Evidence map›Paper›PMID 39712813›Full record

ArticleCureus2024

Successful Treatment of Low-Flow Vascular Malformation in the Lip Using Intralesional Bleomycin: A Case Report.

Anudeep Gopishetty, K Amarnath, D P Uma Magesh, G Saichand

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In one paragraph

Article in Cureus, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
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0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Anudeep GopishettyDepartment of Oral and Maxillofacial Surgery, Meghna Institute of Dental Sciences, Nizamabad, IND.
K AmarnathDepartment of Oral and Maxillofacial Surgery, Meghna Institute of Dental Sciences, Nizamabad, IND.
D P Uma MageshDepartment of Oral and Maxillofacial Surgery, Sri Venkateshwara Dental College, Chennai, IND.
G SaichandDepartment of Oral and Maxillofacial Surgery, Meghna Institute of Dental Sciences, Nizamabad, IND.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Vascular malformations (VMs) are congenital abnormalities of blood or lymphatic vessels, present at birth and growing proportionally with the individual. They are classified into types such as capillary, venous, lymphatic, and arteriovenous malformation (AVMs). Symptoms include discoloration, swelling, pain, or functional impairment, depending on the type and location. Diagnosis involves imaging like ultrasound, MRI, or angiography, and treatment options include sclerotherapy, laser therapy, embolization, or surgery for symptomatic cases. It is a class of vascular anomalies, known as VMs are benign lesions that arise from aberrant vascular tissue and can result from either lymphatic proliferation or angiovascular dysregulation. High-flow VMs, such as AVMs, involve direct connections between arteries and veins. AVMs can be congenital, presenting at birth. They are typically persistent and progressive, with the potential to cause significant blood loss, which can be life-threatening. Several treatment modalities are available, including surgical excision, electrocautery, LASER therapy, cryotherapy, radiotherapy, and the use of locally injected agents. Among these, sclerosing agents are particularly advantageous due to their affordability, availability, and high efficacy. Commonly used sclerosing agents include ethanol, sodium morrhuate, sodium tetradecyl sulfate (STS), boiling contrast media, and bleomycin. This case report describes a VM with low-flow characteristics located at the commissure of the lip, which was successfully treated with intralesional bleomycin injections. The aim of this case report is to document the successful management of a low-flow VM at the lip commissure using intralesional bleomycin injections. It highlights the efficacy and safety of this minimally invasive treatment in achieving favorable cosmetic and functional outcomes. The study also seeks to contribute to the growing evidence supporting sclerotherapy as a reliable alternative to surgical intervention.

Indexed as

intralesional bleomycinlow-flow lesionoral surgerysclerotherapyvascular malformation

Identifiers

PMID39712813
PMCPMC11662149

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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.