Pregled bibliografske jedinice broj: 909653
Screening difficulties in detection of Pneumocystis (carinii) jiroveci
Screening difficulties in detection of Pneumocystis (carinii) jiroveci // Journal of Cytopathology, 23 (Suppl. 1), 81-144 / Herbert, A ; Cochand-Priollet, B (ur.).
Cavtat, Hrvatska: Wiley-Blackwell, 2012. str. 96-96 (poster, međunarodna recenzija, sažetak, stručni)
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Naslov
Screening difficulties in detection of Pneumocystis (carinii) jiroveci
Autori
Harabajsa, Suzana ; Popek, Božena ; Šušković- Medved, Snježana ; Zadražil, Barica ; Juroš, Zrinka ; Vrabec Branica, Božica ; Smojver- Ježek, Silvana
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, stručni
Izvornik
Journal of Cytopathology, 23 (Suppl. 1), 81-144
/ Herbert, A ; Cochand-Priollet, B - : Wiley-Blackwell, 2012, 96-96
Skup
37th European Congress of Cytology
Mjesto i datum
Cavtat, Hrvatska, 30.09.2012. - 03.10.2012
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
Screening ; Pneumocystis (carinii) jiroveci ; cytology
Sažetak
Introduction: Pneumocystis (carinii) jiroveci (PC) is a frequent cause of pneumonia in immunocompromised patients. Aim of the study: To analyse difficulties of PC detection in routinely obtained bronchoscopic samples. Material and methods: In the study were included 284 patients with clinical suspected PC pneumonia and bronchoscopic examination. Each sample of non - filtered bronchoalveolar lavage fluid (BAL) and bronchoscopic aspirate was centrifuged and stained with MGG, Kwik Diff and Rapid Papa. Slides were analysed by light microscope under magnification 400 and 1000 x. Trophozoites and cyst stage aggregations of PC were searched. Results: During five year observation period 284 samples were analysed. The results numbered 241 (84, 86%) BAL and 43 (15, 14%) bronchoscopic aspirates. PC forms were revealed in cytology slides of 11 (3, 87%) BAL samples. MGG stained trophozoites were presented as red dot like inclusions surrounded by pale blue cytoplasm. Kwik Diff more clearly represented trophozoites over standard MGG method. Rapid Papa represented clusters of PC cysts embedded in the foamy exudates providing honeycomb appearance. MGG, Kwik Diff and Rapid Papa didn’t stain cyst walls. Conclusion: BAL is a sample of choice for PC detection providing content of lower respiratory tract. Non adequate BAL containing erythrocytes, detritus and bacteria may cause screening difficulties. Background staining may also interfere with clarity and complicate screening. Clusters of stained mucus may look like PC clusters. Tumour cells, various fungal and viral infection cell changes may be found with PC and mislead interpretation.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
POVEZANOST RADA
Ustanove:
Klinički bolnički centar Zagreb
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE