Glioblastoma Presenting with Acute Middle Cerebral Artery Territory Infarct.

Acute ischemic stroke caused by a malignant mass has been described in the literature in few case reports. We describe an unusual case of acute ischemic middle cerebral artery distribution infarction secondary to glioblastoma.

The use of cephalometric landmarks with 3-dimensional volumetric computer modeling to position an auricular implant surgical template: a clinical report.

The number of tools available to make a correctly positioned surgical guide for auricular implant placement is rapidly expanding as advances in 3-dimensional computer modeling continue. While the correct orientation of a missing auricle previously relied solely on soft tissue topography, computer modeling software now allows for navigational viewing of hard tissue and cephalometric landmarks. This clinical report describes a technique to establish the orientation of an auricular surgical guide incorporating the use of fundamental cephalometry. Cephalometry as a treatment planning tool has been limited to orthodontics and maxillofacial surgery. This article describes its use in a patient with a missing ear.

Balamuthia mandrillaris meningoencephalitis associated with solid organ transplantation--review of cases.

We report the first identified transmission of Balamuthia mandrillaris through solid organ transplantation. Kidneys were transplanted from a donor with presumptive diagnosis of autoimmune encephalitis. Shortly after, the recipients developed neurologic symptoms. Magnetic Resonance Imaging of the brain from the donor and both kidney recipients demonstrated multiple ring enhancing lesions with surrounding edema and adjacent leptomeningeal extension. In addition most of the lesions demonstrated signal changes suggesting central hemorrhagic foci. Specimens were tested locally and at the Centers for Disease Control and Prevention. Histopathology revealed B. mandrillaris in either brain tissue and/or cerebral spinal fluid in the donor and recipients.

Differentiation of neuromyelitis optica from multiple sclerosis on spinal magnetic resonance imaging.

In order to examine the accuracy of magnetic resonance imaging (MRI)-based diagnosis of neuromyelitis optica (NMO) versus multiple sclerosis (MS), we performed a retrospective, rater-blinded review of 29 cases of NMO and 30 cases of MS using the criteria of long (more than three vertebral levels), continuous lesions with a central cord location for NMO and more peripheral and patchy lesions for MS. Using these criteria, two raters were able to distinguish the two conditions with a good degree of confidence, particularly when the imaging was performed at the time of an acute cord attack. The sensitivity and specificity for diagnosis of NMO were 86.2% and 93.3%, respectively, for Rater A and 96.4% and 78.6%, respectively, for Rater B, with a kappa value of 0.72. Thus there are significant differences in lesion characteristics that allow the distinction on spinal cord imaging between MS and NMO with a moderately high degree of confidence. The location of the lesion as evident on MRI of the spine can be regarded as a distinguishing diagnostic feature between MS and NMO.

Hypertrophic olivary degeneration after resection of a pontine cavernous malformation: a case report.

We report the case of a 35 year old African American female who developed hypertrophic olivary degeneration secondary to resection of a pontine cavernous malformation. The patient initially complained of headaches and diplopia. Unenhanced computed tomography (CT) and magnetic resonance images (MRI) of the brain revealed a left pontine cavernous malformation with scattered foci of recent and remote hemorrhage. The patient subsequently underwent surgical resection of the lesion. Follow up MRI 7 months post surgery demonstrated hypertrophy and T2 signal hyperintensity in the ipsilateral inferior olivary nucleus secondary to hypertrophic olivary degeneration. Familiarity with this diagnosis and its imaging characteristics is required of the radiologist to prevent erroneous diagnoses of other pathology.

Giant recurrent glomus jugulotympanicum with intracranial, extracranial, and nasophayngeal extension: The imaging role in clinical management.

We present a 50-year-old male with a massive glomus jugulotympanicum that demonstrated extracranial extension breaking through the skin in the posterior auricular region, intracranial extension into the middle cranial fossa, and nasopharyngeal extension involving the entire length of the eustachian tube. Characteristic CT, MR, angiographic, and pathologic findings are demonstrated in this case. The difficult decision regarding treatment options must be made with careful consideration of the associated morbidities of slow tumor growth and recurrence with conservative management versus the surgical morbidities of aggressive surgical resection. Imaging is arguably the most important component of this decision-making process, with the radiologist contributing significantly to multiple aspects of the management of glomus tumors.