4. Hrvatski kongres kliniËke citologije 4th Croatian Congress ... - Penta
4. Hrvatski kongres kliniËke citologije 4th Croatian Congress ... - Penta
4. Hrvatski kongres kliniËke citologije 4th Croatian Congress ... - Penta
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Cytotechnology - Oral Presentations<br />
NUMBER OF COUNTING CELLS AND CYTOSPINS SELECTION INFLUENCES ON<br />
BRONCHOALVEOLAR LAVAGE CELL PROFILES<br />
Harabajsa S, Martinčić J, Peharec I, Popek B, Šušković- Medved S, Zadražil B,<br />
Smojver-Ježek S<br />
University Hospital for Lung Diseases Jordanovac, Zagreb, Croatia<br />
BAL fluid cells count provides information about presence or absence of interstitial lung<br />
diseases. BAL fluid samples were taken from 50 patients hospitalized in University Hospital<br />
for Lung Diseases Jordanovac in Zagreb, Croatia. The samples of BAL fluid were<br />
prepared by cytocentrifuge. From each sample two cytospin were selected (C1 and C2)<br />
and after determing adequacy, counted up to 200 and 400 cells. After air-drying, samples<br />
were stained according to May Grünwald Giemsa (MGG). Cells were counted by<br />
light microscope at magnification of 400 x. Obtained results were analyzed in Statistics<br />
version 6 and Med Calc. Results for bronchial epithelial cells, alveolar macrophages,<br />
lymphocytes and neutrophilic granulocytes showed insignificant statistical differences<br />
between groups (p>0.05). Eosinophils percentages showed borderline insignificant statistical<br />
difference between groups of these cells (p=0.052). As it was exemplificated, the<br />
percentages of differentiated cells do not significant differ according to differentiation on<br />
200 and 400 cells and cytospin selection.<br />
suzana.harabajsa@zg.t-com.hr<br />
ERYTHROCYTE MORPHOLOGY IN MALIGNANT URINE SAMPLES<br />
Knežević G, Parigros K, Milas M, Šušterčić D, Kardum-Skelin I<br />
Merkur University Hospital, Zagreb, Croatia<br />
The aim of the study was to show the origin of erythrocytes in malignant urine sample,<br />
assuming that a finding of 80% and more of dysmorphic erythrocytes indicated the<br />
bleeding to derive from upper urinary tract, and 80% and more of smooth erythrocytes<br />
indicated them to derive from lower urine tract; in urine samples without significant<br />
origin of bleeding there were 20%-80% mixed results with both dysmorphic and isomorphic<br />
erythrocytes. Data were collected from the findings recorded in malignant urine<br />
samples received. Samples were fresh native urine sediment contrast stained with 0.1%<br />
Safranin solution and analyzed under light microscope (X40). Out of 72 patients with<br />
malignant cells detected in urine, the origin of erythrocytes was identified in 25 patients<br />
(nine female and 16 male) through 190 samples (approximately 4 samples per patient).<br />
A mixed origin of erythrocytes was identified in 70 (36.9%) samples, 55 (28.9%) samples<br />
did not have enough erythrocytes to define their origin, dysmorphic erythrocytes were<br />
found in 53 (27.9%) samples, and isomorphic erythrocytes in 12 (6.3%) samples. In conclusion,<br />
there was no specific connection between malignant cell findings in urine and<br />
origin of erythrocytes. However, the high presence of mixed erythrocyte origin in malignant<br />
samples may suggest that the existence of a malignant process and renal disease<br />
should be taken in consideration.<br />
gordana.knezevic1@zg.t-com.hr<br />
175<br />
4 th <strong>Croatian</strong> <strong>Congress</strong> of Clinical Cytology / 1 st <strong>Croatian</strong> Symposium of Analytical Cytology / 2 nd <strong>Croatian</strong> Symposium of Cytotechnology