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Biomedical subjects

J L Sherman

Publications and source records attributed to J L Sherman.

At least 19 recordsLinked to original sources
PubMed1992

CT and MR imaging of the pediatric orbit.

Orbital abnormalities encountered in the pediatric population differ substantially from those found in adult patients. Retinoblastoma, the most serious intraocular tumor, is often difficult to diagnose, but use of computed tomography (CT) (which reveals the characteristic focal calcification) and magnetic resonance (MR) imaging allows this tumor to be differentiated from pseudogliomas, such as Coats disease, and retrolental fibroplasia. CT and MR imaging help in the differentiation of orbital cellulitis from preseptal, lacrimal, and eyelid infectious processes and of orbital pseudotumor from Graves disease. In cases of orbital trauma, CT is excellent for detecting orbital fractures and metallic foreign bodies; MR imaging is better for depicting ocular and optic nerve injuries. Both modalities allow the differentiation of rhabdomyosarcoma from dermoid, cavernous hemangioma, and lymphangioma and provide helpful information for the diagnosis of many other tumors. Since CT and MR imaging have widely expanded the capabilities of orbital imaging, it is more important than ever before for radiologists to understand pediatric orbital disease.

Eye Abnormalities↗
PubMed1990

NIH conference. Neurofibromatosis 1 (Recklinghausen disease) and neurofibromatosis 2 (bilateral acoustic neurofibromatosis). An update.

The neurofibromatoses comprise at least two autosomal dominant disorders affecting an estimated 100,000 Americans with clinical manifestations that may require care from every type of clinician. Neurofibromatosis 1 and neurofibromatosis 2 have in common the occurrence of many neurofibromas but are distinctly different clinical disorders. The disease genes are on different chromosomes. Magnetic resonance imaging, particularly with gadolinium enhancement, has generally supplanted other techniques for visualizing brain, spinal, and other neural tumors in both disorders. The technique has rekindled the controversy over the nature and frequency of optic pathway tumors in patients with neurofibromatosis 1 and has revealed, throughout the brains of young patients, bright lesions that have uncertain clinical consequences and unknown pathologic bases. In patients with neurofibromatosis 2, small acoustic neuromas can be seen, leading to the possibility of excision with preservation of hearing and facial nerve function. Abnormal hearing may occur to excess in patients with neurofibromatosis 1, but acoustic neuroma has never been documented. In patients with neurofibromatosis 2, a battery of audiologic tests has a high positive predictive power. Lisch nodules or iris hamartomas, probably a universal sign in adults with the neurofibromatosis 1 gene, cause no problem with vision. Posterior capsular lens opacity in patients with neurofibromatosis 2 is a helpful diagnostic sign and a potential source of additional handicap in persons at risk for impaired hearing. Progress in the clinical delineation of the disorders has been matched with considerable research into the still obscure pathogenesis of the disorders. Such rapid advances may necessitate reconsideration of the conclusions of the National Institutes of Health Consensus Development Conference on Neurofibromatosis, especially those on the categories of persons in which a neurofibromatosis should be considered and the need for caution in recommending surgery. Watchful waiting may often be the best management for acoustic neuromas in neurofibromatosis 2.

Chromosome Aberrations↗
PubMed1990

MRI and neuropsychological correlates of dementia in Binswanger's disease.

Nuclear magnetic resonance imaging (MRI) has facilitated diagnosis of Binswanger's disease in vivo, which has proven to be a more common disease entity than once believed. These patients generally present with hypertension, progressive dementia, hydrocephalus, gait difficulty, and personality change. A patient is presented with MRI findings of white-matter destruction and subcortical lesions, and with neuropsychological findings of higher-order cognitive impairment but selectively preserved language and visuospatial-perceptual skills. The relationship between the patient's cognitive-behavioral symptoms and the presence of disconnection syndrome is discussed. In addition, the utility of neuropsychological examination is reviewed. Finally, implications for differentiating cortical from subcortical dementia with psychometric test data are discussed.

Journal Article↗
PubMed1990

MR imaging of CSF-like choroidal fissure and parenchymal cysts of the brain.

The purposes of this study were to delineate the MR characteristics of CSF-like parenchymal or fissural cysts of the brain and to correlate them with the clinical findings. Clinical data and MR images of 34 patients with these abnormalities were reviewed. Pathologic correlation was not available. Two types of cystic lesions were identified and separated by location: medial temporal lobe cysts arising in or near the choroidal fissure (26 patients) and parenchymal or pseudoparenchymal cysts not related to the choroidal fissure (eight patients). The choroidal fissure cysts simulated intraparenchymal cysts on axial images but their extraaxial location was well portrayed on the coronal images. Choroidal fissure cysts had a characteristic spindle shape on sagittal images. The other cysts were found in the temporal lobe (seven patients) or thalamus (one patient) and appeared parenchymal but situated close to the subarachnoid space. These lesions were round or ovoid. There was no abnormal enhancement in 10 patients studied with gadopentetate dimeglumine. Coronal images were most useful, revealing the cysts as focal CSF-intensity lesions expanding the choroidal fissure of the temporal lobe. All the cysts appeared to represent incidental findings that did not correlate with the clinical signs and/or symptoms that prompted the imaging evaluations. The MR characteristics of CSF-like cysts are important to recognize so that they are not confused with other, more serious entities, such as intraaxial cystic tumors, infarctions, or parasitic lesions.

Adolescent↗
PubMed1990

Sarcoidosis of the CNS: comparison of unenhanced and enhanced MR images.

Sarcoidosis involving the CNS has a predilection for the leptomeninges, although parenchymal involvement occurs. We retrospectively evaluated the appearance of CNS sarcoidosis on unenhanced and enhanced MR images. MR studies were abnormal in 17 of 20 patients with CNS sarcoidosis. In all 17 patients, meningeal disease was detected on the gadopentetate-dimeglumine-enhanced T1-weighted images; the disease was detected on unenhanced images in three patients. Well-defined leptomeningeal patterns of enhancement were present in 15 patients. Other areas of involvement were the dura; brain parenchyma including hypothalamus, periventricular white matter, and ventricular ependyma; optic chiasm; and pituitary gland. Gadopentetate dimeglumine optimally evaluates meningeal disease and highlights the importance of the leptomeninges and Virchow-Robin spaces in the pathogenesis of CNS sarcoidosis. Enhanced MR is the preferred imaging technique for the evaluation of CNS sarcoidosis.

Adult↗
PubMed1989

The association of posterior capsular lens opacities with bilateral acoustic neuromas in patients with neurofibromatosis type 2.

This study of 47 patients from 11 families with neurofibromatosis type 2 (NF 2) confirms our previously reported association between posterior capsular cataract and NF 2. A highly significant statistical association was found between the presence of posterior capsular lens opacities and the presence of NF 2 as determined by magnetic resonance imaging or pathologic diagnosis. This association was not present for other types of lens opacities that could be the result of age-related or nonspecific changes. When considering the diagnosis of NF 2, this finding now makes it essential to use a careful dilated biomicroscopic examination of the lens to evaluate known, suspected, or at-risk individuals for this potentially early associated manifestation.

Cataract↗
PubMed1987

The variable anteroposterior position of the retroperitoneal colon to the kidneys.

Five hundred supine abdominal CT scans were reviewed retrospectively to determine the variation of colonic position about each kidney. The anteroposterior position of the retroperitoneal colon was evaluated for different age groups and sexes at the level of the upper-, mid-, and lower-renal poles. The ascending/descending colon generally assumed a more posterior position about the lower poles and left kidney vs. the upper poles and right kidney. There were few significant differences between the sexes and among different age groups with two exceptions. In middle-aged and older women, the descending colon lay more lateral to the left lower kidney than in their male counterparts. Second, although the colon was located behind the kidney (retrorenal colon), in a nearly equal number of men and women, most patients with this colonic position were 60 years of age or older and had it about their lower renal poles. The overall frequency of retrorenal colon in the supine patient was 1.9%.

Adolescent↗
PubMed1987

The retrorenal colon in the supine and prone patient.

Ninety patients underwent computed tomographic scanning in both the supine and prone positions to show the orientation of the retroperitoneal colon about the kidneys and allow evaluation of changes in colonic position and contents. The data were compared with data on 500 patients scanned only when supine. Particular attention was given to bowel found posterior to the kidneys (retrorenal colon): its frequency of occurrence on 500 scans of supine patients was 1.9%, but 10.0% in the 90 prone patients. Because most invasive renal procedures would not intersect with retrorenal colon located behind the lateral one-third of the kidney, the data were reevaluated after deletion of these patients, giving a frequency in prone patients of 4.7%. This was found exclusively at the level of the lower renal poles, and the involved colon was extensively distended with gas. Attention should be given at fluoroscopy to detect this unusual, posteriorly positioned, air-filled colon before any invasive renal procedure.

Adult↗
PubMed1987

The MR appearance of CSF flow in patients with ventriculomegaly.

The purpose of this study was to investigate the MR imaging appearance of mobile CSF in the ventricular system in patients with ventriculomegaly caused by brain atrophy and extraventricular obstructive hydrocephalus. Pulsatile CSF often has decreased intensity relative to less mobile areas of CSF, particularly on T2-weighted scans. At times, the flow-related signal dropout causes striking heterogeneity in the appearance of CSF. This has been termed the CSF flow-void sign (CFVS) and is most likely caused by spin-phase shifts and time-of-flight effects created as a result of CSF turbulence and increased velocity of CSF pulsatile flow. The effect is most pronounced in areas where a larger volume of CSF moves through a small channel or foramen, such as the aqueduct of Sylvius or foramen of Magendie. The scans of 40 patients with ventriculomegaly caused by brain atrophy or extraventricular obstructive hydrocephalus were reviewed for the presence of the CFVS. All patients had the CFVS in the aqueduct of Sylvius on T2-weighted spin-echo sequences. The sign was present in the fourth ventricle in 96%, in the third ventricle in 70%, in the foramen of Magendie in 65-77%, and in the foramina of Monro in 33%. The sign was more pronounced in patients with larger ventricles but could not be used to differentiate patients with brain atrophy from those with extraventricular obstructive hydrocephalus.

Adult↗
PubMed1987

Physiology of the CSF flow-void sign: modification by cardiac gating.

Low-intensity signal seen within areas of narrowing within the ventricular system has been termed the CSF flow-void sign. This decreased signal is related to CSF flow and turbulence. Seven normal volunteers were examined, and the changes that occurred in the appearance of the CFVS were noted when data acquisition was modified by cardiac gating. Flow-void patterns within the internal cerebral veins and basilar artery were also examined. The results of this study confirm that CSF flow is related to cardiac systole and diastole. An increase in hypointensity is seen in the areas of the aqueduct of Sylvius and the foramen of Magendie during the time at which the systemic arterial pulse wave is transmitted into the brain. The physiology of this observation is related either to a direct hydraulic effect of the venous system on the CSF or to filling and expansion of the thin-walled cerebral venous system. Hypointensity or an increase in the width of the basilar artery and internal cerebral veins during systolic data acquisition was also noted. The mechanism of this phenomenon is related to propagation of the systemic arterial pulse wave.

Cerebral Ventricles↗
PubMed1987

The MR appearance of syringomyelia: new observations.

Fifty-eight patients with spinal cord cavities were studied with MR imaging. Patients were separated into four groups, and the appearance of the cavities were compared. There were 24 patients (41.4%) with communicating syringomyelia (associated with the Chiari I malformation). Sixteen patients (27.6%) had posttraumatic syringomyelia, nine patients (15.5%) had associated tumors, and nine patients (15.5%) had idiopathic syringomyelia. The characteristics of each syrinx, the spinal cord, and the appearance of the cerebellar tonsils were analyzed on T2- and T1-weighted images. There is a striking similarity in the appearance of many syrinx cavities regardless of the cause. Characteristics that were found in some patients in every group included areas of increased intensity on T2-weighted images, the presence of the CSF flow-void sign (CFVS) in the syrinx cavity, eccentric cavities, "beaded" cavities, and cord enlargement. Tonsillar ectopia alone does not indicate that a syrinx is of the "communicating" type, since it was present in two of 16 patients (13%) with trauma and in two of five patients (40%) with tumors. T1-weighted images were most useful in evaluating the anatomic characteristics of the syrinx and the cerebellar tonsils. Most syrinx cavities involved the cervicothoracic junction. The average length was between five and nine vertebral segments (depending on category) but varied between one and 20 vertebral segments. T2-weighted images revealed areas of increased intensity in the spinal cord in 13 patients without tumors. Two of these cases were shown to represent gliosis on histopathologic review. The CFVS was present in the syrinx cavities of 23 patients (40%), probably reflecting pulsatile movements of the syrinx fluid. It has been proposed that such movements are a cause of syrinx propagation, and the observation of the CFVS may have prognostic significance. The development and progression of the CFVS was documented in serial MR examinations in one patient over an 18-month period. The theories of syrinx development and propagation are reviewed.

Adolescent↗
PubMed1987

MR and CT evaluation of intracranial sarcoidosis.

Fourteen patients with CNS manifestations of neurosarcoidosis were evaluated by MR imaging and CT. Evaluations were done on a 0.5-T superconductive magnet with T1- and T2-weighted sequences. CT with contrast was obtained in all patients. The granulomatous lesions were classified by location into basilar, convexity, intrahemispheric, and periventricular white-matter involvement. Hydrocephalus with or without an associated lesion was also noted. MR determined the presence of disease in all patients (100%), but was less accurate than CT in depicting disease in two patients (14%). CT determined the presence of disease in 12 patients (85%) and was less accurate than MR in delineating hypothalamic involvement in two patients and periventricular white-matter disease in three patients. There was great variability in the appearance of intracranial sarcoidosis on MR. Three patients had lesions that were isointense or hypointense (relative to cerebral cortex) on both T1- and T2-weighted images while nine patients had lesions that were hyperintense on T2-weighted images. Convexity involvement and hydrocephalus were well documented by both CT and MR. These results indicate that both MR and CT are helpful in fully evaluating a patient with suspected intracranial sarcoidosis.

Adult↗