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1.
AJNR Am J Neuroradiol ; 19(1): 151-6, 1998 Jan.
Article in English | MEDLINE | ID: mdl-9432173

ABSTRACT

PURPOSE: We compared visibility of residual juvenile cerebellar pilocytic astrocytomas (JPAs) on early postoperative and follow-up MR studies to determine whether early postoperative MR imaging has a valid role as a baseline study. METHODS: We reviewed the MR images of 21 consecutive children who had undergone resection of cerebellar JPA. The diagnosis of residual tumor was made on the basis of nodular enhancement that corresponded to enhancing tumor on the preoperative MR studies and/or nonenhancing nodular T2 signal that corresponded to nonenhancing tumor. Because no patient received chemotherapy or radiation therapy, abnormal T2 signal or enhancement on the early postoperative study that resolved on the follow-up study was presumed to be due to peritumoral edema and/or surgical manipulation. Nodular T2 signal and/or enhancement in the tumor bed not seen on the initial postoperative MR study but present on the subsequent MR study and unchanged on serial follow-up MR studies was presumed to represent residual tumor rather than tumor that had recurred. RESULTS: Compared with follow-up studies, the initial postoperative MR images were true-positive for residual tumor in six patients, false-positive in five, equivocal for residual tumor in four, true-negative in five, and false-negative in one. Residual tumor did not consistently enhance, and peritumoral edema and changes resulting from surgical manipulation tended to mask or simulate residual tumor. CONCLUSION: Early postoperative MR imaging is not accurate in differentiating residual JPA from postoperative changes, and the role of early postoperative MR imaging as a baseline study for comparison with further studies is questionable.


Subject(s)
Astrocytoma/diagnosis , Astrocytoma/surgery , Cerebellar Neoplasms/diagnosis , Cerebellar Neoplasms/surgery , Magnetic Resonance Imaging , Neoplasm, Residual/diagnosis , Adolescent , Child , Child, Preschool , Diagnosis, Differential , False Negative Reactions , False Positive Reactions , Female , Follow-Up Studies , Humans , Infant , Male , Postoperative Period
2.
Pediatr Neurosurg ; 22(1): 8-14, 1995.
Article in English | MEDLINE | ID: mdl-7888393

ABSTRACT

Despite its usefulness in adults with cerebral gliomas, indications for thallium-201 single-photon emission computed tomography (SPECT) in pediatric brain tumor patients are not well defined. We prospectively compared thallium SPECT with gadolinium-enhanced MR (Gd-MR) to determine if thallium SPECT provides clinically useful information that cannot be derived from Gd-MR. We studied 24 pediatric brain tumor patients, 7 at presentation and 17 during therapy. MR imaging included T2 and pre- and postgadolinium T1 images. Thallium SPECT was done within 48 h of MR imaging; thallium indices were calculated for 12 of 14 lesions which showed thallium uptake. Surgery and/or clinical follow-up are available in all patients. The tumors included pilocytic astrocytoma (7), medulloblastoma (5), brainstem glioma or glioblastoma (4), germinoma (3), optic glioma (2), mixed glioma (1), primitive neuroectodermal tumor (1), and choroid plexus carcinoma (1). Among the primary tumors, compared to MR, thallium SPECT was false-negative for tumor in 1 patient and true-positive in 6 patients. Among the patients studied while on therapy, compared to MR, thallium SPECT was true-negative for tumor in 7, true-positive in 5, false-negative in 3, and false-positive in 2. In both groups of patients, thallium SPECT underestimated tumor burden as nonenhancing regions of the tumors were not thallium-avid. Thallium indices did not correlate with histologic grade, biologic aggressiveness, or tumor type. We were unable to establish indications for the use of thallium SPECT in this setting as there was little clinically useful information derived from thallium SPECT that was not provided by Gd-MR.


Subject(s)
Brain Neoplasms/diagnosis , Contrast Media , Glioma/diagnosis , Magnetic Resonance Imaging/methods , Organometallic Compounds , Pentetic Acid/analogs & derivatives , Thallium Radioisotopes , Tomography, Emission-Computed, Single-Photon/methods , Adolescent , Brain/pathology , Brain Neoplasms/pathology , Brain Neoplasms/surgery , Child , Female , Gadolinium DTPA , Glioma/pathology , Glioma/surgery , Humans , Infant , Male , Neoplasm Recurrence, Local/diagnosis , Neoplasm Staging , Postoperative Complications/diagnosis , Prognosis
3.
Peptides ; 5(2): 429-33, 1984.
Article in English | MEDLINE | ID: mdl-6473166

ABSTRACT

Immunoreactive vasoactive intestinal peptide (VIP) was measured in lumbar and ventricular cerebrospinal fluid (CSF) from patients with various neurological disorders and in 2 hour aliquots of cisternal fluid removed continuously from rhesus monkeys. Although most of the VIP in concentrated pools of human ventricular fluid and of monkey cisternal fluid co-eluted with synthetic porcine VIP28 on a column of Sephadex G-25 superfine, there was evidence that smaller immunoreactive fragments were also present. A circadian pattern of CSF VIP concentration was observed in 2 of the 3 monkeys studied, with highest levels occurring at night and lowest during the day. Ventricular fluid VIP levels were highest in hydrocephalic children and lowest in patients with multiple sclerosis or epilepsy, while VIP was not detectable in ventricular fluid from patients in coma following a severe head injury. There were no significant differences in VIP concentrations in CSF from patients with dystonia. Parkinson's disease, or Alzheimer's disease, suggesting that VIP containing neurons are not affected in these disorders. Lumbar fluid VIP levels were low in patients undergoing aneurysm surgery. Since VIP is a potent vasodilator, these findings may have important implications in relation to the development of vasospasm following subarachnoid hemorrhage.


Subject(s)
Nervous System Diseases/cerebrospinal fluid , Vasoactive Intestinal Peptide/cerebrospinal fluid , Chromatography, Gel , Drug Stability , Humans , Organ Specificity , Radioimmunoassay
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