Advertisement
Letter to the Editor| Volume 404, P36-39, September 15, 2019

An autopsy case of MM2-thalamic subtype of sporadic Creutzfeldt-Jakob disease with Lewy bodies presenting as a sleep disorder mimicking anti-IgLON5 disease

      Highlights

      • We report a case of MM2-thalamic-sCJD presenting as a sleep disorder mimicking anti-IgLON5 disease.
      • Post-mortem analysis of brain tissue showed MM2-thalamic-sCJD with Lewy bodies (LB).
      • MM2-thalamic-sCJD with LB should be considered as a differential diagnosis of sleep disorder mimicking anti-IgLON5 disease.

      Keywords

      To read this article in full you will need to make a payment

      Purchase one-time access:

      Academic & Personal: 24 hour online accessCorporate R&D Professionals: 24 hour online access
      One-time access price info
      • For academic or personal research use, select 'Academic and Personal'
      • For corporate R&D use, select 'Corporate R&D Professionals'

      Subscribe:

      Subscribe to Journal of the Neurological Sciences
      Already a print subscriber? Claim online access
      Already an online subscriber? Sign in
      Institutional Access: Sign in to ScienceDirect

      References

        • Parchi P.
        • Giese A.
        • Capellari S.
        • Brown P.
        • Schulz-Schaeffer W.
        • Windl O.
        • et al.
        Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects.
        Ann. Neurol. 1999; 46: 224-233
        • Hamaguchi T.
        • Kitamoto T.
        • Sato T.
        • Mizusawa H.
        • Nakamura Y.
        • Noguchi M.
        • et al.
        Clinical diagnosis of MM2-type sporadic Creutzfeldt-Jakob disease.
        Neurology. 2005; 64: 643-648
        • Cortelli P.
        • Perani D.
        • Montagna P.
        • Gallassi R.
        • Tinuper P.
        • Provini F.
        • et al.
        Pre-symptomatic diagnosis in fatal familial insomnia: serial neurophysiological and 18FDG-PET studies.
        Brain. 2006; 129: 668-675
        • Sabater L.
        • Gaig C.
        • Gelpi E.
        • Bataller L.
        • Lewerenz J.
        • Torres-Vega E.
        • et al.
        A novel non-rapid-eye movement and rapid-eye-movement parasomnia with sleep breathing disorder associated with antibodies to IgLON5: a case series, characterisation of the antigen, and post-mortem study.
        Lancet Neurol. 2014; 13: 575-586
        • Gaig C.
        • Graus F.
        • Compta Y.
        • Hogl B.
        • Bataller L.
        • Bruggemann N.
        • et al.
        Clinical manifestations of the anti-IgLON5 disease.
        Neurology. 2017; 88: 1736-1743
        • Iranzo A.
        • Santamaria J.
        • Tolosa E.
        The clinical and pathophysiological relevance of REM sleep behavior disorder in neurodegenerative diseases.
        Sleep Med. Rev. 2009; 13: 385-401
        • Atarashi R.
        • Satoh K.
        • Sano K.
        • Fuse T.
        • Yamaguchi N.
        • Ishibashi D.
        • et al.
        Ultrasensitive human prion detection in cerebrospinal fluid by real-time quaking-induced conversion.
        Nat. Med. 2011; 17: 175-178
        • McKeith I.G.
        • Dickson D.W.
        • Lowe J.
        • Emre M.
        • O'Brien J.T.
        • Feldman H.
        • et al.
        Diagnosis and management of dementia with Lewy bodies: third report of the DLB consortium.
        Neurology. 2005; 65: 1863-1872
        • Abu-Rumeileh S.
        • Redaelli V.
        • Baiardi S.
        • Mackenzie G.
        • Windl O.
        • Ritchie D.L.
        • et al.
        Sporadic fatal insomnia in Europe: phenotypic features and diagnostic challenges.
        Ann. Neurol. 2018; 84: 347-360
        • Montagna P.
        • Gambetti P.
        • Cortelli P.
        • Lugaresi E.
        Familial and sporadic fatal insomnia.
        Lancet Neurol. 2003; 2: 167-176
        • Iwata S.
        • Nakamura A.
        • Nakamura N.
        • Sakashita I.
        • Fukunaga H.
        2 cases of Creutzfeldt-Jacob disease with bilateral vocal cord paralysis.
        Rinsho Shinkeigaku. 1988; 28: 333-337