrathoracic and systemic: Intrathoracic Medical respiratory distress syndrome (RDS) transient tachypnea of the newborn (TTN) meconium aspiration syndrome bronchopulmonary dysplasia (BPD) patent ductus arteriosus (PDA) ...
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Neuroblastic tumors

Neuroblastic tumors arise from primitive cells of the sympathetic system and include the following entities: neuroblastoma ganglioneuroblastoma ganglioneuroma These entities represent a spectrum of disease from undifferentiated and aggressive (neuroblastoma) to the well differentiated and la...
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Neuroblastoma vs Wilms tumor

Both neuroblastoma and Wilms tumor occur in early childhood and typically present as large abdominal masses closely related to the kidneys. Distinguishing between the two is important, and a number of features are helpful. Neuroblastoma calcification very common: 90% encases vascular structur...
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Non-accidental injury

Non-accidental injuries (NAI) represent both ethical and legal challenges to treating physicians. Radiologists may be the first clinical staff to suspect non-accidental injuries when confronted with a particular injury pattern. Knowledge of these is essential if the opportunity to save a child ...
Article

Odontohypophosphatasia

Odontohypophosphatasia is the mildest form of hypophosphatasia that manifests as tooth dysplasia and/or early loss of deciduous or permanent teeth. Pathology As with all forms of hypophosphatasia, the underlying abnormality is a mutation in the ALPL gene that encodes for tissue non-specific al...
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Pediatric cervical lesions (differential)

The differential diagnosis of pediatric cervical lesions is commonly encountered in practice, unfortunately, the list is long. Differential diagnosis Inflammatory Most lesions tend to be inflammatory 3: nontuberculous lymphadenitis scrofula sialodochitis abscess infected branchial cleft...
Article

Pediatric clavicle abnormalities

The clavicle is a unique bone and as such it often displays unique pathology. The following is an attempt to summarize pediatric clavicle abnormalities. Pediatric bone tumors and tumor-like lesions of the clavicle majority of clavicular tumors are malignant Ewing sarcoma (most common) osteos...
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Pediatric nasal cavity masses

Pediatric nasal cavity masses can occur within the nose or the nasopharynx. These masses are often found incidentally on imaging but can be readily apparent clinically. Clinical presentation The clinical features of these lesions tend to mimic upper respiratory processes and may result in dela...
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Pediatric renal tumors and masses

Pediatric renal tumors and masses are another group of diseases (just like cystic renal diseases in both the adult and child) that are bewildering in their number, nomenclature and overlapping findings. Commoner lesions Wilms tumor: common in older children 1-8 years old nephroblastomatosis: ...
Article

Pediatric skeletal metasases (differential)

There is a wide range of primary malignancies that results in pediatric skeletal metastases 1: neuroblastoma leukemia: although not truly metastases lymphoma clear cell sarcoma: Wilms’ variant rhabdomyosarcoma retinoblastoma Ewing’s sarcoma: lung metastases much more common osteosarcoma:...
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Patterns of neonatal hypoxic–ischemic brain injury

Neonatal hypoxic ischemic brain injuries can manifest in different patterns of involvement depending on the severity and timing of the insult. When considering the perinatal maturation process of the brain and the severity of an insult, it is possible to understand the various manifestations. T...
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Periosteal new bone formation in children

Periosteal reaction in the pediatric population, also known as periostitis in children, is relatively common occurrence and can result from many causes. Differential diagnosis The differential diagnosis for multiple bone periostitis include but not limited to the following: physiological peri...
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Pneumatosis coli

Pneumatosis coli is a descriptive sign presenting radiographically as intramural gas limited to the colonic wall.  Terminology There are different terminologies in the medical literature, such as pneumatosis intestinalis, pneumatosis coli, and pneumatosis cystoides intestinalis. Pneumatosis in...
Article

Posterior fossa astrocytoma

Posterior fossa astrocytomas, those arising either from the cerebellum or from the brainstem are most frequently seen in children. Approximately 60% of all pediatric astrocytomas are found in the posterior fossa (20% brainstem, 40% cerebellum). Many types of astrocytoma are found in the posteri...
Article

Pott shunt

A Pott shunt is a form of palliative surgery performed in patients with tetralogy of Fallot prior to the ability to repair the defect. It consists of a shunt formed between the descending thoracic aorta and the left pulmonary artery. This does not relieve the right ventricular outflow obstructi...
Article

Pre-axial polydactyly

Pre-axial polydactyly refers to polydactyly where the additional digit is towards the first digit of the hand (radial side) or foot (medially). Epidemiology Pre-axial polydactyly is less common than post-axial polydactyly, with an estimated incidence of 1 in 7000. Pathology Associations Pre...
Article

Premature closure of a growth plate (differential)

Premature closure of a growth plate subsequently results in a shortened bone, which can occur in a number of situations.  Pathology Common etiologies local hyperemia infection: osteomyelitis juvenile chronic arthritis juvenile rheumatoid arthritis hemophilia arteriovenous malformation t...
Article

Rachitic rosary

Rachitic rosary refers to expansion of the anterior rib ends at the costochondral junctions and is most frequently seen in rickets as nodularity at the costochondral junctions. Differential diagnosis Other causes of this appearance include:  scurvy the costochondral junction is more angular ...
Article

RASopathy

RASopathies are a class of developmental disorders caused by germline mutations in genes that encode for components or regulators of the Ras/mitogen-activated protein kinase (MAPK) pathway. Epidemiology As a group, RASopathies represent one of the most common malformation syndromes, with an in...
Article

Scalp hematoma

A scalp hematoma usually occurs following an injury at delivery although they are commonly seen with head trauma. Classification There are three types of hematoma, which are defined by their location within the scalp, particular their location as related to the galea aponeurosis and skull peri...
Article

Scham sign (hip)

The Scham sign of slipped capital femoral epiphysis is one of the subtle signs that may be seen on the AP view of an adolescent hip with early slip. In the normal adolescent hip, an intraarticular portion of the diaphysis of the collum overlies the posterior wall of the acetabulum inferiomedial...
Article

Sclerosing bone dysplasias

Sclerosing bone dysplasias comprise a heterogeneous group of disorders (skeletal dysplasias) united by the presence of sclerosis of one form or another. Some of these entities are thought to be related (e.g. osteopoikilosis, melorheostosis and Buschke-Ollendorff syndrome) 1.  They include: cra...
Article

Scoliosis

Scoliosis is defined as an abnormal lateral curvature of the spine. It is quite common in young individuals and is often idiopathic and asymptomatic. In some cases, however, it is the result of underlying structural or neurological abnormalities.  Terminology By definition, scoliosis is any la...
Article

Short limb skeletal dysplasia

Short limb skeletal dysplasias are skeletal dysplasias which are characterized by limb shortening Classification Rhizomelic (proximal limb shortening) hypochondroplasia achondroplasia chondrodysplasia punctata pseudoachondroplasia thanatophoric dysplasia particularly type II kyphomelic...
Article

Sincipital encephalocele

Sincipital encephaloceles are congenital herniations of cerebral parenchyma through a cranial defect. There are three main types 1,2: frontonasal encephalocele (~50%): more common in Asia and Latin America 4 naso-ethmoidal encephalocele (30%): more common in North America 4 naso-orbital (naso...
Article

Skeletal dysplasia

Skeletal dysplasia (also known as osteochondrodysplasia) refers to any abnormality in bone formation. There is a very wide clinicopathological spectrum and any part of the skeleton can be affected. Epidemiology The overall prevalence is estimated at ~2 per 10,000 live births 3. Pathology Typ...
Article

Solitary sclerotic bone lesion

The differential diagnosis of a solitary sclerotic bone lesion is heavily influenced by the age of the patient, and includes: sclerotic metastasis solitary either because no others are present or no others have been imaged enostosis (bone island) osteosarcoma calcifying enchondroma osteobl...
Article

Spinal Dysraphism

Spinal dysraphism is a broad term given to a group of anomalies where there are malformations in the dorsum of the embryo. Neural tube defects come under this group as well.  Pathology The neural tube is formed by the lengthwise closure of the neural plate, in the dorsum of the embryo. The up...
Article

Stroke in children and young adults

Brain ischemia/infarction in children and young adults can result from several causes. embolic phenomena cyanotic heart disease cardiomyopathies mitral valve prolapse Osler-Weber-Rendu syndrome arterial dissection trauma spontaneous fibromuscular dysplasia Marfan syndrome Ehlers Danlo...
Article

Syndactyly

Syndactyly (plural: syndactylies) refers to a congenital fusion of two or more digits. It may be confined to soft tissue (soft tissue syndactyly/simple syndactyly) or may involve bone (bony syndactyly/complex syndactyly). Epidemiology The overall estimated incidence is at ~1 per 2,500 to 5,000...

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