Evidence map›Paper›PMID 42068357›Full record

ArticleChild's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery2026

Stroke in a child with cutaneous naevi: a diagnostic trail toward suspected cavernoma-associated phakomatosis with histologic discordance and early multicentric recurrence-adjuvant therapeutic implications.

Olukorede Olabanji Adekunle, Nurudeen Abiola Adeleke, Folaranmi Oluwasegun Olaleke, Olakunle Michael Adegboye, Abdulquadri Balogun, Ehigie Joshua Ighodalo

Abstract readCase Reports
PubMed Publisher
In one paragraph

Article in Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2026. 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
–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

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

6 authors.

Olukorede Olabanji AdekunleDivision of Neurosurgery, Department of Surgery, University of Ilorin Teaching Hospital, Ilorin, Kwara State, Nigeria. adekunleolukorede@gmail.com.ORCID 0009-0002-6541-2121
Nurudeen Abiola AdelekeDivision of Neurosurgery, Department of Surgery, University of Ilorin Teaching Hospital, Ilorin, Kwara State, Nigeria.ORCID 0000-0002-7937-1730
Folaranmi Oluwasegun OlalekeDepartment of Anatomic Pathology, University of Ilorin Teaching Hospital, Ilorin, Kwara State, Nigeria.ORCID 0000-0002-0237-8934
Olakunle Michael AdegboyeDivision of Neurosurgery, Department of Surgery, University of Ilorin Teaching Hospital, Ilorin, Kwara State, Nigeria.ORCID 0000-0002-9384-4856
Abdulquadri BalogunDepartment of Anatomic Pathology, University of Ilorin Teaching Hospital, Ilorin, Kwara State, Nigeria.ORCID 0000-0001-5893-578X
Ehigie Joshua IghodaloDepartment of Anatomic Pathology, University of Ilorin Teaching Hospital, Ilorin, Kwara State, Nigeria.ORCID 0000-0002-6208-0507

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPhakomatoses, also known as neurocutaneous syndromes are rare disorders characterized by multisystem involvement with variable neurological manifestations in children, including intracranial vascular malformations. Cavernous malformations may present with acute haemorrhage and stroke-like symptoms. Diagnostic difficulty arises when radiologic findings suggest a benign lesion, yet histopathology reveals discordant malignant pathology. CASE PRESENTATION: An 8-year-old female presented with sudden-onset left hemiparesis and recurrent seizures. Physical examination revealed multiple cutaneous naevi, raising suspicion of a syndromic association. Brain magnetic resonance imaging demonstrated a well-circumscribed right parietal intra-axial lesion with a "popcorn" appearance and hypointense susceptibility blooming, highly suggestive of a cavernous malformation. Cranial computed tomography scan subsequently showed an associated large intracerebral haematoma. The patient underwent right parietal craniotomy with haematoma evacuation and excision of the lesion. The immediate postoperative course was initially satisfactory with neurological improvement. Histopathological examination of the excised specimen, however, revealed a malignant neoplasm, establishing a significant radiologic-histologic discordance which fundamentally altered the diagnostic interpretation. The patient had a relapse of symptoms two months after surgery, with repeat neuroimaging showing multicentric tumour recurrence, necessitating referral for adjuvant neuro-oncologic management.

conclusionThis case illustrates a rare diagnostic pitfall and challenge in paediatric neurosurgery, where a malignant intracranial tumour mimicked a cavernous malformation in the context of cutaneous stigmata. The report emphasizes the limitations of neuroimaging alone and underscores the importance of careful clinicoradiologic correlation, histopathological confirmation, and multidisciplinary evaluation when managing presumed vascular lesions in children, particularly in resource-limited settings.

Indexed as

Hemangioma, Cavernous, Central Nervous SystemNeurocutaneous SyndromesSkin NeoplasmsStrokeChildFemaleHumansMagnetic Resonance ImagingNeoplasm Recurrence, LocalCavernous malformationsCutaneous naeviMulticentric tumourNeurocutaneous syndromesPhakomatosesRadiologic-histologic discordance

Identifiers

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.