Evidence map›Paper›PMID 39139758›Full record

ArticleJournal of surgical case reports2024

Massive cellular angiofibroma of the vulva: a case report.

Hounaida Mahfoud, Ibtissam Bensrhir, Meryem Abbouch, Chourouq Mustapha Eid, Mariame Meziane, Samia Sassi, Najat Lamalmi, Najia Zeraidi, Aziz Baidada

Abstract readCase Reports
In one paragraph

Article in Journal of surgical case reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
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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

9 authors.

Hounaida MahfoudGynaecology-Obstetrics and Endoscopy Department, Maternity Souissi, University Hospital Center IBN SINA, University Mohammed V, Rabat 10100, Morocco.ORCID https://orcid.org/0000-0002-8156-3176
Ibtissam BensrhirGynaecology-Obstetrics and Endoscopy Department, Maternity Souissi, University Hospital Center IBN SINA, University Mohammed V, Rabat 10100, Morocco.
Meryem AbbouchGynaecology-Obstetrics and Endoscopy Department, Maternity Souissi, University Hospital Center IBN SINA, University Mohammed V, Rabat 10100, Morocco.
Chourouq Mustapha EidDepartment of Dermatology, University Hospital Center IBN SINA, University Mohammed V, Rabat 10100, Morocco.
Mariame MezianeDepartment of Dermatology, University Hospital Center IBN SINA, University Mohammed V, Rabat 10100, Morocco.
Samia SassiDepartment of Pathology, University Hospital Center IBN SINA, University Mohammed V, Rabat 10100, Morocco.
Najat LamalmiDepartment of Pathology, University Hospital Center IBN SINA, University Mohammed V, Rabat 10100, Morocco.
Najia ZeraidiGynaecology-Obstetrics and Endoscopy Department, Maternity Souissi, University Hospital Center IBN SINA, University Mohammed V, Rabat 10100, Morocco.
Aziz BaidadaGynaecology-Obstetrics and Endoscopy Department, Maternity Souissi, University Hospital Center IBN SINA, University Mohammed V, Rabat 10100, Morocco.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cellular angiofibroma is a rare benign mesenchymal tumor, typically occurring in the vulvar region of middle-aged women. This report highlights the importance of histological analysis in diagnosing this uncommon condition and emphasizes its benign nature and straightforward management. We present a case of a 58-year-old North African woman who had a large, well-defined mass in the left labia majora, which had been evolving over 2 years. MRI confirmed the resectability of the tumor by delineating its boundaries. The tumor, despite its slow growth leading to delayed diagnosis, was effectively treated with wide surgical excision. Diagnosis was confirmed through histological and immunohistochemical evaluations, revealing spindle cell proliferation with thick-walled vessels. Cellular angiofibroma, although initially alarming due to its size, is generally managed successfully with surgery and prognosis is favorable with a low risk of recurrence.

Indexed as

cellular angiofibromaimmunochemistrylarge excisionmesenchymal tumorvulvar mass

Identifiers

PMID39139758
PMCPMC11321720

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