Evidence map›Paper›PMID 37228362›Full record

ArticleJAAD international2023

Lymphatic differentiation and microvascular proliferation in benign vascular lesions of skin and soft tissue: Diagnostic features following the International Society for The Study of Vascular Anomalies Classification-A retrospective study.

Amalia Mulia Utami, Max M Lokhorst, Lorine B Meijer-Jorna, Mara A Kruijt, Sophie E R Horbach, Onno J de Boer, Chantal M A M van der Horst, Allard C van der Wal

Open access · goldAbstract read
In one paragraph

Article in JAAD international, 2023. 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
0cells of the map it votes in
0citing papers in PubMed
1.3field-weighted citation impact, top 21% of its field
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

0 citing papers in PubMed, 4 citations in OpenAlex.

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

8 authors at 2 institutions in 2 countries.

Amalia Mulia UtamiDepartment of Pathology, Amsterdam University Medical Center-Location Academic Medical Center (AMC), University of Amsterdam, Amsterdam, The Netherlands.
Max M LokhorstDepartment of Plastic Surgery, Amsterdam University Medical Center-Location Academic Medical Center (AMC), University of Amsterdam, Amsterdam, The Netherlands.
Lorine B Meijer-JornaSymbiant Pathology, Noord-west Ziekenhuis (NWZ)- Noordwest Ziekenhuisgroep, Alkmaar, The Netherlands.
Mara A KruijtDepartment of Pathology, Amsterdam University Medical Center-Location Academic Medical Center (AMC), University of Amsterdam, Amsterdam, The Netherlands.
Sophie E R HorbachDepartment of Plastic Surgery, Amsterdam University Medical Center-Location Academic Medical Center (AMC), University of Amsterdam, Amsterdam, The Netherlands.
Onno J de BoerDepartment of Pathology, Amsterdam University Medical Center-Location Academic Medical Center (AMC), University of Amsterdam, Amsterdam, The Netherlands.
Chantal M A M van der HorstDepartment of Plastic Surgery, Amsterdam University Medical Center-Location Academic Medical Center (AMC), University of Amsterdam, Amsterdam, The Netherlands.
Allard C van der WalDepartment of Pathology, Amsterdam University Medical Center-Location Academic Medical Center (AMC), University of Amsterdam, Amsterdam, The Netherlands.
Amsterdam UMC Location University of Amsterdam · NLNoordwest Ziekenhuisgroep · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Discrepancies have been noted between the clinical and histologic diagnosis of vascular malformations. Objective: To evaluate the effectiveness of the International Society for Study of Vascular Anomalies (ISSVA) classification in diagnosing benign vascular anomalies based on clinical and (immuno) histologic parameters, focusing on lymphatic differentiation and vascular proliferation. Method: A retrospective study of 121 consecutive patients with benign skin and soft-tissue vascular anomalies located in the head and neck region (pyogenic granulomas and angioma senilis were excluded) by applying multiplex immunohistochemistry staining for lymph vessels (D2-40), endothelial blood vessels, and proliferating cells (Ki67). Clinical and histologic diagnosis was revised after the ISSVA classification. Results: Initially, 64 lesions were diagnosed as tumors and 57 as malformations. Revision diagnosis following the ISSVA classification revealed 27 tumors, 90 malformations (22.2% lymphatic), and 4 non-ISSVA. Immunostaining showed lymphatic differentiation in 24 (19.8%) of 121 cases, of which 20 were malformations. Proliferative activity (Ki67+) was found in 41 (33.8%) of 121 cases, of which 8 were arteriovenous malformations. Limitation: Quality and size of materials (biopsies vs resections) and clinical information. Conclusion: The diagnostic accuracy of combined histologic and clinical approaches for identifying vascular anomalies following the ISSVA classification can be substantially enhanced by incorporating additional immunostaining techniques to evaluate lymphatic differentiation and proliferative activity, particularly in identifying the occurrence of vascular malformations.

Indexed as

ISSVA classificationlymphatic vesselsmicrovascular proliferationskin tumorsoft-tissue tumorvascular anomaliesvascular malformations

Identifiers

PMID37228362
PMCPMC10203759
OpenAlexW4362659006

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.