Fuortes Michaelangelo, Vijapura Charmi, Dennhardt Joel, Policeni Bruno, Sato Yutaka, Sato T Shawn
Final Pr. ID: Poster #: EDU-104
1) Review the normal development and anatomy of the middle cranial fossa.
2) Describe the variety of pathologies affecting the middle cranial fossa in the pediatric age group with a focus on the typical computed tomography (CT) and magnetic resonance imaging (MRI) characteristics.
3) Discuss clinical management and imaging follow up of middle cranial fossa pathology.
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Authors: Fuortes Michaelangelo , Vijapura Charmi , Dennhardt Joel , Policeni Bruno , Sato Yutaka , Sato T Shawn
Keywords: skull base anatomy, skull base pathology, middle cranial fossa
Dennhardt Joel, Fuortes Michaelangelo, Vijapura Charmi, Policeni Bruno, Sato Yutaka, Sato T Shawn
Final Pr. ID: Poster #: EDU-089
1) Review the normal development and anatomy of the posterior skull base.
2) Describe the variety of pathologies affecting the posterior cranial fossa in the pediatric age group with a focus on the typical computed tomography (CT) and magnetic resonance imaging (MRI) characteristics.
3) Discuss clinical management and imaging follow up of posterior cranial fossa pathology.
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Authors: Dennhardt Joel , Fuortes Michaelangelo , Vijapura Charmi , Policeni Bruno , Sato Yutaka , Sato T Shawn
Keywords: Skull base, Posterior Cranial Fossa, Magnetic resonance imaging
Masum Rukya, Dixon Chanae, Ryan Maura, Jaju Alok
Final Pr. ID: Poster #: EDU-067
This review describes the CT and MRI features of developmental variants and pathological lesions that involve the skull base, excluding those centered in the nasal cavity, nasopharynx, sinuses and orbits.
Normal anatomy of developing bony skull base will be illustrated. The lesions are categorized by pathology rather than locations, and the following entities will be covered.
Congenital and developmental lesions - arrested pneumatization, aberrant arachnoid granulations, dermoid/epidermoid cysts, ecchordosis physaliphora, encephaloceles, persistent craniopharyngeal canal
Inflammatory/Infectious lesions - skull base osteomyelitis, petrous apicitis, cholesterol granuloma
Benign lesions - Fibrous dysplasia, aneurysmal bone cyst, osteoma, osteochondroma, meningioma
Malignant lesions - Langerhans cell histiocytosis, lymphoma, neuroblastoma metastasis, Ewing’s sarcoma, osteosarcoma, chordoma, chondrosarcoma
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Authors: Masum Rukya , Dixon Chanae , Ryan Maura , Jaju Alok
Keywords: Skull base, Pediatrics, skull base lesion
Hammer Matthew, Shukla Neal, Kim Joseph, Hajibeygi Ramtin, Lozano Richard, Tu Long
Final Pr. ID: Poster #: CR-040
Gorham-Stout disease is an osteolytic bone disorder associated with abnormal lymphangiogenesis. The disease commonly involves the ribs, cranium, clavicles, and cervical spine; however, it may be seen anywhere throughout the skeleton. The disease has variable inheritance, has no known markers, does not exhibit a predilection for sex or race, and may present at any age, although it is usually diagnosed in adolescence. Gorham-Stout remains an exceedingly rare disease with only 300 reported cases in the literature.
Our patient is a 15-month-old, previously healthy child that presented with fevers and a seizure. CT head without contrast showed uncomplicated otitis media, and patient was appropriately treated and discharged. 4 months later, a follow up MRI brain with and without contrast was obtained for continued lethargy, poor oral intake, and right-sided slowing on EEG. Results showed fluid-filled polyostotic lesions within the right petrous bone and clivus with dehiscence along the posterior petrous bone. Given the polyostotic lesions without intervening inflammatory reaction, the diagnosis of Gorham-Stout was suspected. A subsequent bone survey did not reveal additional lesions. Follow up MRI imaging showed interval development of right cervical neck cystic spaces from petrous bone CSF leak, bilateral subdural effusions, and elevated intracranial pressures requiring ventriculoperitoneal shunt placement. On CT myelogram, a right pars nervosa meningocele was found, thought to be secondary to the above process.
Gorham-Stout remains an elusive disease that is difficult to diagnose as it has no known genetic precursors or associations. It exhibits variable phenotypic presentation, as in this case where it was seen in a 15-month-old child rather than at adolescence, with severe neurologic sequela from skull base lesions. The superimposed otitis media created an interesting diagnostic dilemma as the middle ear fluid was originally thought to represent an uncomplicated acute infection; it is unclear if the underlying disease process predisposed the patient to infection given the static fluid accumulation. Although typically a diagnosis of exclusion, Gorham-Stout should remain in the differential as timely identification of the disease will allow for more targeted management that can minimize osseous demineralization and potential sequela of disease.
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Authors: Hammer Matthew , Shukla Neal , Kim Joseph , Hajibeygi Ramtin , Lozano Richard , Tu Long
Keywords: Other, Skull Base Lesion
Final Pr. ID: Poster #: CR-067
The purpose of this case report is to describe a rare case of epignathus (oral teratoma) with lateral skull base and intracranial extension. A 29-year-old G4P1122 female was referred to our institutuion after third trimester ultrasound and fetal MRI revealed a 34 week fetus with oral mass. There was extension intracranially through the lateral skull base. The complex mass showed cystic, solid, and fatty components. Polyhydramnios was also demonstrated. The prenatal imaging was crucial in planning the delivery of the fetus using EXIT procedure. Postnatal MRI Head and Neck, CT Head and Neck, CTA Head and Neck were helpful in guiding surgical resection of the oral, skull base, and intracranial mass. Emphasis will be made on the value of imaging to guide the management of this extremely difficult and rare case. Read More
Authors: Leake David
Keywords: epignathus, teratoma, Fetal MRI, Skull Base