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Heidenhain variant of Creutzfeldt-Jakob disease masquerading as neuromyelitis optica spectrum disorder: recognizing when apheresis is not the answer

Title: Heidenhain variant of Creutzfeldt-Jakob disease masquerading as neuromyelitis optica spectrum disorder: recognizing when apheresis is not the answer
Authors: Burke, Olivia; Jacobs, Jeremy W; Tormey, Christopher A; Rinder, Henry M; Figueroa Villalba, Cristina A; Lee, Edward S; Silva Campos, Juan J; Abels, Elizabeth; Yurtsever, Nalan
Source: Laboratory Medicine ; volume 55, issue 4, page 520-523 ; ISSN 0007-5027 1943-7730
Publisher Information: Oxford University Press (OUP)
Publication Year: 2023
Description: The Heidenhain variant of Creutzfeld-Jakob disease (CJD) is a rare form that initially presents with visual disturbances. In early stages, the presentation can mimic neuromyelitis optica spectrum disorders (NMOSD) and lead to unnecessary treatment modalities. Herein, we describe a case of a 66-year-old man who presented with bilateral vision loss and retro-orbital discomfort. In addition to immunosuppressive therapy, he received 4 rounds of therapeutic plasma exchange after his preliminary diagnosis of NMOSD. We were surprised to note that his condition did not show improvement but deteriorated, with severe neurocognitive symptoms. Eventually, CJD was suspected, and real-time quaking-induced conversion (RT-QuIC) was performed. By the time the diagnosis of Heidenhain variant of CJD was confirmed, the patient was discharged to hospice care and died shortly after.
Document Type: article in journal/newspaper
Language: English
DOI: 10.1093/labmed/lmad107
Availability: https://doi.org/10.1093/labmed/lmad107; https://academic.oup.com/labmed/article-pdf/55/4/520/58391860/lmad107.pdf
Rights: https://academic.oup.com/pages/standard-publication-reuse-rights
Accession Number: edsbas.D24A3DC6
Database: BASE