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1.
J Comput Assist Tomogr ; 7(1): 175-6, 1983 Feb.
Article in English | MEDLINE | ID: mdl-6826847

ABSTRACT

For enhanced computed tomography, rapid injections through small bore needles can be easily accomplished utilizing an infusion pump. A reduction in radiation exposure to medical personnel is an associated benefit.


Subject(s)
Contrast Media/administration & dosage , Infusions, Parenteral/instrumentation , Tomography, X-Ray Computed/instrumentation , Adolescent , Child , Humans , Tomography, X-Ray Computed/methods
2.
Med Pediatr Oncol ; 9(2): 133-41, 1981.
Article in English | MEDLINE | ID: mdl-6939956

ABSTRACT

From 1972-1974, 228 children began treatment for acute lymphocytic leukemia and were prospectively assessed for neurologic complications. After CNS irradiation (2,400 rad) and intrathecal methotrexate (MTX), they received weekly intravenous maintenance therapy with MTX alone (40-60 mg/m2; 20 patients) or MTX (10-30 mg/m2) with other drugs (208 patients). Signs of leukoencephalopathy appeared in 11 children (nine without CNS leukemia) after 4-15 months of IV MTX alone, and included lethargy, seizures, spasticity, paresis, drooling, and dementia. Before or during the clinical onset, EEG frequencies slowed (all ten patients tested). Radionuclide scans showed periventricular accumulation of 99mTc (9/11 patients) and remained abnormal for greater than or equal to six months in eight patients. Cranial computed tomograms or neuropathology findings (five patients each) demonstrated leukoencephalopathy (nine patients) and radiation-related microangiopathy (ten patients). Severe neurologic and neuropsychologic dysfunctions were present in four long-term survivors.


Subject(s)
Leukemia, Lymphoid/drug therapy , Methotrexate/adverse effects , Substance-Related Disorders/etiology , Brain/pathology , Child , Child, Preschool , Electroencephalography , Female , Humans , Infant , Male , Methotrexate/therapeutic use , Substance-Related Disorders/diagnosis , Substance-Related Disorders/pathology
3.
J Pediatr Surg ; 13(3): 281-5, 1978 Jun.
Article in English | MEDLINE | ID: mdl-209165

ABSTRACT

Nodular renal blastema and nephroblastomatosis were present in 8 of 118 patients (6.8%) with Wilms' tumor. Five of these 8 patients (63%) had bilateral Wilms' tumors. Two had hemihypertrophy. Preoperative renal angiograms were accurate in detecting these metanephric anomalies. The surgical approach consisted of removal of the most diseased kidney and biopsy for diffuse tumors and wedge resections for localized tumors for the remaining kidney. Postoperatively, radiation was administered when tumor extended outside the kidney. Chemotherapy consisted of vincristine and dactinomycin for 18 mo and adriamycin for 6 mo. This method of management resulted in tumor-free survival of these 8 patients for 1--44 mo (median 24 mo). Nodular renal blastema and nephroblastomatosis may possibly develop into Wilms' tumor. All of these three conditions respond to surgery, chemotherapy, and radiation. When a Wilms' tumor is encountered, it is better to explore and possibly biopsy the opposite kidney. There is a place for second-look laparotomy in this spectrum of congenital anomalies.


Subject(s)
Kidney Neoplasms/complications , Wilms Tumor/complications , Child , Child, Preschool , Female , Humans , Infant , Kidney/pathology , Kidney Neoplasms/pathology , Kidney Neoplasms/surgery , Kidney Neoplasms/therapy , Male , Wilms Tumor/pathology , Wilms Tumor/surgery , Wilms Tumor/therapy
4.
Hum Pathol ; 9(2): 199-209, 1978 Mar.
Article in English | MEDLINE | ID: mdl-205499

ABSTRACT

The ultrastructural features of a malignant histiocytoma of the acromial process of the scapula were studied. Material was obtained from two surgical biopsy specimens and an amputation specimen from the tumor. Cells possessing characteristics of histiocytes, fibroblasts, xanthoma cells, and multinucleated giant cells were present throughout the tumor. Smaller numbers of undifferentiated cells and lymphocytes were also observed. Intimate cytoplasmic interdigitations between adjacent tumor cells were found, and instances of degenerating intracytoplasmic cells, possibly representing phagocytosis, were observed. Specimens stained with periodic acid-Schiff reagent with and without exposure to diastase, examined by light microscopy, showed that numerous cells contained phagocytized material consisting of degenerating cells rather than cytoplasmic glycogen. Intraumor lymphocytes apparently represented an inflammatory reaction to the tumor. The tumor giant cells and xanthoma cells were probably modified histiocytes. Results of the study were compared with previous reports of ultrastructural studies of malignant histiocytoma of soft tissues. Fundamental similarities between such studies and this one suggested that the progenitor cell is a histiocyte, whether arising in bone or in soft tissues, and that the progenitor cell is capable of differentiation in both histiocytic and fibroblastic directions.


Subject(s)
Acromion , Bone Neoplasms/ultrastructure , Histiocytoma, Benign Fibrous/ultrastructure , Scapula , Adolescent , Bone Neoplasms/pathology , Fibroblasts/ultrastructure , Histiocytes/ultrastructure , Histiocytoma, Benign Fibrous/pathology , Humans , Lymphocytes/ultrastructure , Male
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