Skip to main content
Log in

Thoracolumbar Arachnoid Cyst with Horner Syndrome: A Case Report and Review of the Literature

  • Original Paper
  • Published:
Cell Biochemistry and Biophysics Aims and scope Submit manuscript

Abstract

Horner syndrome (HS) results from the interruption of sympathic pathway, and the patients have a group of signs including miosis, ptosis, enophthalmos, and anhydrosis. While HS is mainly caused by cervical sympathetic nerve injury such as sympathetic chain tumor, we report here a HS case caused by a thoracolumbar arachnoid cyst. Imageological examination showed the cyst existed in spinal canal from the T11 to L3 level, which was further confirmed by operation. The tumor attacked the lateral margin of intervertebral foramen at certain stages. In MRI scan, no abnormality was found in the patient’s crania, cervical vertebra, thoracic vertebra, or the other parts. After removal of the cyst with operation, the patient’s HS symptoms and weakness of lower limbs were relieved apparently. Although the sympathetic center origins from the cornu laterale medullae spinalis of T1 to L3, there are many reports about HS caused by lumbar anesthesia and epidural anesthesia according to our literature review, and there is no report about HS results from intraspinal space-occupying lesion below T11 level. Our finding suggests that when the sympathetic center below the level of T11 emits nerve to dominate abdominal viscera, it can also control the sweat glands from face to feet, including pupils and eyelids. When physicians encounter patients with HS and one side of the body and abdominal viscera sympathetic syndromes, the pathological changes in lower thoracic vertebra or lumbar vertebra should be taken in consideration.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5

Similar content being viewed by others

References

  1. Pirouzian, A., Holz, H. A., Ip, K. C., & Sudesh, R. (2010). Acquired infantile Horner syndrome and spontaneous internal carotid artery dissection: A case report and review of literature. Journal of AAPOS : The Official Publication of the American Association for Pediatric Ophthalmology and Strabismus/American Association for Pediatric Ophthalmology and Strabismus, 14, 172–174.

    Article  Google Scholar 

  2. Syed, M. I., Baring, D., Addidle, M., Murray, C., & Adams, C. (2007). Lemierre syndrome: Two cases and a review. The Laryngoscope, 117, 1605–1610.

    Article  PubMed  Google Scholar 

  3. Kepes, E. R., Stark, D., Pantuck, E., et al. (1972). Horner’s syndrome following caudal anesthesia. New York State Journal of Medicine, 72, 946–947.

    Google Scholar 

  4. Clayton, K. C. (1983). The incidence of Horner’s syndrome during lumbar extradural for elective Caesarean section and provision of analgesia during labour. Anaesthesia, 38, 583–585.

    CAS  PubMed  Google Scholar 

  5. Mohan, J., & Potter, J. M. (1975). Pupillary constriction and ptosis following caudal epidural analgesia. Anaesthesia, 30, 769–773.

    Article  CAS  PubMed  Google Scholar 

  6. Mohan, J., Lloyd, J. W., & Potter, J. M. (1973). Pupillary constriction following extradural analgesia. Injury, 5, 151–152.

    Article  CAS  PubMed  Google Scholar 

  7. Westermaier, T., Schweitzer, T., & Ernestus, R. I. (2012). Arachnoid cysts. Advances in Experimental Medicine and Biology, 724, 37–50.

    CAS  PubMed  Google Scholar 

  8. Inagaki, T. (2011). Congenital anomalies in the central nervous system (12) arachnoid cyst. No shinkei geka. Neurological Surgery, 39, 1105–1111.

    PubMed  Google Scholar 

  9. Greenberg, M. S., & Arredondo, N. (2006). Handbook of neurosurgery (6th ed.). Lakeland, FL, New York: Greenberg Graphics; Thieme Medical Publishers.

    Google Scholar 

  10. Fridman, A. (2004). Reversible Horner syndrome caused by solitary plasmacytoma of second thoracic vertebrae. Leukaemia & Lymphoma, 45(12), 2531–2532.

    Article  CAS  Google Scholar 

Download references

Acknowledgments

This work was supported by National Natural Science Foundation of China (Grant Nos. 81372869 and 81172555 to Y.G., Z.H., A.J., H.Z., and H.L.) and National Natural Science Fundation of Guangdong Province (Grant No. S2013010016052 to R.Z. and H.L.).

Author information

Authors and Affiliations

Authors

Corresponding authors

Correspondence to Renshi Zhou or Hai Lu.

Additional information

Yang Gao and Hui Zhang contributed equally as first authors.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Gao, Y., Zhang, H., Yang, J. et al. Thoracolumbar Arachnoid Cyst with Horner Syndrome: A Case Report and Review of the Literature. Cell Biochem Biophys 71, 1293–1297 (2015). https://doi.org/10.1007/s12013-014-0347-0

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s12013-014-0347-0

Keywords

Navigation