AI Article Synopsis

  • A case study is presented of a man with nonketotic hyperosmolar hyperglycemia (NKHH) who developed hemichorea alongside rapid memory and cognitive decline, which is rare.
  • Imaging revealed typical striatal changes linked to NKHH-induced hemichorea, but also showcased hyperintensities and atrophy in the temporal lobe, suggesting possible transient ischemia.
  • This case highlights that NKHH may lead not only to hemichorea but also to rapid-onset dementia and temporal lobe damage, which may not completely improve even after managing blood sugar levels.

Article Abstract

Hemichorea has been well-reported in association with nonketotic hyperosmolar hyperglycemia (NKHH), but reports of concurrent temporal lobe involvement are rare. We present the case of a man with NKHH who developed hemichorea in the setting of rapidly progressive memory and cognitive impairments. He demonstrated the unilateral striatal T1 hyperintensities expected for NKHH-induced hemichorea but was also found to have fluid-attenuated inversion recovery hyperintensity, contrast enhancement, and eventual atrophy of his ipsilateral temporal lobe. A review of similar case reports and radiologic findings was performed. His temporal lobe injury shows a progression mimicking that seen in cortical laminar necrosis, suggesting transient ischemia to this lobe as a consequence of either blood hyperviscosity or vasoconstriction; atypical infections or parainfectious processes cannot fully be excluded, however. In addition to hemichorea or focal neurologic deficits, NKHH may also be associated with a rapidly progressive dementia and temporal lobe injury, with deficits that may not fully reverse after glycemic control.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7271625PMC
http://dx.doi.org/10.1177/1941874420902875DOI Listing

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