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2023, Number 1

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Rev cubana med 2023; 62 (1)

Type I Arnold-Chiari malformation with syringomyelia

Ramírez GAD, Valdés CRJ, Mendoza AJC
Full text How to cite this article

Language: Spanish
References: 13
Page: 1-7
PDF size: 311.33 Kb.


Key words:

Arnold-Chiari malformation, headache disorders, nuclear magnetic resonance.

ABSTRACT

Introduction: Arnold-Chiari malformations are a heterogeneous group of neurological disorders characterized by alterations within the regions of the cerebellum, brain stem and craniocervical junction; all result in inferior displacement of the cerebellum into the spinal canal through the foramen magnum, whether in conjunction with the inferior cord or not.
Objective: To describe the clinical findings, complementary studies, diagnostic criteria, therapeutic approach and evolution, in a case with type I Chiari malformation with syringomyelia.
Case report: A patient with an insidious course of headache is reported. She was diagnosed with type I Chiari malformation with syringomyelia, which required neurosurgical treatment. The postoperative evolution was favorable.
Conclusions: Conclusions: Arnold-Chiari malformation is a rare entity. the appearance of nuclear magnetic resonance has allowed it to be diagnosed and therefore its incidence has increased. The reported case had a classic clinical course.


REFERENCES

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  2. ASPACE. Parálisis Cerebral. Síndrome de Arnold Chiari. Segovia. 2022 Disponible en: https://aspacesegovia.com/sindrome-de-arnold-chiari/2.

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C?MO CITAR (Vancouver)

Rev cubana med. 2023;62