Altered ioflupane single‐photon emission computed tomography in anti‐IgLON5 disease: A new case mimicking probable progressive supranuclear palsy and review of the literature. (2nd December 2020)

• Record Type: Journal Article
• Authors: González‐Ávila, Carmen; Casado, Laura; Muro García, Inés; Villacieros‐Álvarez, Javier; Vivancos, José; Quintas, Sonia
• Is Part Of: European journal of neurology. Volume 28:Number 4(2021)
• Page Start: 1392
• Page End: 1395
• Publication Date: 2020-12-02
• Subjects: anti‐IgLON5 disease -- ioflupane SPECT -- parkinsonism -- progressive supranuclear palsy -- tauopathy; Neurology -- Periodicals; Nervous system -- Diseases -- Periodicals; 616.8
• DOI: 10.1111/ene.14634
• Languages: English
• ISSNs: 1351-5101

Abstract

Abstract: Background and purpose: Anti‐IgLON5 disease is a rare disorder characterized by a heterogeneous myriad of symptoms that may include sleep disorders, bulbar dysfunction, gait problems, movement disorders, cognitive impairment, oculomotor abnormalities, and nervous system hyperexcitability. Its physiopathology remains unknown, with a combination of both autoimmune and neurodegenerative findings. Methods: We describe clinical, cerebrospinal fluid (CSF), and ioflupane single‐photon emission computed tomography (SPECT) findings of a positive case of anti‐IgLON5 disease mimicking probable progressive supranuclear palsy (PSP). We performed a literature review of previous publications reporting on anti‐IgLON5 disease and ioflupane SPECT. Results: We report the case of a 66‐year‐old male who met clinical criteria for probable PSP, in whom ioflupane SPECT showed an alteration of the left presynaptic dopaminergic pathway. However, the presence of atypical neurological symptoms for PSP led to further complementary tests, and IgLON5 antibodies were detected in CSF. According to our literature review, ioflupane SPECT findings have been previously described in only three other patients with anti‐IgLON5 disease, with a reduced uptake in the striatum in two of them. Conclusions: Ioflupane SPECT abnormalities, though scarcely described, are not uncommon in anti‐IgLON5 disease. They could be related to nigrostriatal dopaminergic degeneration in the context of the tauopathy component of the disease, but further case descriptions are necessary. Abstract : Anti‐IgLON5 disease can mimic progressive supranuclear palsy (PSP). An altered DATSCAN can be observed in patients with anti‐IgLON5 disease. The physiopathology of this disease includes autoimmune and tauopathy findings.