2010
DOI: 10.1136/jcp.2010.078980
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New double embedding technique for specimens of endoscopic submucosal dissection using agarose: comparison with other media

Abstract: The present new double embedding technique using agarose provides not only an easy and reliable embedding procedure for technicians but also accurate and exact diagnosis for pathologists.

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Cited by 6 publications
(9 citation statements)
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“…In the next few decades, many types of media were used to wrap larger ESD specimens to hold the tissues in place 30 31. In other studies,20 double embedding technique was carried out for larger tissues obtained by the ESD procedure. In the first-step embedding, agarose, agar and gelatin were all applied as embedding medium for covering ESD specimens and cutting the tissues with medium, so as to avoid tissue shrinking and hold the specimens in place without moving in the cassette during processing.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…In the next few decades, many types of media were used to wrap larger ESD specimens to hold the tissues in place 30 31. In other studies,20 double embedding technique was carried out for larger tissues obtained by the ESD procedure. In the first-step embedding, agarose, agar and gelatin were all applied as embedding medium for covering ESD specimens and cutting the tissues with medium, so as to avoid tissue shrinking and hold the specimens in place without moving in the cassette during processing.…”
Section: Discussionmentioning
confidence: 99%
“…Ten pathology technicians/pathologists involved in this study. The design of this questionnaire borrowed the contents of the previous study 20…”
Section: Methodsmentioning
confidence: 99%
“…The older literature from the 1960s, 1970s and 1980s proposed a pre-embedding technique in agar to maintain the precise orientation of tissue specimens before paraffin embedding 1–4. Advantages in microtome section preparation have been well documented in small tissue biopsies,7–9 ocular biopsies,10 skin samples11 12 and large dissection specimens 13. Unfortunately, even though often used in cytology14 and biology/botany,15 this technique is by no means widespread in routine pathology laboratories as it requires instrumentation, all be it simple, and lengthens cut up time.…”
Section: Discussionmentioning
confidence: 99%
“…All specimens were completely dissected into 2- to 3-mm thick slices. Then, 3-μm sections from each slice were examined with hematoxylin and eosin (HE) or Elastica van Gieson staining [ 13 ]. Immunohistochemistry for desmin and D2-40 was performed to visualize muscularis mucosae and lymphatic vessels, respectively [ 13 ].…”
Section: Methodsmentioning
confidence: 99%