Kalliopi Kyrkou
National and Kapodistrian University of Athens
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Acta Cytologica | 1998
Michael J. O’Brien; Masayoshi Takahashi; Gérard Brugal; Heinz Christen; Thomas Gahm; Roberta M. Goodell; Peter Karakitsos; Ernest A. Knesel; Terry Paul Kobler; Kalliopi Kyrkou; Sylvain Labbe; Elizabeth L. Long; Laurie J. Mango; Euphemia McGoogan; Martin Oberholzer; Albrecht Reith; Christoph Winkler
ISSUES Optical digital imaging and its related technologies have applications in cytopathology that encompass training and education, image analysis, diagnosis, report documentation and archiving, and telecommunications. Telecytology involves the use of telecommunications to transmit cytology images for the purposes of diagnosis, consultation or education. This working paper provides a mainly informational overview of optical digital imaging and summarizes current technologic resources and applications and some of the ethical and legal implications of the use of these new technologies in cytopathology. CONSENSUS POSITION Computer hardware standards for optical digital imagery will continue to be driven mainly by commercial interests and nonmedical imperatives, but professional organizations can play a valuable role in developing recommendations or standards for digital image sampling, documentation, archiving, authenticity safeguards and teleconsultation protocols; in addressing patient confidentiality and ethical, legal and informed consent issues; and in providing support for quality assurance and standardization of digital image-based testing. There is some evidence that high levels of accuracy for telepathology diagnosis can be achieved using existing dynamic systems, which may also be applicable to telecytology consultation. Static systems for both telepathology and telecytology, which have the advantage of considerably lower cost, appear to have lower levels of accuracy. Laboratories that maintain digital image databases should adopt practices and protocols that ensure patient confidentiality. Individuals participating in telecommunication of digital images for diagnosis should be properly qualified, meet licensing requirements and use procedures that protect patient confidentiality. Such individuals should be cognizant of the limitations of the technology and employ quality assurance practices that ensure the validity and accuracy of each consultation. Even in an informal teleconsultation setting one should define the extent of participation and be mindful of potential malpractice liability. ONGOING ISSUES Digital imagery applications will continue to present new opportunities and challenges. Position papers such as this are directed toward assisting the profession to stay informed and in control of these applications in the laboratory. Telecytology is an area in particular need of studies of good quality to provide data on factors affecting accuracy. New technologic approaches to addressing the issue of selective sampling in static image consultation are needed. The use of artificial intelligence software as an adjunct to enhance the accuracy and reproducibility of cytologic diagnosis of digital images in routine and consultation settings deserves to be pursued. Other telecytology-related issues that require clarification and the adoption of workable guidelines include interstate licensure and protocols to define malpractice liability.
Acta Cytologica | 1997
Anna Ioakim-Liossi; Petros Karakitsos; Kyriaki Aroni; Kalliopi Delivelioti; Vassiliki Fotiou; Stelios Fotiou; Kalliopi Kyrkou
OBJECTIVE To investigate p53 protein expression and DNA content in imprints from surgical biopsies of common epithelial tumors of the ovary. STUDY DESIGN The study was based on 60 cases of epithelial tumors of the ovary (15 benign, 3 border-line and 42 malignant). For the demonstration of p53 protein, immunocytochemical staining with the avidin-extravidin technique was performed using monoclonal antibody p53 DO-7. DNA content was measured by image cytometry after Feulgen staining. RESULTS There was a strong correlation between p53 expression and aneuploidy, with the difference between diploid and aneuploid tumors statistically significant (P < .001). A correlation was found between DNA ploidy, histologic grade and clinical stage (P < .001 and P < .05), respectively. There was no correlation between DNA ploidy and histologic type (P = .89). No correlation was observed between p53 protein expression and grade or clinical stage of the tumors. Nevertheless, a correlation of p53 expression between early (I, II) and advanced stages (III, IV) (P < .05) was observed. All benign and borderline tumors were diploid and did not express p53 protein. CONCLUSION The results of the present study and the data in the literature stress the value of p53 expression and DNA ploidy in assessing the malignant potential of common epithelial ovarian cancers. However, the clinical application of these data requires further study.
Acta Cytologica | 1997
Anna Ioakim-Liossi; Petros Karakitsos; Christos Markopoulos; Kyriaki Aroni; Kalliopi Delivelioti; John Gogas; Kalliopi Kyrkou
OBJECTIVE To investigate pS2 protein expression and estrogen (ER) and progesterone receptor (PR) status of imprints from surgical biopsies of breast cancer cases in relation to the histologic grade of malignancy. STUDY DESIGN The study group consisted of 50 cases of primary breast carcinomas. For the demonstration of pS2 protein expression an immunocyto-chemical avidin-biotin complex technique was applied. Monoclonal antibody pS2 was used as the primary antibody, diaminobenzidine as the chromogene and hematoxylin as the counterstain. For the evaluation of ERs and PRs, a biochemical method was applied. RESULTS Sixty-two percent of breast cancer cases showed positive expression of pS2. Of the 31 pS2+ cases, 74% had positive ERs and PRs. A statistically significant difference was observed between pS2 protein expression, ER+, PR+ and histologic grade of malignancy (P < .001). CONCLUSION Two groups of breast cancer cases can be distinguished: one group that is ER+, PR+ and pS2+, with low malignancy potential, and another group that is ER-, PR- and pS2-, with high malignancy potential.
Cytopathology | 1992
Pauline Athanassiadou; Kalliopi Kyrkou; L. G. Antoniades; Peter Athanassiades
The influence of Tamoxifen on the vaginal epithelium of 33 premenopausal and 99 post‐menopausal women with primary advanced breast cancer was investigated. the karyopyknotic index (KPI) values were assessed before starting therapy and at monthly intervals during therapy with Tamoxifen. A decrease in the KPI in menstruating women and a slight but definite increase in KPI values in post‐menopausal women were observed.
Cytopathology | 1997
S. Veneti; Pauline Athanassiadou; C. Kandaraki; Kalliopi Kyrkou
In order to appraise the usefulness of HMFG2 and thyroglobulin (Tg) as specific markers for the diagnosis of thyroid disease, we studied 63 FNA smears. Cases tested included 30 benign (nine colloid goitres, six cases of Hashimotos thyroiditis, six Hürthle cell adenomas, nine follicular adenomas) and 33 malignant lesions (nine follicular carcinomas, 12 papillary carcinomas, nine anaplastic carcinomas, three medullary carcinomas). All cases with malignant lesions except the anaplastic carcinomas were positive for HMFG2. Immunoreactive cells to HMFG2 were also found in 15 adenomas out of 30 benign cases. Positive Tg reaction was found in benign and malignant thyroid lesions, except six cases of Hashimotos thyroiditis, nine anaplastic and three medullary carcinomas. The results obtained indicate that morphology paired with immunocytochemistry can usually depict a more specific profile of thyroid lesions for better evaluation of the pathology.
Acta Cytologica | 1994
Pauline Athanassiadou; Peter Athanassiades; D. Lazaris; Kalliopi Kyrkou; Efthalia Petrakakou; D. Aravantinos
Acta Cytologica | 1995
Pauline Athanassiadou; Psyhoyou H; Kalliopi Kyrkou; Peter Athanassiades; Moulopoulos S
Diagnostic Cytopathology | 1995
Pauline Athanassiadou; Peter Athanassiades; Charalambos Kostopoulos; Kalliopi Kyrkou; Efthalia Petrakakou; Sofia Veroni
Diagnostic Cytopathology | 1987
G. N. Antonakopoulos; E. Lambrinaki; Kalliopi Kyrkou
Cytopathology | 1998
Petros Karakitsos; E. M. Botsoli-Stergiou; Anne Ioakim-Liossi; Georgoulakis J; Christos Markopoulos; John Gogas; Kalliopi Kyrkou