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Freezing Ballantine smear inspection

A detection method and freezing technology, which is applied in the preparation of test samples, medical science, ovulation diagnosis, etc., can solve the problems of incomplete collection of cells, complicated technical operations, poor nuclear plasma staining, etc., and is conducive to comprehensive promotion , Clarity of boundary, effect of clear nucleoplasm and cell components

Inactive Publication Date: 2006-11-01
佛山市顺德区桂洲医院
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Problems solved by technology

But it still has the following disadvantages: 1), cell collection is not comprehensive, smear cells overlap, after application of high-concentration ethanol or ethanol ethyl ether mixed fixative, cell shrinkage is obvious, mucus denaturation is solidified, and staining agent is difficult for penetrating mucus in the staining process Denatured membranes lead to poor staining of mucus-wrapped cells and poor nuclear plasma staining, especially when the smear is thick and the cell resolution is poor in areas with significant cell overlap, which seriously affects observation and easily leads to missed diagnosis and misdiagnosis; 2) when fixed cells If the staining is not done in time, the cells are easily deformed, and the subsequent staining effect will be seriously affected
For this reason, although medical experts have successively invented a variety of cytological improvement techniques, which have a certain effect on solving some defects of traditional Pap smears, such as TCT, LCT, LPT and other techniques, but these techniques are complicated to operate and require special equipment and special tools. Consumables are expensive, difficult to popularize, and have great limitations in practical applications, especially when performing large-scale cell smears, the above-mentioned technical defects are more prominent

Method used

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Experimental program
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Embodiment Construction

[0018] Frozen type Pap smear detection method, comprises the following steps:

[0019] a), first collect cell samples at the cervix with a cell-specific sampler;

[0020] b), and then smear the cell sample collected by the sampler on a clean glass slide;

[0021] c), and then place the above-mentioned glass slides coated with cell samples in the mixed fixation solution of acetic acid ethanol, and take out after the cell samples on the glass slides are fixed;

[0022] d), immerse the cell sample on the above-mentioned removed glass slide in the cell denaturation recovery solution for 1-5 minutes, and take it out;

[0023] e), and then put the above-mentioned glass slides into a freezer to freeze, so that the water infiltrated in the cell sample forms ice crystals;

[0024] f) Finally, take out the slide with the cell sample that has been frozen, and directly perform HE staining or Pap smear staining at room temperature, and observe and diagnose under a microscope.

[0025] A...

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Abstract

A method for detecting Pasteur smear of frozen type includes using sampler to collect cell sample from neck of uterus and coating collected cell sample on clean glass plate, placing said glass plate in fixing liquid of aceto-alcohol and taking glass plate out after cell sample is fixed, soaking said glass plate on cell denaturation recovery liquid for 1-5 min., taking it out then placing it in freezer for refrigerating to make water content in cell sample be formed to be ice crystal, taking it out to carry out HE stain on it at normal temperature then making observation and diagnosis under microscope.

Description

technical field [0001] The invention relates to a frozen Pap smear detection method. Background technique [0002] At present, the traditional Pap smear technology has been used for nearly 50 years, and has made an extremely important contribution to the prevention and treatment of cervical cancer worldwide. The method it adopts is to use samplers such as cotton swabs and scrapers to collect cell samples from the cervix, directly smear them on glass slides, fix them in time, and then stain them directly. Although it is simple, quick and cheap. But it still has the following disadvantages: 1), cell collection is not comprehensive, smear cells overlap, after application of high-concentration ethanol or ethanol ethyl ether mixed fixative, cell shrinkage is obvious, mucus denaturation is solidified, and staining agent is difficult for penetrating mucus in the staining process Denatured membranes lead to poor staining of mucus-wrapped cells and poor nuclear plasma staining, esp...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): G01N1/28A61B10/00
Inventor 毛荣军
Owner 佛山市顺德区桂洲医院