A detailed comparison between the endoscopic images using blue laser imaging and three-dimensional reconstructed pathological images of colonic lesions.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2020
Historique:
received: 14 02 2020
accepted: 12 06 2020
entrez: 30 6 2020
pubmed: 1 7 2020
medline: 4 9 2020
Statut: epublish

Résumé

Blue laser/light imaging (BLI) is an image-enhanced endoscopy (IEE) technique that can provide an accurate diagnosis by closely observing the surface structure of various colonic lesions. However, complete correspondence between endoscopic images and pathological images has not been demonstrated. The aim of this study was to accurately compare endoscopic images and the pathological images using a three-dimensionally (3D) reconstructed pathological model. Continuous thin layer sections were prepared from colonic tissue specimens and immunohistochemically stained for CD34 and CAM5.2. Three-dimensional reconstructed images were created by superimposing immunohistochemically stained pathological images. The endoscopic image with magnifying BLI was compared with the top view of the 3D reconstructed image to identify any one-to-one correspondence between the endoscopic images and histopathological images using the gland orifices and microvessels as a guide. Using 3D reconstructed pathological images, we were able to identify the location on the endoscope image in cases of colonic adenocarcinoma, adenoma and normal mucosa. As a result, the horizontal plane of the endoscopic image and the vertical plane of the 2D pathological specimen were able to be compared, and we successfully determined the visible blood vessel depth and performed a detailed evaluation on magnifying BLI. Examples are as follows: (1) The median vasculature depth from the mucosal surface that could be recognized as vasculature on magnifying BLI was 29.4 μm. The median depth of unrecognizable vessels on magnifying BLI was 218.8 μm, which was significantly deeper than recognizable vessels. (2) Some brownish structures were suggested to potentially be not only dense vessels, vessel expansions, corrupted vessels but also bleeding or extravasation of erythrocytes. Overall, we demonstrated a new approach to matching endoscopic images and pathological findings using a 3D-reconstructed pathological model immunohistochemically stained for CD34 and CAM5.2. This approach may increase the overall understanding of endoscopic images and positively contribute to making more accurate endoscopic diagnoses.

Identifiants

pubmed: 32598341
doi: 10.1371/journal.pone.0235279
pii: PONE-D-20-04430
pmc: PMC7323971
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0235279

Déclaration de conflit d'intérêts

The authors of this paper have read the journal's policy and have the following competing interests to declare: Yuichi Teramura is an employee of Clinical Research Endoscopy System Division and Medical System Business Division, FUJIFILM Corporation. This does not alter our adherence to PLOS ONE policies on sharing data and materials. There are no patents, products in development or marketed products associated with this research to declare.

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Auteurs

Takeshi Ueda (T)

Department of Surgery, Nara Medical University, Kashihara, Japan.
Department of Surgery, Minami-Nara General Medical center, Yoshino, Nara, Japan.

Kohei Morita (K)

Department of Diagnostic Pathology, Nara Medical University, Kashihara, Japan.

Fumikazu Koyama (F)

Department of Surgery, Nara Medical University, Kashihara, Japan.
Department of Endoscopy, Nara Medical University Hospital, Kashihara, Japan.

Yuichi Teramura (Y)

Clinical Research Endoscopy System Division and Medical System Business Division, FUJIFILM Corporation, Tokyo, Japan.

Tadashi Nakagawa (T)

Department of Surgery, Saiseikai Chuwa Hospital, Sakurai, Japan.

Shinji Nakamura (S)

Department of Surgery, Takanohara Central Hospital, Nara, Japan.

Yayoi Matsumoto (Y)

Department of Surgery, Nara Medical University, Kashihara, Japan.

Takashi Inoue (T)

Department of Surgery, Nara Medical University, Kashihara, Japan.

Takayuki Nakamoto (T)

Department of Surgery, Nara Medical University, Kashihara, Japan.
Department of Endoscopy, Nara Medical University Hospital, Kashihara, Japan.

Yoshiyuki Sasaki (Y)

Department of Surgery, Nara Medical University, Kashihara, Japan.

Hiroyuki Kuge (H)

Department of Surgery, Nara Medical University, Kashihara, Japan.

Maiko Takeda (M)

Department of Diagnostic Pathology, Nara Medical University, Kashihara, Japan.

Chiho Ohbayashi (C)

Department of Diagnostic Pathology, Nara Medical University, Kashihara, Japan.

Hisao Fujii (H)

Gastrointestinal Endoscopy and IBD center, Yoshida Hospital, Nara, Japan.

Masayuki Sho (M)

Department of Surgery, Nara Medical University, Kashihara, Japan.

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