Diagnostic significance of apical membranous and cytoplasmic dot-like CD26 expression in encapsulated follicular variant of papillary thyroid carcinoma: a useful marker for capsular invasion.


Journal

Endocrine journal
ISSN: 1348-4540
Titre abrégé: Endocr J
Pays: Japan
ID NLM: 9313485

Informations de publication

Date de publication:
28 Dec 2020
Historique:
pubmed: 4 9 2020
medline: 15 10 2021
entrez: 4 9 2020
Statut: ppublish

Résumé

Non-invasive follicular thyroid neoplasm with papillary-like nuclear features (NIFTP) and invasive encapsulated follicular variant of papillary thyroid carcinoma (EFV-PTC) are indistinguishable preoperatively. CD26 expression in follicular tumor-uncertain malignant potential (FT-UMP) is reported to be clearly higher than in that without capsular invasion. To verify the diagnostic significance of CD26 immunostaining in EFV-PTC, we examined the expression pattern of CD26 in non-invasive EFV-PTC (NIFTP) and invasive EFV-PTC. We performed immunohistochemical analysis using CD26 antibody for 37 NIFTPs and 54 EFV-PTCs (34 minimally invasive EFV-PTCs and 20 widely invasive EFV-PTCs). Most NIFTP samples showed an apical membranous pattern or a cytoplasmic diffuse pattern of expression. Invasive EFV-PTCs more frequently showed a cytoplasmic dot-like pattern, and the labeling indices of tumor cells with cytoplasmic dot-like patterns were significantly higher than those in NIFTPs. The sizes of dots seen in NIFTPs (mean: 1.12 μm) were significantly smaller than in invasive EFV-PTCs (1.33 μm), minimally invasive EFV-PTC (1.27 μm), and widely invasive EFV-PTC (1.38 μm). We, therefore, conclude that cytoplasmic diffuse and/or cytoplasmic dot-like CD26 expression, particularly the larger CD26-positive dots, could be useful markers for capsular invasion in EFV-PTC. CD26 immunostaining, using cell blocks or cytological specimens, may preoperatively distinguish between NIFTP and invasive EFV-PTC.

Identifiants

pubmed: 32879160
doi: 10.1507/endocrj.EJ19-0501
doi:

Substances chimiques

Biomarkers, Tumor 0
Dipeptidyl Peptidase 4 EC 3.4.14.5

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1207-1214

Auteurs

Shoji Takagi (S)

Department of Medical Life Science, Kurashiki University of Science and the Arts, Kurashiki, Okayama 712-8505, Japan.
Faculty of Medicine, Graduate School of Medicine, Kagawa University, Miki, Kagawa 761-0793, Japan.

Mitsuyoshi Hirokawa (M)

Department of Diagnostic Pathology and Cytology, Kuma Hospital, Kobe, Hyogo 650-0011, Japan.

Kenji Nagashima (K)

Department of Clinical Laboratory, Gifu University Hospital, Gifu, Gifu 501-1194, Japan.

Miyoko Higuchi (M)

Department of Diagnostic Pathology and Cytology, Kuma Hospital, Kobe, Hyogo 650-0011, Japan.

Kyuichi Kadota (K)

Department of Diagnostic Pathology, Faculty of Medicine, Kagawa University, Miki, Kagawa 761-0793, Japan.

Ryou Ishikawa (R)

Department of Diagnostic Pathology, Faculty of Medicine, Kagawa University, Miki, Kagawa 761-0793, Japan.

Masakazu Sato (M)

Department of Medical Life Science, Kurashiki University of Science and the Arts, Kurashiki, Okayama 712-8505, Japan.

Akira Miyauchi (A)

Department of Surgery, Kuma Hospital, Kobe, Hyogo 650-0011, Japan.

Yasuyuki Miyake (Y)

Department of Medical Life Science, Kurashiki University of Science and the Arts, Kurashiki, Okayama 712-8505, Japan.

Reiji Haba (R)

Department of Diagnostic Pathology, Faculty of Medicine, Kagawa University, Miki, Kagawa 761-0793, Japan.

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Classifications MeSH