Podcast
Questions and Answers
What is the purpose of decalcification in the specimen preparation process?
What is the purpose of decalcification in the specimen preparation process?
Which of the following acids is NOT commonly used as a decalcifying agent in histology?
Which of the following acids is NOT commonly used as a decalcifying agent in histology?
Why does the specimen need to be dehydrated before being infiltrated with wax?
Why does the specimen need to be dehydrated before being infiltrated with wax?
What does it mean for paraffin wax to be hydrophobic?
What does it mean for paraffin wax to be hydrophobic?
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When should decalcification be performed during the specimen preparation process?
When should decalcification be performed during the specimen preparation process?
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What effect does high temperature have on tissue during processing?
What effect does high temperature have on tissue during processing?
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How does low temperature impact the viscosity of reagents during tissue processing?
How does low temperature impact the viscosity of reagents during tissue processing?
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In what condition should embedding waxes be maintained for optimal tissue processing?
In what condition should embedding waxes be maintained for optimal tissue processing?
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What is the impact of reduced pressure on tissue processing?
What is the impact of reduced pressure on tissue processing?
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How does high pressure affect dense specimens during tissue processing?
How does high pressure affect dense specimens during tissue processing?
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Why is it important to prevent tissues from being packed too tightly in baskets during processing?
Why is it important to prevent tissues from being packed too tightly in baskets during processing?
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What should be done if the specimen is unlabeled or the information in the requisition form is incomplete?
What should be done if the specimen is unlabeled or the information in the requisition form is incomplete?
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What does the accession number represent in tissue processing?
What does the accession number represent in tissue processing?
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When should tissues be fixed after arriving in the laboratory?
When should tissues be fixed after arriving in the laboratory?
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Which of the following is NOT a purpose of fixation with formaldehyde/formalin?
Which of the following is NOT a purpose of fixation with formaldehyde/formalin?
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What information does the code 'S-19-0001' convey about a specimen?
What information does the code 'S-19-0001' convey about a specimen?
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What should all materials included in a specimen be labeled with?
What should all materials included in a specimen be labeled with?
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What is a disadvantage of using liquid nitrogen in histochemistry procedures?
What is a disadvantage of using liquid nitrogen in histochemistry procedures?
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How can the issue of uneven cooling and difficult diagnostic interpretation be overcome when using liquid nitrogen?
How can the issue of uneven cooling and difficult diagnostic interpretation be overcome when using liquid nitrogen?
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How is liquid nitrogen used in combination with Isopentane for tissue freezing?
How is liquid nitrogen used in combination with Isopentane for tissue freezing?
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Which method involves using conventional CO2 gas for freezing tissue?
Which method involves using conventional CO2 gas for freezing tissue?
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What is the purpose of aerosol sprays in tissue freezing procedures?
What is the purpose of aerosol sprays in tissue freezing procedures?
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What can happen if urgent blocks are overcooled during sectioning at -70°C or below?
What can happen if urgent blocks are overcooled during sectioning at -70°C or below?
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What is the most important step in embedding tissue for sectioning?
What is the most important step in embedding tissue for sectioning?
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Why is it important for the wax in the mold to solidify?
Why is it important for the wax in the mold to solidify?
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What effect does good infiltration of wax have on tissue?
What effect does good infiltration of wax have on tissue?
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What is the purpose of transferring tissue to a mold filled with molten wax?
What is the purpose of transferring tissue to a mold filled with molten wax?
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Why is it important to wait for the wax to solidify at 20°C after embedding tissue?
Why is it important to wait for the wax to solidify at 20°C after embedding tissue?
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What is the purpose of trimming and cutting embedded tissue into thin slices using a microtome?
What is the purpose of trimming and cutting embedded tissue into thin slices using a microtome?
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Study Notes
Decalcification in Specimen Preparation
- Decalcification removes calcium deposits from tissues, facilitating easier sectioning and improving staining quality.
- Common acids for decalcification include nitric acid, formic acid, and EDTA; however, hydrochloric acid is NOT commonly used.
Dehydration and Infiltration with Wax
- Dehydration removes water to allow proper infiltration of paraffin wax.
- Paraffin wax is hydrophobic, meaning it repels water, making dehydration necessary for effective embedding.
Timing and Temperature in Decalcification
- Decalcification should be done after fixation and before dehydration and embedding to preserve tissue integrity.
- High temperatures can cause tissue shrinkage and degradation during processing.
Effects of Temperature and Pressure on Processing
- Low temperatures increase reagent viscosity, hindering the movement of fluids through tissue.
- Reduced pressure can enhance tissue infiltration by allowing better penetration of reagents.
- High pressure can lead to distortion in dense specimens, making them difficult to process effectively.
Specimen Handling and Labeling
- Tissues should not be packed too tightly in baskets to ensure adequate reagent flow and avoid processing artifacts.
- Unlabeled specimens or incomplete requisition forms should be clarified with the sender or properly documented before processing.
- The accession number is a unique identifier for tracking specimens throughout the laboratory process.
Fixation and Specimen Information
- Tissues should be fixed immediately upon arrival in the laboratory to prevent degradation.
- Formaldehyde/formalin fixation is NOT aimed at maintaining tissue color; its primary purposes include preserving cellular structure and preventing autolysis.
Specimen Labeling and Storage
- All materials in a specimen should be labeled with the patient's identification information, including accession number and specimen type.
- Liquid nitrogen use in histochemistry can lead to uneven cooling, impacting diagnostic results, but using Isopentane helps to achieve more uniform cooling.
Freezing and Cutting Procedures
- CO2 gas can be used for freezing tissue in place of liquid nitrogen.
- Aerosol sprays can enhance tissue freezing by rapidly taking heat away.
- Overcooling urgent blocks at -70°C or below can result in brittle sections that are difficult to obtain.
Embedding and Sectioning
- The most critical step in embedding is ensuring proper infiltration with wax, which enhances tissue integrity.
- Solidifying the wax in the mold maintains tissue architecture and prevents distortion during cutting.
- Good infiltration ensures fine details in the tissue are preserved for accurate diagnosis.
- Transferring tissue to a mold filled with molten wax helps create stable specimens for easier sectioning.
- Wax must solidify at around 20°C to ensure proper tissue embedding, enabling precision cutting with a microtome.
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Description
This quiz tests your knowledge on labelling complete request forms for patient information, history, and tissue site of origin. It also covers the rules for tissue accessioning, including codes for different types of specimens and how to create unique accession numbers.