Glinkova · Gut 2004 · prospective cohort study · n=94

Hepatic haemangiomas: possible association with female sex hormones.

Cited 170 times in the scientific literature.

Level 3 - non-randomized controlled study

Prospective non-randomized cohort study

PubMed 15306599 · doi:10.1136/gut.2003.038646 · record verified 2026-08-29

What was done

A prospective cohort study followed 94 women with 181 ultrasound-diagnosed hepatic haemangiomas for 1 to 17 years (mean 7.3 years, standard deviation 5.5). Lesion location, number, size, and ultrasonographic pattern were monitored over time. Participants completed questionnaires regarding gynaecological and reproductive history, and changes in haemangioma number and size were compared between 22 patients receiving exogenous hormone therapy and 72 unexposed controls.

What was found

Age at first period was inversely correlated with haemangioma size (r = 0.181, p = 0.015), and age at menopause was positively correlated with the number of baseline haemangiomas (r = 0.542, p < 0.0001). Lesion enlargement occurred in 5 of 22 (22.7%) hormone therapy users compared to 7 of 72 (9.7%) unexposed controls. Three variables independently predicted lesion growth: hormone therapy (p = 0.05), a hypoechoic pattern versus a hyperechoic pattern (p = 0.003), and a lower total number of haemangiomas at baseline (p = 0.006). No changes in lesion count or ultrasound pattern occurred during follow-up.

Why it matters

This study provides prospective evidence that both endogenous and exogenous female sex hormones can influence hepatic haemangioma natural history, supporting periodic ultrasound monitoring for women on hormone therapy.

Limits

The total sample size was small with only 22 hormone-exposed patients and 12 total progression events across the entire cohort. Follow-up duration varied widely from 1 to 17 years. The abstract does not detail specific hormone regimens, dosages, indications for therapy, or control for potential baseline confounders between groups.

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