Hypodermic needle without recipient paraffin block technique.

This technique allows building TMA blocks with more than 300 tissue cores without using a recipient paraffin block for the tissue cores and without using a commercial TMA builder instrument. It is based on the construction of TMA needles modifying conventional hypodermic needles to punch tissue cores from donor blocks. Tissue cores are punctured from donor blocks and attached by double-sided adhesive tape on a computer-generated paper grid used to align the cores on the block mold, which is filled with liquid paraffin. TMA blocks constructed using this method can be utilized as positive and negative controls for immunohistochemistry, histochemistry and other techniques, interlaboratory quality control and also in research, but never for diagnosis purposes. This technique has the following advantages: it is easy to reproduce, affordable, quick, and creates uniform blocks with more than 300 cores aligned, at the same plane, adherent, and easy to cut, with negligible losses during conventional cutting and technical procedures.

TMA for all: a new method for the construction of tissue microarrays without recipient paraffin block using custom-built needles.

BACKGROUND: TMAs are becoming a useful tool for research and quality control methods, mostly for immunohistochemistry and in situ hybridization. METHODS: A new technique that allows building TMA blocks with more than 300 tissue cores without using a recipient paraffin block for the tissue cores and without using a commercial TMA builder instrument is described. This technique is based on the construction of TMA needles modifying conventional hypodermic needles to punch tissue cores from donor blocks, which are attached by double-side adhesive tape on a computer-generated paper grid used to align the cores on the block mould, which is filled with liquid paraffin. RESULTS: More than two hundred TMA blocks were constructed using this method, utilized in immunohistochemistry and histochemistry as positive and negative controls and also in research. CONCLUSION: This technique has the following advantages: it is easy to reproduce, affordable, quick and creates uniform blocks with more than 300 cores aligned, adherent and easy to cut, with negligible losses during cutting and immunohistochemistry and in situ hybridization procedures.