Evidence map›Paper›PMID 40656466›Full record

ArticleSurgical neurology international2025

Chiari I malformation with syringomyelia: Exploring novel dermatological markers in pediatrics.

Soumi Kundu, Pradosh Kumar Sarangi, Firdaus Bano, Sarthak Das, Saroj Kumar Tripathy

Abstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Surgical neurology international, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

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No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Soumi KunduDepartment of Pediatrics, All India Institute of Medical Sciences, Deoghar, Jharkhand, India.
Pradosh Kumar SarangiDepartment of Radiodiagnosis, All India Institute of Medical Sciences, Deoghar, Jharkhand, India.
Firdaus BanoDepartment of Pediatrics, All India Institute of Medical Sciences, Deoghar, Jharkhand, India.
Sarthak DasDepartment of Pediatrics, All India Institute of Medical Sciences, Deoghar, Jharkhand, India.
Saroj Kumar TripathyDepartment of Pediatrics, All India Institute of Medical Sciences, Deoghar, Jharkhand, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Chiari I malformation (CM1) and syringomyelia can present a wide spectrum of symptoms and signs in children, often varying with age. However, the association of CM1 with dermatographia and alopecia is exceedingly rare and, to our knowledge, has not been previously reported in the pediatric population. Case Description: We present the case of a 7-year-old boy who exhibited an unusual constellation of findings, including Horner's syndrome, dermatographia, and patchy alopecia. Magnetic resonance imaging revealed CM1 with holocord syringomyelia. Conclusion: This case highlights the importance of considering CM1 in the differential diagnosis of pediatric patients with unexplained dermatological and neurological findings. Early diagnosis and a multidisciplinary approach are crucial to achieving favorable outcomes.

Indexed as

AlopeciaChiari I malformationDermatological markersPediatricsSyringomyelia

Identifiers

PMID40656466
PMCPMC12255215

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