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<metadata xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dc="http://purl.org/dc/elements/1.1/"><dc:title>Cellularity of routinely prepared cell blocks</dc:title><dc:creator>Srebotnik-Kirbiš,	Irena	(Avtor)
	</dc:creator><dc:creator>Strojan Fležar,	Margareta	(Avtor)
	</dc:creator><dc:subject>cell block</dc:subject><dc:subject>cellularity</dc:subject><dc:subject>cytology</dc:subject><dc:subject>preparation of method</dc:subject><dc:description>Objective: Formalin-fixed, paraffin-embedded (FFPE) cell blocks (CBs) are widely used for processing cytology specimens, but preparation methods remain variable and non-standardised. Low cellularity is a common limitation that may compromise diagnostic utility. This study aimed to evaluate the cellularity of routinely prepared CBs across different preparation methods, laboratories and sample types. 
Methods: Each laboratory in this multicentre observational study retrospectively assessed 50 consecutive CBs prepared using a single method. Cellularity of Haematoxylin and Eosin (H&amp;E)-stained sections was semi-quantitatively evaluated by two independent reviewers per laboratory in four categories: acellular, low (≤ 100 cells), medium (100-500 cells) and high cellular (&gt; 500 cells). The proportion of poorly cellular CBs (acellular + low cellular) was compared across methods, laboratories and sample types using non-parametric tests. 
Results: Cellularity was assessed for 1817 CBs prepared using Agar (22%), HistoGel (19%), Plasma-Thrombin (19%), Cellient (17%), In-house (15%) and Shandon/Epredia (8%) methods. The proportion of poorly cellular CBs ranged from 4% to 80% across laboratories (mean 27%, median 25%), with no consistent clustering by method. Median proportions by method ranged from 12% (Cellient) to 35% (Agar), but inter-method differences were not statistically significant (p &gt; 0.05). Substantial variability was observed both across and within sample types and preparation methods. 
Conclusions: The study revealed marked variability in the proportion of poorly cellular CBs among preparation methods and laboratories, highlighting the need for improved processing and monitoring of CB adequacy.</dc:description><dc:date>2026</dc:date><dc:date>2026-07-17 08:15:48</dc:date><dc:type>Članek v reviji</dc:type><dc:identifier>184919</dc:identifier><dc:identifier>UDK: 616:576</dc:identifier><dc:identifier>ISSN pri članku: 0956-5507</dc:identifier><dc:identifier>DOI: 10.1111/cyt.70065</dc:identifier><dc:identifier>COBISS_ID: 271666691</dc:identifier><dc:language>sl</dc:language></metadata>
