Russian Medical Inquiry
(RMZh. Meditsinskoe Obozrenie) ISSN 2587-6821 (Print), 2686-9918 (Online)

Surgery for Arnold–Chiari malformation associated with persistent atrial fibrillation: case history

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I.M. Gilemkhanova1,2, Sh.M. Safin1,2, Kh.P. Derevyanko1

1Bashkir State Medical University, Ufa

2Republican Children’s Clinical Hospital, Ufa

Arnold–Chiari malformation is a group of congenital malformations of the posterior encephalon affecting structural relations between cerebellum, brainstem, upper cervical spinal cord, and bones of the skull base. Sporadic published data on Arnold–Chiari malformation associated with cardiac rhythm disturbances are available. This paper describes authors’ case history of Arnold–Chiari malformation associated with syringomyelia, retrocerebellar cyst, and tachyarrhythmia uncontrollable by medications in a 49-year-old woman. The woman was observed by therapist and cardiologist for abnormal heart rhythm (disease duration 6 years). She was presented with novel complaints of temporary loss of consciousness, dizziness, and abnormal coordination which required additional neurological diagnostics. After neurosurgery, cardiac rhythm has restored, neurological signs have regressed.

This case history demonstrates that Arnold–Chiari malformation can result in abnormal  heart rhythm. Clinically, craniovertebral junction disorders should be excluded in patients with cardiac arrhythmias uncontrollable by medications in association with neurological signs. Early management of craniovertebral junction disorders provides complete resolution of cardiac disorder.

Keywords: Arnold–Chiari malformation, syringomyelia, retrocerebellar cyst, cardiac rhythm disorders.

For citation: Gilemkhanova I.M., Safin Sh.M., Derevyanko Kh.P. Surgery for Arnold–Chiari malformation associated with persistent atrial fibrillation: case history. RMJ. Medical Review. 2019;11(I):31–33.



Клинический случай хирургического лечения аномалии Арнольда — Киари с персистирующей фибрилляцией предсердий
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