Evidence map›Paper›PMID 37865964›Full record

ReviewChild's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery2024

Large aplasia cutis congenita of the vertex conservative management.

Sofiene Bouali, Sarah Houimli Charfeddine, Khalil Ghedira, Haifa Mechergui, Khansa Abderrahmen, Jalel Kallel

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PubMed Publisher
In one paragraph

Review in Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 19% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 7 citations in OpenAlex.

  1. Aplasia cutis congenita of the scalp with skull defect: an individual patient data systematic review of clinical features and treatment approaches.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2026
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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

6 authors at 2 institutions in 1 country.

Sofiene BoualiDepartment of Neurosurgery, National Institute of Neurology"Mongi Ben Hmida", Tunis Faculty of Medicine, University of Tunis El Manar, Tunis, Tunisia. sofienebouali@hotmail.fr.
Sarah Houimli CharfeddineReconstructive & Aesthetic Surgery Department, Trauma & Burns Center, Ben Arous, Tunisia.
Khalil GhediraDepartment of Neurosurgery, National Institute of Neurology"Mongi Ben Hmida", Tunis Faculty of Medicine, University of Tunis El Manar, Tunis, Tunisia.
Haifa MecherguiDepartment of Neurosurgery, National Institute of Neurology"Mongi Ben Hmida", Tunis Faculty of Medicine, University of Tunis El Manar, Tunis, Tunisia.
Khansa AbderrahmenDepartment of Neurosurgery, National Institute of Neurology"Mongi Ben Hmida", Tunis Faculty of Medicine, University of Tunis El Manar, Tunis, Tunisia.
Jalel KallelDepartment of Neurosurgery, National Institute of Neurology"Mongi Ben Hmida", Tunis Faculty of Medicine, University of Tunis El Manar, Tunis, Tunisia.
Tunis El Manar University · TNCompagnie Africaine des Peintures · TN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAplasia cutis congenita (ACC) of the vertex with bone defect is a rare and begnin anomaly that can involve the epidermis, dermis, and subcutaneous tissues of the scalp with significant bone defect Bajpai and Pal (J Pediatr Surg 38(2):e4, 2003). When associated with skull defect, this rare malformation carries the risk of severe complications such as rupture of the superior sagittal sinus or infections. METHODS AND

resultsWe report a case of aplasia cutis congenita of the scalp with skull defect measuring 9 × 10 cm and an exposed sagittal sinus in a newborn. Both conservative and surgical methods have been proposed to treat this condition. In our case, conservative treatment was planned led to complete epithelization and the patient was healing well at 5 years of follow-up.

conclusionsACC of the vertex with a large scalp defects present a management dilemma Rocha et al. (Clin Case Rep 3(10):841-4, 2015). Based on a review of the literature, we report this case to demonstrate that even for the largest skin and bone defects, an initial conservative approach may allow for complete wound closure without the need for early surgical intervention.

Indexed as

Conservative TreatmentEctodermal DysplasiaHumansInfant, NewbornScalpSkinAcutis dermal dysplasiaBone defectConservative treatmentScalp defects

Identifiers

PMID37865964
OpenAlexW4387860837

What OpenQuestion holds

Textmetadata
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.