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Idiopathic intracranial hypertension occurred after spinal surgery: report of two rare cases and systematic review of the literature

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Abstract

Background

Idiopathic intracranial hypertension (IIH) is a relatively rare syndrome of increased intracranial pressure of unknown etiology. It is characterized by cerebrospinal fluid (CSF) opening pressure more than 250 mmH2O, with normal cranial imaging and CSF content. IIH occurred after spinal surgery is extremely rare.

Methods

We present two IIH cases occurred after spinal surgery and conduct a systematic review of articles reporting IIH occurred after spinal surgery.

Results

The first patient underwent a posterior decompression and fixation for cervical fractures. IIH symptoms appeared 3 days postoperatively and gradually resolved with appropriate medication. The second patient underwent posterior spinal fusion with segmental instrumentation for congenital scoliosis. IIH symptoms appeared 5 days postoperatively and the patient died due to the irreversible intracranial hypertension although underwent intensive care and treatment. The literature review revealed that there were only five cases of IIH occurred after spinal surgery reported till date.

Conclusions

IIH occurred after spinal surgery is relatively rare; the diagnosis is based upon exclusion of other diseases. IIH should be kept in mind in patients underwent spinal surgery as it could develop into irreversible intracranial hypertension.

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Acknowledgments

This work was supported by the Grants from the National Nature Science Foundation of China (Nos. 81171756 and 81501908) and the Nature Science Foundation of Zhejiang Province (LY14H60004).

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Correspondence to Qixin Chen.

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None of the authors has any potential conflict of interest.

Additional information

Z. Xu and H. Li contributed equally to this work.

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Xu, Z., Li, H., Chen, G. et al. Idiopathic intracranial hypertension occurred after spinal surgery: report of two rare cases and systematic review of the literature. Eur Spine J 26 (Suppl 1), 9–16 (2017). https://doi.org/10.1007/s00586-016-4578-1

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  • DOI: https://doi.org/10.1007/s00586-016-4578-1

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