StayCurrentMD · Prospective evaluation of common hepatic duct histopathology at the time of choledochal cyst excision ranging from children to adults
Article1 min read·Published Nov 2023Older

Prospective evaluation of common hepatic duct histopathology at the time of choledochal cyst excision ranging from children to adults

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Article · Nov 2023 · 1 min read

In brief

In brief

Prospective histopathologic study of 65 choledochal cyst patients (children and adults) reveals higher mucosal damage and inflammation in pediatric cases, with dysplasia identified in a 4-month-old infant. Findings suggest children face significant malignancy risk requiring meticulous histologic evaluation and long-term surveillance.

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Abstract

Purpose

To evaluate common hepatic duct just distal to the HE anastomosis (d-CHD) prospectively for mucosal damage, inflammation, fibrosis, dysplasia, carcinoma in situ, malignant transformation, effects of serum amylase, and symptoms at presentation in CC cases ranging from children to adults.

Methods

Cross-sections of d-CHD obtained at cyst excision 2018–2023 from 65 CC patients; 40 children (< 15 years old), 25 adults (≥ 15) were examined with hematoxylin and eosin, Ki-67, S100P, IMP3, p53, and Masson’s trichrome to determine an inflammation score (IS), fibrosis score (FS), and damaged mucosa rate (DMR; damaged mucosa expressed as a percentage of the internal circumference).

Results

Mean age at cyst excision (“age”) was 18.2 years (range: 3 months-74 years). Significant inverse correlations were found for age and DMR (p = 0.002), age and IS (p = 0.011), and age and Ki-67 (p = 0.01). FS did not correlate with age (p = 0.32) despite significantly increased IS in children. Dysplasia was identified in a 4-month-old girl with cystic CC. Serum amylase was elevated in high DMR subjects.

Conclusions

High DMR, high IS, and evidence of dysplasia in pediatric CC suggest children are at risk for serious sequelae best managed by precise histopathology, protocolized follow-up, and awareness that premalignant histopathology can arise in infancy.

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