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Improving histological assessment of intraductal extension in papillary adenomas by guidewire cannulation of the ex vivo specimen
Poster Abstract

Aims

Endoscopic papillectomy (EP) is an effective treatment for papillary adenomas, but intraductal extension (IDE) is a known risk factor for incomplete resection and recurrence. Accurate histological assessment of IDE is often challenging due to specimen orientation. We evaluated whether ex-vivo guidewire cannulation of specimens improved histological assessment.

Methods

Consecutive Patients undergoing EP with ex-vivo guidewire cannulation of major papilla at a tertiary centre over 30 months, to Oct 2025 were included. Specimens with non-adenomatous histopathology were excluded. Propensity score matching (1:1) was performed for size, en-bloc resection, and laterally spreading component (LSL) against a prior cohort. Outcomes included histological identification of the biliary duct orifice and intraductal extension.

Results

60 patients were included, 30 with ex-vivo guidewire cannulation (wired) and 30 propensity-matched controls without guidewire (non-wired). The groups were balanced for age (mean 64 years), sex (16 males per group), median lesion size (25 mm), en-bloc resection (21 per group), and lateral spreading component >10 mm (12 per group). Histopathology comprised tubular adenomas with low-grade dysplasia (LGD) in 38 patients (20 wired, 18 non-wired), tubulovillous adenomas with LGD in 15 (10 wired, 5 non-wired), high-grade tubulovillous adenomas in 2 (1 wired, 1 non-wired), and carcinoma in 9 (5 wired, 4 non-wired). The common bile duct orifice was identified in 23/30 (77%) wired versus 13/30 (43%) non-wired specimens (p = 0.017), and histologic intraductal extension was detected in 17/30 (57%) wired versus 10/30 (33%) non-wired specimens (p = 0.119).

Conclusions

Ex-vivo guidewire cannulation of papillary specimens improved identification of the CBD orifice by 33% and nearly doubled the detection of intraductal adenoma. This technique allows identification of a subgroup at risk of intraductal recurrence, the primary means by which papillary adenomas reoccur. These findings have important implications for subsequent surveillance and therapy.