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Teenager with left orbital and forehead swelling

CT of Pott puffy tumor and subdural empyema
Sagittal CT with contrast of the brain shows frontal and left maxillary sinusitis and extensive soft tissue swelling anterior to the forehead (upper left) and destruction of the anterior left frontal bone in the frontal sinus and extensive soft tissue swelling anterior to the left orbit (upper right). Coronal (lower left) and sagittal (lower right) T1 MRI with contrast of the brain shows diffuse meningeal enhancement, subdural empyemas along the falx and both cerebral convexities, and multiple large non-enhancing subgaleal fluid collections in the left scalp.

The diagnosis was meningitis, subdural empyema, and Pott puffy tumor as complications of sinusitis.

School ager who does not take care of their teeth and had a seizure

MRI of intracranial abscess due to sinusitis
Axial T2 MRI of the brain (above left) shows a mass in the right front lobe with surrounding vasogenic edema. Axial (above right) and coronal (below right) T1 MRI with contrast shows the mass to have thin rim enhancement and the coronal image also shows left maxillary sinusitis. The mass is shown to demonstrate diffusion restriction on diffusion-weighted imaging (below left).

The diagnosis was intracranial abscess as a complication of sinusitis.

Toddler with stridor since birth

Surgical image of right aortic arch with aberrant left subclavian artery
Surgical image taken through a left thoracotomy shows a blue vessel loop around the ligamentum arteriosum which was compressing the esophagus posterior to it. The red vessel loops are around the right aortic arch (on the right) and the left subclavian artery (on the left). The vascular ring was subsequently divided by division of the ligamentum arteriosum. The vascular ring then sprang open dramatically, relieving its compression upon the esophagus.

The diagnosis was right aortic arch with aberrant left subclavian artery and ligamentum arteriosum forming an incomplete vascular ring.

School ager with seizures

MRI of perisylvian polymicrogyria and open lip schizencephaly
Coronal and axial T1 (above) and axial T2 (below) MRI without contrast of the brain shows small haphazard appearing gyri and too few sulci present bilaterally, left greater than right, primarily in the sylvian fissures. There is also a cleft of gray matter with cerebrospinal fluid within extending from the cortex to the posterior aspect of the left lateral ventricle.

The diagnosis was polymicrogyria in a patient with left open lip schizencephaly.

Infant with meningomyelocele who has had a VP shunt placed

MRI of heterotopia
Axial (left) and coronal (right) T2 MRI without contrast of the brain shows multiple subependymal nodules along the lateral wall of the left lateral ventricle that have signal characteristics similar to those of gray matter. Similar lesions were found in the right lateral ventricle on images that did not contain artifact from the right parietal VP shunt.

The diagnosis was heterotopia.

Infant with choking with feeding

Surgical image through a thoracotomy incision (left) shows blue vessel loop around an aberrant left subclavian artery arising from a Kommerell diverticulum. Black suture loop is around a patent ductus arteriosus that was noted to extend from the Kommerell diverticulum and completed a vascular ring which was compressing the esophagus posterior to it. Surgical image (right) with the patent ductus arteriosus mobilized off the esophagus which is between the tips of the hemostat show the esophagus now resorting to its normal caliber.

The diagnosis was right aortic arch with aberrant left subclavian artery and patent ductus arteriosus forming a complete vascular ring.

Toddler with seizures

MRI of tuberous sclerosis
Axial T2 MRI without contrast of the brain (left) shows three rounded low intensity subependymal lesions along the lateral aspect of the left lateral ventricle. Axial FLAIR MRI image without contrast of the brain (right) shows multiple bilateral poorly defined hyperintense areas located just beneath the cortex of the brain.

The diagnosis was multiple subependymal nodules and subcortical tubers in tuberous sclerosis.

Preschooler with cafe au lait spots

MRA of Moya Moya syndrome in neurofibromatosis type I
AP view of a 3D maximum intensity projection of an MRA of the neck with contrast (above) and AP (below left) and inferior (below right) views of a 3D maximum intensity projection of an MRA of the brain without contrast shows diffuse hypoplasia of the left internal carotid artery. There is stenosis and occlusion of the cavernous and supraclinoid segments of the left internal carotid artery and then there is a thin left M1 segment without evidence of collaterals in the basal ganglia. Additionally, aneurysms are noted in the left A1 and A2 segments.

The diagnosis was Moya Moya syndrome in a patient with neurofibromatosis type I.