role of the cell block in fine needle aspiration. acta cytol 1984;28: 630- 631.
Answers
Cell blocks prepared from residual tissue fluids and
fine-needle aspirations can be useful adjuncts to smears
for establishing a more definitive cytopathologic
diagnosis. They can be particularly useful for
categorization of tumors that otherwise may not be
possible from smears themselves. A modified cell block
technique using an improvised ethanol formalin fixative
(Nathan alcohol formalin substitute) followed by a
simple paraffin processing schedule is described. This
improved preparation offers excellent cytomorphologic
features corresponding closely to cells in
Papanicolaou-stained smears and ensures optimal
preservation of histochemical and immunocytochemical
properties. The technique is simple and reproducible
and uses routine safe laboratory chemicals. The efficacy
of cell blocks also is discussed.
The use of cell blocks in routine nongynecologic
cytopathology varies in each institution. Despite the
increased use of fine-needle aspiration cytology (FNAC)
and immunocytochemistry in the diagnosis of solid tumors,
only limited information is available to assess the contribution
of cell blocks, although the value of cell blocks has
been acknowledged.1,2 Several techniques also have been
reported that vary in scope and the type of fixatives and
embedding techniques used, making valid comparison
difficult.1-8
Most methods previously described are inconvenient or
time consuming in a routine active pathology laboratory and
include using chemicals that have hazardous potential. In
addition, except for mercuric chloride–based fixatives, most
do not offer the optimal morphologic characterization of
cells compared with corresponding smears.
This article reports a 2-year study of a cell block preparation
arising from the need to replace the excellent but
highly hazardous B-5 mercury fixative,9 which had been
very successful in our hands. The development for a suitable
alternative, aimed at achieving the following basic
cytologic expectations, was undertaken: (1) the cells closely
resemble corresponding cells in alcohol-fixed Papanicolaou-stained
smears; (2) there is adequate clarity and delineation
of nuclear and cytoplasmic details; (3) loose cells,
cell aggregates, and microscopic tissue fragments are easily
recoverable; (4) the cell block sections are suited to a wide
variety of histochemical stains and immunocytochemistry;
(5) the method is simple, reproducible, and readily adaptable
in a routine hospital laboratory; and (6) the final cell
morphology in paraffin sections is no less than in B-5–fixed
sections. The contribution of cell blocks in the final diagnosis
using this method of preparation also was evaluated.
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