Evidence map›Paper›PMID 39286662›Full record

ArticleClinical, cosmetic and investigational dentistry2024

Surgical Management of Hereditary Gingival Fibromatosis: Case Series.

Hassina Shadab, Aisha Nawabi, Abdurrahman Anwari, Mohammad Bashir Nejabi, Elaha Somaya Ghafari, Sajeya Karimi, Mohammad Eissa Ahmadi

Abstract readCase Reports
In one paragraph

Article in Clinical, cosmetic and investigational dentistry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

7 authors.

Hassina ShadabPeriodontics Department, Kabul University of Medical Sciences (KUMS), Kabul, Afghanistan.
Aisha NawabiPeriodontics Department, Kabul University of Medical Sciences (KUMS), Kabul, Afghanistan.
Abdurrahman AnwariOperative/ Restorative Dentistry and Endodontics Department, Kabul University of Medical Sciences (KUMS), Kabul, Afghanistan.ORCID 0000-0002-6347-3353
Mohammad Bashir NejabiProsthodontics Department, Kabul University of Medical Sciences (KUMS), Kabul, Afghanistan.
Elaha Somaya GhafariPeriodontics Department, Kabul University of Medical Sciences (KUMS), Kabul, Afghanistan.ORCID 0000-0001-9305-809X
Sajeya KarimiPeriodontics Department, Kabul University of Medical Sciences (KUMS), Kabul, Afghanistan.
Mohammad Eissa AhmadiPeriodontics Department, Kabul University of Medical Sciences (KUMS), Kabul, Afghanistan.ORCID 0009-0005-3458-5304

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hereditary gingival fibromatosis (HGF) is an uncommon genetic condition marked by gradual and progressive overgrowth of fibrous tissue in the gums, which is benign in nature. It is a genetic disorder inherited in an autosomal dominant pattern, known for its considerable genetic diversity. The marginal, attached, and interdental gingivae are affected by this condition. The affected area appears pink, does not bleed easily, and exhibits a firm, fibrotic texture. Additionally, it displays a hard, widespread nodular growth that is smooth to stippled and has little bleeding tendency. Nevertheless, in certain instances, the enlargement may feel so dense and firm that it resembles bone upon palpation. Accordingly, esthetics and functions related to a healthy gingiva is also affected. The choice of treatment modality often depends on factors such as the severity of gingival overgrowth, available resources, and patient-specific considerations. Laser techniques and electrosurgery have emerged as valuable options, providing benefits like reduced discomfort and enhanced precision. However, traditional surgical methods remain highly effective, particularly when advanced technologies are not available. This article reports on three cases of hereditary gingival fibromatosis (HGF) treated with conventional gingivectomy, flap procedures, and resective osseous surgery (osteoplasty and osteotomy). The aim is to support the efficacy of these interventions in addressing patient complaints and preparing the groundwork for managing additional issues, such as speech and mastication difficulties, delayed eruption of permanent teeth, and malocclusion. The surgical treatment led to significant improvements: masticatory function was markedly enhanced, aesthetic outcomes were notably better, and oral hygiene significantly improved. Additionally, the procedures created favorable conditions for future treatments, including orthodontics, implants, or prosthetics, by providing a more manageable and functional oral environment.

Indexed as

case seriesgingival enlargementgingivectomyhereditary gingival fibromatosisosteoplasty

Identifiers

PMID39286662
PMCPMC11403129

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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.