Evidence map›Paper›PMID 40539160›Full record

ArticleCureus2025

Intravenous Leiomyomatosis: The Importance of an Early Diagnosis.

Tânia Boto, Catarina Magalhães Silva, Sofia Morgado Oliveira, Mariana Pereira Pinto, António Ribeiro Vieira, Carolina Piloto Lemos, Diana Neves Correia, Joana Albuquerque, Isabela Queimadela, Filipa Garcez Fernandes

Abstract readCase Reports
In one paragraph

Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Tânia BotoFamily and Community Medicine, Unidade de Saúde Familiar (USF) Infante D. Henrique (Family Health Unit Infante D. Henrique), Viseu, PRT.
Catarina Magalhães SilvaFamily and Community Medicine, Unidade de Saúde Familiar (USF) Infante D. Henrique (Family Health Unit Infante D. Henrique), Viseu, PRT.
Sofia Morgado OliveiraFamily and Community Medicine, Unidade de Saúde Familiar (USF) Leiria Nascente (Family Health Unit Leiria Nascente), Leiria, PRT.
Mariana Pereira PintoFamily and Community Medicine, Unidade de Saúde Familiar (USF) Infante D. Henrique (Family Health Unit Infante D. Henrique), Viseu, PRT.
António Ribeiro VieiraFamily and Community Medicine, Unidade de Saúde Familiar (USF) Infante D. Henrique (Family Health Unit Infante D. Henrique), Viseu, PRT.
Carolina Piloto LemosFamily and Community Medicine, Unidade de Saúde Familiar (USF) Infante D. Henrique (Family Health Unit Infante D. Henrique), Viseu, PRT.
Diana Neves CorreiaFamily and Community Medicine, Unidade de Saúde Familiar (USF) Infante D. Henrique (Family Health Unit Infante D. Henrique), Viseu, PRT.
Joana AlbuquerqueFamily and Community Medicine, Unidade de Saúde Familiar (USF) Infante D. Henrique (Family Health Unit Infante D. Henrique), Viseu, PRT.
Isabela QueimadelaFamily and Community Medicine, Unidade de Saúde Familiar (USF) Infante D. Henrique (Family Health Unit Infante D. Henrique), Viseu, PRT.
Filipa Garcez FernandesFamily and Community Medicine, Unidade de Saúde Familiar (USF) Cidade Jardim (Family Health Unit Cidade Jardim), Viseu, PRT.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Intravenous leiomyomatosis (IVL) is a rare benign smooth muscle neoplasm characterized by intravascular proliferation, often extending from the uterus to the inferior vena cava and right heart. Usually identified incidentally, IVL may present with nonspecific symptoms, including abdominal distension, weight loss, and easy bruising, particularly in women. This case report describes a 47-year-old Caucasian female who presented with progressive abdominal enlargement and other nonspecific symptoms. Imaging revealed a giant tumor occupying the abdominal and pelvic cavities, and exploratory laparotomy was proposed. The surgical intervention involved total hysterectomy and bilateral salpingo-oophorectomy, revealing IVL with extensive involvement of the uterine and para-adnexal tissues. Post-operative recovery was uneventful, and no recurrence was noted over three years of follow-up. This case highlights the importance of recognizing IVL's potential presentations and advocating for timely diagnosis and intervention. Awareness among healthcare professionals is crucial to improve outcomes in patients with this rare entity, which poses potentially severe complications.

Indexed as

clinical awarenessdiagnosisintravenous leiomyomatosisprimary healthcare servicessurgical resection

Identifiers

PMID40539160
PMCPMC12178541

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.