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| Main Authors: | , , , , , , , , |
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| Format: | Artículo Open Access |
| Published: |
Wiley
2026
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| Online Access: | https://pathsocjournals.onlinelibrary.wiley.com/doi/10.1002/path.70038 |
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- Bile duct tumor thrombus (intraductal polypoid growth)–positive intrahepatic cholangiocarcinoma: clinicopathologic and genomic analysis Ayaka Mitsui Minoru Esaki Satoshi Nara Yasuhito Arai Hiromi Nakamura Tatsuhiro Shibata Daisuke Ban Takahiro Mizui Nobuyoshi Hiraoka The Journal of Pathology Abstract Bile duct tumor thrombus (BDTT), a tumor cluster occupying the luminal space in the large bile duct, is rare in intrahepatic cholangiocarcinoma (iCCA). Most studies on BDTT in iCCA to date are case reports, and the clinicopathological characteristics remain unknown. This study aimed to characterize iCCA with BDTT clinicopathologically and genetically. We analyzed 223 surgically resected iCCA cases, including 102 small duct type (SDT) and 121 large duct type (LDT) cases. BDTT was found in 19.6% (20/102) of SDT cases. Histological and immunohistochemical features of BDTT‐positive SDT were comparable with those of conventional SDT (MUC1 + MUC2 − MUC5AC − MUC6 +/− CDX‐2 − ). BDTT‐positive SDT showed female predominance and higher T factors compared with conventional SDT. SDT was associated with a significantly longer survival in iCCA. SDT patients with BDTT had significantly shorter survival than those without BDTT and survival rates similar to those of LDT patients; the presence of BDTT in SDT was an independent unfavorable prognostic factor (HR = 2.601, p = 0.006). Whole‐exome sequencing analysis revealed recurrent altered gene expression: those more frequent in SDT compared with LDT ( BAP1 , IDH1/2 , ZNF717 , FGFR2 , NRAS ); those more frequent in LDT ( KRAS , TP53 , SMAD4 , MUC6 , CACNA1A , MLL2 , MDM2 , TGFBR1/2) ; and those found comparably in both SDT and LDT ( MUC4 , ARID1A , EPHA2 , PIK3CA , MUC17 , MAP3K4 , MUC2 , BRAF , NF1 ). Genetic landscapes were similar in SDT iCCA with and without BDTT; recurrent mutations in MUC2 and MUC17 and FGFR2 fusion genes were more frequent in BDTT‐positive SDTs. PTPRK :: RSPO3 fusion gene was found in one LDT case. Intraglandular papillary and tubular proliferation is a unique and rare histology of SDT. BDTT was frequently found in SDT with this pattern, and FGFR2 gene rearrangement was frequent. These results highlight the importance of evaluating BDTT in SDT, as it may be the main route of hilar extension in aggressive cases. © 2026 The Pathological Society of Great Britain and Ireland. 10.1002/path.70038 http://onlinelibrary.wiley.com/termsAndConditions#vor