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Bone marrow aspirate

Beckman Elutriation Method. The Beckman elutriation method uses a chamber designed so that the centrifugal effect of the radial inward fluid flow is constant (Fig. 3). The separation chambers are made of transparent epoxy resin which faciUtates observation of the movements of the cell boundary in strobe light illumination. This enables detection of the radius at which the cells are separating. When a mixture of cells, eg, mononuclear white cells, enters the chamber, separation can be achieved by fine tuning centrifuge speed and inward fluid flow to the specific cell group. This is a laboratory method suitable for relatively small numbers of cells. Chambers are available in sizes to handle 2-3 x 10 , 1 2 x 10 , and 1 x 10 ° cells. The Beckman chambers can be appHed to collect mononuclear cells from bone marrow aspirates. [Pg.522]

RH had a bone marrow aspiration performed on days 15 and 29 that showed morphologic remission. The MRD on day 29 was less than 0.1%. RH completed her induction therapy and started intensification therapy. [Pg.1404]

Bone marrow aspirates and biopsy specimen from HIV-positive patients with plasmacytosis (T3) were analyzed to identify the pathologic correlates of polyclonal and monoclonal hypergammaglobulinemia in these patients. Serum protein electrophoresis and immunoelectrophoresis revealed monoclonal spikes in 25% of patients tested 75% of patient tests showed polyclonal hypergammaglobulinemia. [Pg.217]

Phase I data were presented at the 95th AACR meeting, March 2004. Normal healthy male volunteers were subjected to bone marrow aspirations prior to and 4 h following a single 25 mg oral dose of the compound or placebo. L21649 achieved plasma concentrations of 103.4 nM at 4 h post-dose. In July 2004, similar clinical data were presented at the 29th National Medicinal Chemistry symposium. The PK/PD correlated well, and at that time, it was believed that the plasma levels should be closer to the EC90 levels for maximal efficacy. [Pg.367]

Monitor WBC count and differential daily. Consider bone marrow aspiration to ascertain granulopoietic status. If granulopoiesis is deficient, consider protective isolation. If infection develops, perform cultures and institute antibiotics. [Pg.1131]

Because of early dissemination, staging of patients with small-cell lung cancer is more extensive than for patients with NSCLC. It is important to rule out distant metastasis because it will change the role of thoracic radiation in the treatment of these patients. Staging should include a complete history and physical examination, CAT scans of chest and upper abdomen to include the liver and adrenal glands, brain MRI scan, bone scan, complete blood count, and a possible bone marrow aspiration and biopsy. [Pg.198]

Newer strategies for stem cell identification have been developed based on the knowledge of cell functions. A primitive and multipotential subpopulation of bone marrow mononuclear cells has been identified on the basis of the intracellular presence of aldehyde dehydrogenase (ALDH). Those cells can be marked on the basis of the presence of ALDH and are called aldehyde dehydrogenase-bright cells (ALDH cells), allowing for their separation from a bone marrow aspiration mononuclear subpopulation under fluorescence-activated cell sorter (FACS) analysis. [Pg.95]

Midazolam 0.2 mg/kg Used as a single dose prior to lumbar puncture or bone marrow aspiration Friedman et ah, 1991... [Pg.635]

Friedman, A.G., Mulhern, R.K., Fairclough, D., et al. (1991) Midazolam premedication for pediatric bone marrow aspiration and lumbar puncture. Med Pediatr Oncol 19 499-504. [Pg.640]

If WBC count is less than 2,000/mm or ANC is less than 1,000/mm , discontinue clozapine and do not rechallenge. Perform WBC and differential counts daily until WBC count is greater than 3,000/mm and ANC is greater than 1,500/mm. Then monitor twice weekly until WBC count returns to more than 3,500/mm and ANC is greater than 2,000/mm . Then monitor weekly for 4 weeks. Treat any infection with antibiotics. Consider bone marrow aspiration to ascertain granulopoietic status. If granulopoiesis is deficient, consider protective isolation. [Pg.112]

Nevertheless, immunotoxins may be useful for purging cancer cells in bone marrow aspirate isolated from patients undergoing autologous bone marrow transplantation [29,30]. When no suitable bone marrow donor is available, the patients own marrow cells are collected for repopulation of immune cells after radiation and chemotherapy. The small fraction of leukemic cells in autologous bone marrow cells can be removed with immunotoxins before they are reintroduced to the patient for restoring their immune system. Because this procedure... [Pg.284]

Adhesion of mononuclear cells from human bone marrow aspirates (BM-MNC) to tissue culture plastic and removal of nonadherent cells during the first days of culture selects for a population of proliferating spindle-shaped fibroblast-like non-... [Pg.100]

The versatility of immunophenotypic analysis has enhanced its usefulness. Immunophenotyping can be performed on a variety of specimens including cryop-reserved tissue sections, routinely preserved tissue sections, cells in suspension, tissue-touch preparations ( touch preps ), fine-needle aspiration smears, cytology thin preps and smears, as well as bone marrow aspirate smears. With the evolution of medical science and technical ability the number and types of antigens that can be detected in each type of preparation have greatly increased. Furthermore, as an additional result of these technical and scientific advances, immunophenotyping, particularly of routinely fixed tissue sections, can be performed reliably in many laboratories. [Pg.294]

Cells in suspension, i.e., bone marrow aspirates, peripheral blood, effusions, etc. [Pg.303]

An individualized approach toward treatment only of patients whose blasts are sensitive to I-ASP seems to be reasonable but is difficult to perform espe-risHv if their numbers are low and inaccessible for biochemical studies. As a feasible alternative, the expression of Laspaiagine synthetase mRNA should be monitored in bone marrow aspirates and correlated to the overall treatment... [Pg.249]

In addition to the cellular expression on malignant blast cells in AML, elevated levels of suPAR were found in plasma from leukemia patients [18]. In a longitudinal study, in which patients receiving chemotherapy were monitored, it was demonstrated that the suPAR level in plasma from patients with AML correlated with the number of circulating tumor cells and that these were reduced after chemotherapy. In plasma from AML patients, suPAR(II III) was detected in addition to intact suPAR. This is in contrast to findings in plasma from healthy individuals and from the ovarian cancer patients described above [144]. suPAR(II III) was also present in plasma made from bone marrow aspirates. The other cleaved form, uPAR(I), was only identified in urine. Lysates of the leukemic cells contained both intact uPAR and uPAR(II-III). The amounts of suPAR(II III) in plasma and uPAR(I) in urine were decreased following chemotherapy. In healthy controls, intact uPAR was detected in lysates from mononuclear cells in blood and suPAR(I-III) in plasma and bone marrow aspirates, while suPAR(II-III) was detected in urine [18]. [Pg.90]

A 6-month-old child was breast-fed exclusively by a mother who had been a strict vegetarian for at least 7 years. He was totally unresponsive to stimuli. His hemoglobin was 5.7 g/dL, and his bone marrow aspirates showed megaloblastic changes in blood cells. His serum folate and iron were normal. His urine contained increased amounts of homocystine, methylmalonic acid, and glycine. Propose a reason for this infant s illness, and discuss its biochemical etiology. Discuss other possible reasons for the same or similar symptoms in a patient. Explain the abnormal serum and urine chemistries. [Pg.151]

Contraindications. It is illogical to give iron in the anaemia of chronic infection where utilisation of iron stores is impaired but such patients may also have true iron deficiency. This may be difficult to diagnose without direct visualisation of stores in a bone marrow aspirate. Iron should not be given in haemolytic anaemias unless there is also haemo-globinuria, for the iron from the lysed cells remains in the body. Moreover the increased erythropoiesis associated with chronic haemolytic states stimulates increased iron absorption and adding to the iron load may cause haemosiderosis. [Pg.589]

The pathogenesis of bone marrow aplasia after chloramphenicol is still uncertain. Compared with normal cells, bone marrow aspirates from patients with bone marrow aplasia are relatively resistant to the toxic effects of chloramphenicol in vitro. This has been... [Pg.708]

X 10 / , with 40% eosinophils on bone marrow aspiration and a markedly high IgE concentration. Radiological examination showed diffuse jejunal and ileal wall thickening and gross ascites with numerous eosinophils. Complete resolution was obtained after interferon alfa withdrawal and prednisolone treatment. There was no recurrence after prednisolone was withdrawn. [Pg.1807]


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See also in sourсe #XX -- [ Pg.309 , Pg.313 , Pg.323 , Pg.325 ]




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