Uterine intravascular adenomyomatosis: Clinicopathological features and literature review of a rare entity

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AI-generated summary by claude@2026-07, 2026-07-25

This case report describes a rare instance of uterine intravascular adenomyomatosis in a 45-year-old woman, characterized by endometrial glands within myometrial vessels, and reviews 11 similar benign cases from the literature.

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Abstract

BACKGROUND: Intravascular adenomyomatosis (IA), characterised by endometrial-type glands or stroma embedded within smooth muscle tissue inside myometrial vessels, is a rare variant within the spectrum of uterine intravenous leiomyomatosis (IVL). CASE REPORT: A 45-year-old nulligravid woman presented with hypermenorrhoea and a large uterine mass radiologically interpreted as a degenerated fibroid. Histopathological examination of the hysterectomy specimen revealed a cellular leiomyoma with smooth muscle fibres and endometrial-type stroma within CD31-lined myometrial vessels, showing low mitotic activity and no atypia or necrosis. The postoperative course was uneventful, and the patient remained disease-free 12 months after surgery. DISCUSSION: Although IA is a benign lesion, intravascular growth may mimic malignancy both radiologically and histologically. A comprehensive review of the literature identified only 11 reported cases, most diagnosed postoperatively, all showing benign behaviour after complete excision. Awareness of this condition may prevent overtreatment and misclassification.

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MeSH descriptors

Leiomyomatosis Leiomyomatosis Leiomyomatosis Leiomyomatosis Leiomyomatosis Leiomyomatosis Leiomyomatosis Leiomyomatosis Leiomyomatosis Leiomyomatosis Leiomyomatosis Leiomyomatosis Uterine Neoplasms Uterine Neoplasms Uterine Neoplasms Uterine Neoplasms Uterine Neoplasms Uterine Neoplasms Uterine Neoplasms Uterine Neoplasms

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europepmc
last seen: 2026-07-29T06:27:48.050232+00:00
pubmed
last seen: 2026-07-29T06:22:14.364230+00:00
unpaywall
last seen: 2026-05-11T08:34:28.763810+00:00
License: CC-BY-4.0 · commercial use OK · attribution required
Courtesy of the U.S. National Library of Medicine