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Histopathological growth pattern and vessel co-option in intrahepatic cholangiocarcinoma.

Authors :
Li, Zihan
Nguyen Canh, Hiep
Takahashi, Kenta
Le Thanh, Dong
Nguyen Thi, Quynh
Yang, Rui
Yoshimura, Kaori
Sato, Yasunori
Nguyen Thi, Khuyen
Nakata, Hiroki
Ikeda, Hiroko
Kozaka, Kazuto
Kobayashi, Satoshi
Yagi, Shintaro
Harada, Kenichi
Source :
Medical Molecular Morphology. Sep2024, Vol. 57 Issue 3, p200-217. 18p.
Publication Year :
2024

Abstract

Intrahepatic cholangiocarcinoma (iCCA) exhibits different blood imaging features and prognosis depending on histology. To clarity histopathological growth patterns (HGPs) and vascularization processes of iCCA, we collected 145 surgical specimens and histologically classified them into large bile duct (LBD) (20 cases), small bile duct (SBD) (54), cholangiolocarcinoma (CLC) (35), combined SBD–CLC (cSBD–CLC) (26), and ductal plate malformation (DPM) (10) (sub)types. According to the invasive pattern at the interface between tumor and adjacent background liver, HGPs were classified into desmoplastic, pushing, and replacing HGPs. Desmoplastic HGP predominated in LBD type (55.5%), while replacing HGP was common in CLC (82.9%) and cSBD–CLC (84.6%) subtypes. Desmoplastic HGP reflected angiogenesis, while replacing HGP showed vessel co-option in addition to angiogenesis. By evaluating microvessel density (MVD) using vascular markers, ELTD1 identified vessel co-option and angiogenesis, and ELTD1-positive MVD at invasive margin in replacing HGP was significantly higher than those in desmoplastic and pushing HGPs. REDD1, an angiogenesis-related marker, demonstrated preferably higher MVD in the tumor center than in other areas. iCCA (sub)types and HGPs were closely related to vessel co-option and immune-related factors (lymphatic vessels, lymphocytes, and neutrophils). In conclusion, HGPs and vascular mechanisms characterize iCCA (sub)types and vessel co-option linked to the immune microenvironment. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
18601480
Volume :
57
Issue :
3
Database :
Academic Search Index
Journal :
Medical Molecular Morphology
Publication Type :
Academic Journal
Accession number :
179232548
Full Text :
https://doi.org/10.1007/s00795-024-00392-1