Concurrent Klippel-Feil Anomaly, Tethering and Dermoid Cyst Misinterpreted as Pott disease: A Case Report

Journal Title: Malaysian Orthopaedic Journal - Year 2014, Vol 8, Issue 1

Abstract

Klippel-Feil syndrome (KFS) is characterized by the failure in segmentation of two or more vertebrae due to an abnormal division of the mesodermal somites and has been reported to be associated with cardiac and central nervous system anomalies. We report a rare occurrence of concurrent Klippel-Feil anomaly, tethering and dermoid cyst of dorsal spine masquerading Potts’ disease in an eighteen years old female. In rare instances the KFS can be associated with intracranial or spinal tumors, most frequently dermoid or epidermoid cysts.

Authors and Affiliations

A Agrawal, T Gopalkrishnaiah, V Shanthi, BA Ramakrishna

Keywords

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  • EP ID EP306697
  • DOI 10.5704/MOJ.1403.002
  • Views 97
  • Downloads 0

How To Cite

A Agrawal, T Gopalkrishnaiah, V Shanthi, BA Ramakrishna (2014). Concurrent Klippel-Feil Anomaly, Tethering and Dermoid Cyst Misinterpreted as Pott disease: A Case Report. Malaysian Orthopaedic Journal, 8(1), 63-65. https://europub.co.uk./articles/-A-306697