Annals of Movement Disorders (Jan 2020)

Steroid responsive catatonia: A case of Hashimoto’s encephalopathy

  • Ritu Shree,
  • Govind Madhaw,
  • Rajat Manchanda,
  • Divya M Radhakrishnan,
  • Niraj Kumar

DOI
https://doi.org/10.4103/AOMD.AOMD_32_19
Journal volume & issue
Vol. 3, no. 1
pp. 51 – 55

Abstract

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Hashimoto’s encephalopathy (HE) commonly presents with two types of neurological presentation: recurrent stroke-like episodes or seizures and progressive cognitive decline. Being a treatable disorder, one cannot afford to miss the diagnosis. We report a female with HE who presented with a history of recurrent episodes of catatonia, recovering completely with steroids. The diagnosis of the primary disease got delayed for 5 months. HE presenting as catatonia has been reported rarely. A high degree of suspicion in appropriate clinical settings, resulting in early diagnosis, is rewarding as HE usually show good response to corticosteroids.

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