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Biomedical subjects

J H Hise

Publications and source records attributed to J H Hise.

8 recordsLinked to original sources
PubMed1996

MR imaging of Creutzfeldt-Jakob disease.

PURPOSE: To describe the magnetic resonance (MR) imaging appearance of Creutzfeldt-Jakob disease (CJD). MATERIALS AND METHODS: MR images obtained in 29 patients who died of CJD (aged 53-77 years at death) were retrospectively reviewed by three neuroradiologists blinded to the diagnosis. RESULTS: Moderate to marked bilateral, symmetrically increased signal intensity was demonstrated in the putamen and caudate nucleus on T2- and proton-density-weighted MR images in 23 patients (79%). In six patients (21%), images showed no major signal intensity abnormalities. T1-weighted images revealed no signal intensity abnormalities and no contrast material enhancement. The degree of atrophy in the cortex and basal ganglia corresponded to the time between onset of symptoms and MR imaging. All patients with a disease duration of longer than 4 months had substantial volume loss. CONCLUSION: Although approximately 20% of the patients did not have MR imaging abnormalities, MR imaging did show signal intensity alterations due to gliosis and spongiform changes early in the course of CJD in the remaining 80%. The demonstration of bilateral areas of increased signal intensity that predominantly affected the caudate nuclei and the putamina on long-repetition-time MR images in an elderly patient with rapidly progressive dementia represents a specific finding and clearly should suggest the diagnosis of CJD.

Aged↗
PubMed1994

Partial development of the corpus callosum.

PURPOSE: To determine whether the MR findings of callosal dysgenesis suggest that the partially formed corpus callosum in humans is the result of arrested growth or delayed continued development. METHODS: The MR scans of 25 patients with callosal dysgenesis were reviewed to determine whether the observed corpus callosum corresponded to the form and position of a portion of a normal corpus callosum, as suggested by a theory of arrested growth. RESULTS: In 10 of the 25 cases, the partially formed corpus callosum corresponded to a portion of a normal corpus callosum. In the remaining 15 cases, the partially formed corpus callosum was located posterior to the expected location of a normal genu and inferior to the expected location of a normal body. CONCLUSIONS: Corpus callosum dysgenesis in humans may be caused by arrested growth in some cases; in other cases it is most likely caused by delayed continued development that attempts to compensate for earlier abnormalities in the evolution of midline structures.

Abnormalities, Multiple↗
PubMedDate not supplied

Intracranial granulocytic sarcoma: CT, MR, and angiography.

Granulocytic sarcoma is a rare, solid tumor composed of immature granulocytes usually found in association with systemic leukemia in younger patients. We present a case of granulocytic sarcoma occurring in an elderly female with no evidence of systemic leukemia. Computed tomography, MR (with and without Gd-DTPA), and angiography showed features commonly found in meningiomas.

Aged↗
PubMedDate not supplied

Gliosarcoma: MR features.

PURPOSE: Our goal was to characterize the MR features of pathologically documented gliosarcoma and to determine if these features help differentiate gliosarcoma from other intracranial neoplasms. METHOD: MR studies of six patients with pathologically documented gliosarcoma were retrospectively analyzed. RESULTS: The tumors tended to be well defined lesions demonstrating either an inhomogeneous or cystic appearance with surrounding vasogenic edema. All tumors were characterized as primarily intraaxial but abutting a dural surface. On T2-weighted images, all tumors were of intermediate signal intensity with surrounding edema. The signal intensity of the tumor was similar to gray matter but was hypointense relative to other glial neoplasms. Postcontrast T1-weighted images showed intense tumor enhancement, often with a ring-like appearance. The isointense component on the T2-weighted images corresponded to this area of intense enhancement. CONCLUSION: Gliosarcoma exhibits some characteristic MR features. It should be included in the differential diagnosis of any tumor that appears to be intraaxial but abuts a dural surface and is much less hypointense on T2-weighted images than other glial neoplasms.

Adult↗
PubMedDate not supplied

Stroke associated with coronary artery bypass surgery.

Medical records and neuroimaging studies of 30 patients with major neurologic events after coronary artery surgery were reviewed. Two thousand and twenty-nine coronary artery bypass graft operations were performed in our institution between October 15, 1985, and December 27, 1989. Of these, there were 30 documented neurologic events suggesting acute ischemic injury during the intraoperative or the postoperative period. Clinical manifestations included hemiparesis, monoparesis, aphasia, bilateral cortical dysfunction, cortical and brainstem dysfunction, and left homonymous hemianopsia. There were five deaths directly attributable to neurologic injury. Twenty-two patients had a CT scan of the head, of which 15 showed evidence of acute infarction, two suggested watershed lesions from cerebral hypoperfusion, and the remainder showed findings consistent with multiple cerebral emboli or primary intracranial occlusion. Five carotid arteriograms and one digital subtraction arteriogram of the carotids were obtained. Angiographic findings revealed two common carotid artery occlusions, one callosal marginal artery occlusion, and two cases of bilateral high-grade internal carotid stenoses. Our findings support the contention that in patients who suffer cerebral infarction associated with coronary artery bypass grafting, the main mechanism of injury is cerebral embolization rather than cerebral hypoperfusion.

Aged↗
PubMedDate not supplied

Intraventricular fibroma: MR and pathologic comparison.

This case report describes clinical, surgical, MR, and pathologic findings of an intraventricular fibroma, a rare, benign mesenchymal neoplasm. Relatively isointense with normal brain parenchyma on T1-weighted images, the tumor exhibited hyperintense signal on T2-weighted pulse sequences and enhanced intensely and homogeneously after intravenous administration of gadopentetate dimeglumine. Choroid plexus papilloma/carcinoma, meningioma, ependymoma, and subependymal giant cell astrocytoma should be included in the differential diagnosis.

Cerebral Ventricle Neoplasms↗