School ager with an abdominal wall mass after blunt trauma to the anterior abdominal wall

MRI of intramuscular hematoma associated with a lymphatic malformation of the anterior abdominal wall
Axial T1 without contrast (above), T2 (middle) and T2 with fat saturation (below) MRI of the abdomen shows an oval heterogenous fluid collection of layering mixed fluid intensities centered in the right anterior abdominal wall muscle and surrounded by muscle tissue.

The diagnosis was intramuscular hematoma associated with a lymphatic malformation of the anterior abdominal wall.

Teenager after motor vehicle accident

CT of Type 2 fracture of the odontoid process of the C2 vertebral body and atlanto-occipital dissociation
Midline sagittal CT without contrast of the cervical spine (middle) shows a transverse comminuted fragmented fracture through the C2 vertebral body. There is anterior displacement of the C1 vertebral body resulting in compromise of the spinal canal. There is massive thickening of the retropharyngeal soft tissues due to a retropharyngeal hematoma. The basion-dens interval is abnormally increased. The off midline sagittal CTs (left and right) show distraction between the occipital condyles bilaterally and the C1 articular facets.

The diagnosis was a Type 2 fracture of the odontoid process of the C2 vertebral body and atlanto-occipital dissociation.

Premature newborn with respiratory distress

CXR of symmetrical distribution of artificial surfactant in a patient with respiratory distress syndrome
CXR AP obtained just after birth (above left) shows the lungs bilaterally to be relatively clear and hypoexpanded. CXR obtained 4 hours later after intubation (above right) shows interval development of bilateral symmetrical ground glass opacity in the lungs which remain hypoexpanded. CXR obtained 4 hours after the administration of artificial surfactant (below) shows the lungs now to be normally expanded and to be clear of the previously seen ground glass opacities.

The diagnosis was respiratory distress syndrome before and after the symmetrical administration of artificial surfactant.

Premature newborn with gastrointestinal bleeding after replacement of the nasogastric tube

AXR of nasogastric tube causing gastric perforation
Baseline CXR AP obtained yesterday (left) shows a nasogastric tube coursing through the esophagus and then curving towards the stomach on the left side of the abdomen. AXR AP after nasogastric tube replacement (right) shows a straight course to the newly placed nasogastric tube whose tip projects in the midline at the level of the L3 vertebral body. There is a faint oval lucency in the midline of the upper abdomen at the level of the T10 and T11 vertebral bodies.

The diagnosis was nasogastric tube malfunction in the form of gastric perforation caused by placement of a nasogastric tube resulting in pneumoperitoneum.

Newborn with one perineal opening for the vagina and urethra and rectum

Fluoroscopic exam of cloacal malformation
AP (above left) and lateral (above right) images during injection of water soluble contrast into the vagina shows a dilated vagina and a duplicated uterus. Lateral image during antegrade injection of water soluble contrast into the patient’s distal mucous fistula (below left) shows a connection between the posteriorly located distal rectum and the posterior aspect of the vagina. Lateral image obtained during filling of the anteriorly located bladder with water soluble contrast through a suprapubic catheter (below right) shows the proximal urethra just inferior to the bladder to be dilated.

The diagnosis was cloacal malformation.

Infant with abdominal pain

AXR of CT of pneumatosis intestinalis of the colon
AXR AP (above left) shows extensive curvilinear air throughout the wall of the colon from the cecum to the rectum. There is contrast in the bladder from the contemporaneously performed CT. Axial (above right) and coronal (below) CT with contrast of the abdomen show a large amount of air in the wall of the colon throughout the entire colon.

The diagnosis was pneumatosis intestinalis of the entire colon of unknown etiology.

Newborn who experienced oligohydramnios in utero

CXR and US of autosomal recessive polycystic kidney disease causing oligohydramnios and pulmonary hypoplasia
CXR AP (above) shows a small bell-shaped thorax with poorly expanded lungs despite being on a ventilator. Transverse US of the left kidney (below left) and right kidney (below right) shows the kidneys bilaterally to be enlarged and to be composed of innumerable microcysts giving the kidneys overall an echogenic appearance.

The diagnosis was autosomal recessive polycystic kidney disease resulting in oligohydramnios resulting in pulmonary hypoplasia.