No abstract available.
Fixatives* ; Mast Cells*

Migration of the fixation device to a part of the body is well known complication of fracture treatment. However, few reports of this complication have appeared in the literature. The present report concerns two instances of the migration of a K-wire and a Steinmann pin from the acromioclavicular joint, respectively, into the neck. It appears that if wires and pins are used for fixation, the lateral ends should be bent to prevent medial migration, and as soon as the desired therapeutic results have been obtained, these must be subsequently removed.
Acromioclavicular Joint ; Fixatives ; Neck

PURPOSE: To prepare the appropriate guideline in choosing the internal fixatives for the intertrochanteric fractures of the femur in the elderly. MATERIALS AND METHODS: We reviewed 95 cases of intertrochanteric fractures of the femur from January, 1999 to December, 2003. We fixed the fracture with Proximal Femoral Nail in 37 cases (PFN group), Dynamic Hip Screw in 56 (DHS group), Dynamic Condylar Screw in 2 cases (DHS group). We reviewed operation time, blood loss during operation, changes in neck-shaft angle and sliding of lag screw. RESULTS: There were no significant differences in the parameters between the 2 groups in stable fracture. In unstable fractures, operation time in PFN group and DHS group revealed 103.9 and 128.2 minutes respectively; mean amount of blood loss during operation revealed 523.2 and 573.1 ml respectively. Mean changes in the neck-shaft angle at final follow-up in PFN group and DHS group revealed 4.6 degrees and 4.1 degrees; sliding of lag screw averaged 3.4 and 6.5 mm respectively. Among the DHS group, cases of additional fixation with trochanteric supporting plate revealed 3.1 degrees of changes in neck-shaft angle and 4.2 mm of lag screw sliding. CONCLUSION: In cases of stable fractures, any fixative might suffice. In cases of unstable fractures, there were no significant differences in results of treatment between these two groups, however, PFN group revealed shoter operation time and less blood loss during operation. It seemed to be necessary to apply additional fixation with trochanteric supporting plate when using DHS in unstable cases.
Aged* ; Femur* ; Fixatives* ; Follow-Up Studies ; Hip ; Hip Fractures* ; Humans

The changes in the size of human oviduct and ovary after immersion in formalin (4%, 10%) were investigated. The results were as follows : 1. After fixation, the length of oviduct was significantly reduced to 93%, but the cross sectional area of oviduct was significantly increased. The length of oviduct showed no significant difference between 4% and 10% formalin. The length of ovarian ligament was also significantly reduced to 84% after fixation. 2. After fixation, the volume of oviduct was increased significantly and showed a difference between the two fixatives. The volume of oviduct in 4% formalin has increased to 107%, as compared to 103% increase in 10% formalin. 3. After fixation, the volume of ovary was increased significantly and showed a difference between the two fixatives. The volume of ovary in 4% formalin has increased to 109%, as compared to 103% increase in 10% formalin.
Animals ; Female ; Fixatives ; Formaldehyde* ; Humans* ; Immersion* ; Ligaments ; Ovary* ; Oviducts*

PURPOSE: With the development of MR Imaging techniques, MRI and MR spectroseopy can be used to evaluatespecimens both in vivo and in vitro. For extracted tissue specimens we wished to obtain MR images which correlatedwell with images obtained in vive; the purpose of this study was to determine which fixatives and time intervalbest facilitated this objective. MATERIALS AND METHODS: After in vivo MR imaging, sample tissues of liver, renalcortex and renal medulla were obtained from ten healthy rabbits. Each tissue sample was placed in 75% ethanol, 10%formalin, and 0.9% normal saline and MR scans of each sample were performed at 30 minutes, 11/2, 3, 6, and 12hours after resection. Signal intensities of the images were measured and their sequential changes were evaluated. RESULTS: On T1WI, signal intensities of both tissue specimens fixed in formalin and ethanol and untreatedspecimens increased significantly during the first 30 minutes. The increased signal intensity then seen for 12hours was greater than on T2WI. On T2WI, signal ntensities of tissue specimens fixed in formalin and ethanol anduntreated specimens showed no significant changes within the first 30 minutes; after that, they showed less signalintensity change for 12 hours than on T1WI. CONCLUSION: To obtain MR images with the same signal intensities as invivo tissue, MRI of tissue specimens in the untreated state should be performed as soon as possible afterresection. On T2WI, signal intensities of tissue specimens were more similar to in vivo tissue than on T1WI.
Ethanol ; Fixatives* ; Formaldehyde ; Liver ; Magnetic Resonance Imaging* ; Rabbits

Aluminum ; Fixatives ; Formaldehyde ; Humans ; Polymers ; Tissue Fixation ; instrumentation ; methods

Disinfectants ; Fixatives ; toxicity ; Formaldehyde ; toxicity ; Paraffin Embedding ; Tissue Fixation

Evaluation of serous effusions can include immunocytochemical stains that differentiate reactive mesothelial cell from adenocarcinoma cell. Among several positive mesothelial cell markers, we used desmin, CK5/6, WT1 and calretinin all known to have high sensitivity and specificity as selective mesothelial cell markers. We studied smears obtained with cytospin from 15 malignant and eight benign effusions. The mesothelial cells were positively stained by desmin, CK5/6, WT1 and calretinin in 60.9%, 29.1%, 26.7% and 56.5%, respectively among 8 benign and 15 malignant effusions; the adenocarcinoma cells were positively stained 6.7%, 13.3%, 1.0% and 0.0%, respectively among 15 malignant effusions. The percentage of positively stained mesothelial cells were somewhat lower for all antibodies compared to the results of previous studies. This was likely due to the differences in preparation methods and fixatives among studies. In conclusion, the use of desmin and calretinin were more valuable than CK5/6 and WT1 for distinguishing between reactive mesothelial cell and adenocarcinoma cells in serous effusion; however, choice of the proper preparation methods and fixatives are also important
Adenocarcinoma* ; Antibodies ; Calbindin 2 ; Coloring Agents ; Desmin ; Fixatives ; Sensitivity and Specificity

Antigens ; chemistry ; Fixatives ; chemistry ; Humans ; Hydrogen-Ion Concentration ; Immunohistochemistry ; methods ; Microwaves ; Staining and Labeling ; methods

BACKGROUND: Fixation of cells is a critical procedure that can determine the success of immunocytochemical staining (ICC) of cytospin slides. In this study, we evaluated the efficacy of a number of fixatives to determine the ideal fixative for ICC of cytospin slides. METHODS: Sixteen patients with metastatic neoplasm in the body cavity were enrolled. Cytospin slides were prepared from each patient using 5 different fixatives (cold acetone, 95% ethanol, 1:1 methanol:ethanol, 3.7% formalin, and 3:1 methanol:acetone), and the suitability of each for use with Wright's stain was compared. For 4 of the samples, appropriate ICCs were performed using all 5 fixatives and the results were compared, while for 11 samples, only the first 3 fixatives were used for ICC. RESULTS: Using Wright stain, cold acetone, 95% ethanol, and 1:1 methanol:ethanol fixatives all showed similar efficacy when compared to the conventional methanol fixation method. However, the stain quality using 3.7% formalin or 3:1 methanol:acetone fixatives was poor due to deterioration of cell adhesion and distortion of cell morphology. Using ICC, cold acetone fixative showed stronger and more tumor-specific stainability than the 95% ethanol (decreased stainability in 6 stained slides, false positive staining of histiocytes/neutrophils in 4 stained slides, no staining of CD3 and terminal deoxynucleotidyl transferase [TdT]) and 1:1 methanol:ethanol fixatives (decreased stainability in 3 stained slides, false positive staining of histiocytes/neutrophils in 2 stained slides, no staining of CD3 and TdT). CONCLUSIONS: Cold acetone fixative was the most efficacious among the 5 fixatives tested in this study; therefore, it is the most appropriate fixative in the preparation of cytospin slides for ICC.
Acetone ; Cell Adhesion ; Cold Temperature ; DNA Nucleotidylexotransferase ; Ethanol ; Fixatives ; Formaldehyde ; Humans ; Immunohistochemistry ; Methanol