The dark side of the (half) moon

Francesco Pellegrini; Altin Stafa; Daniela Bonsanto; Clare L. Fraser

doi:10.1016/j.survophthal.2019.02.001

The dark side of the (half) moon

Francesco Pellegrini^*, Altin Stafa, Daniela Bonsanto, Clare L. Fraser

^*Corresponding author for this work

Research output: Contribution to journal › Article

1 Citation (Scopus)

Abstract

A 71-year-old man was referred to neuro-ophthalmology for evaluation of reading problems associated with pituitary adenoma. Perimetry showed a right temporal crescent syndrome (“half moon” syndrome) suggesting left occipital disease. Cranial magnetic resonance imaging, electroencephalogram, and cerebrospinal fluid examination (14-3-3 protein) were consistent with a diagnosis of Creutzfeldt-Jakob disease. His neurologic condition rapidly deteriorated with memory problems, myoclonus, and apathy followed by death, 4 months later. This case shows how visual problems may be the first manifestation of this rare prion disease (Heidenhain variant of Creutzfeldt-Jakob disease).

Original language	English
Pages (from-to)	381-385
Number of pages	5
Journal	Survey of Ophthalmology
Volume	65
Issue number	3
DOIs	https://doi.org/10.1016/j.survophthal.2019.02.001
Publication status	Published - 1 May 2020
Externally published	Yes

Keywords

half moon syndrome
Heidenhain variant of Creutzfeldt-Jakob disease
temporal crescent syndrome

Access to Document

10.1016/j.survophthal.2019.02.001

Link to publication in Scopus

Fingerprint Dive into the research topics of 'The dark side of the (half) moon'. Together they form a unique fingerprint.

Cite this

Pellegrini, F., Stafa, A., Bonsanto, D., & Fraser, C. L. (2020). The dark side of the (half) moon. Survey of Ophthalmology, 65(3), 381-385. https://doi.org/10.1016/j.survophthal.2019.02.001

@article{a3a3f7cf1db54c3886bd5565a88dd06c,

title = "The dark side of the (half) moon",

abstract = "A 71-year-old man was referred to neuro-ophthalmology for evaluation of reading problems associated with pituitary adenoma. Perimetry showed a right temporal crescent syndrome (“half moon” syndrome) suggesting left occipital disease. Cranial magnetic resonance imaging, electroencephalogram, and cerebrospinal fluid examination (14-3-3 protein) were consistent with a diagnosis of Creutzfeldt-Jakob disease. His neurologic condition rapidly deteriorated with memory problems, myoclonus, and apathy followed by death, 4 months later. This case shows how visual problems may be the first manifestation of this rare prion disease (Heidenhain variant of Creutzfeldt-Jakob disease).",

keywords = "half moon syndrome, Heidenhain variant of Creutzfeldt-Jakob disease, temporal crescent syndrome",

author = "Francesco Pellegrini and Altin Stafa and Daniela Bonsanto and Fraser, {Clare L.}",

year = "2020",

month = "5",

day = "1",

doi = "10.1016/j.survophthal.2019.02.001",

language = "English",

volume = "65",

pages = "381--385",

journal = "Survey of Ophthalmology",

issn = "0039-6257",

publisher = "Elsevier",

number = "3",

}

TY - JOUR

T1 - The dark side of the (half) moon

AU - Pellegrini, Francesco

AU - Stafa, Altin

AU - Bonsanto, Daniela

AU - Fraser, Clare L.

PY - 2020/5/1

Y1 - 2020/5/1

N2 - A 71-year-old man was referred to neuro-ophthalmology for evaluation of reading problems associated with pituitary adenoma. Perimetry showed a right temporal crescent syndrome (“half moon” syndrome) suggesting left occipital disease. Cranial magnetic resonance imaging, electroencephalogram, and cerebrospinal fluid examination (14-3-3 protein) were consistent with a diagnosis of Creutzfeldt-Jakob disease. His neurologic condition rapidly deteriorated with memory problems, myoclonus, and apathy followed by death, 4 months later. This case shows how visual problems may be the first manifestation of this rare prion disease (Heidenhain variant of Creutzfeldt-Jakob disease).

AB - A 71-year-old man was referred to neuro-ophthalmology for evaluation of reading problems associated with pituitary adenoma. Perimetry showed a right temporal crescent syndrome (“half moon” syndrome) suggesting left occipital disease. Cranial magnetic resonance imaging, electroencephalogram, and cerebrospinal fluid examination (14-3-3 protein) were consistent with a diagnosis of Creutzfeldt-Jakob disease. His neurologic condition rapidly deteriorated with memory problems, myoclonus, and apathy followed by death, 4 months later. This case shows how visual problems may be the first manifestation of this rare prion disease (Heidenhain variant of Creutzfeldt-Jakob disease).

KW - half moon syndrome

KW - Heidenhain variant of Creutzfeldt-Jakob disease

KW - temporal crescent syndrome

UR - http://www.scopus.com/inward/record.url?scp=85065033905&partnerID=8YFLogxK

U2 - 10.1016/j.survophthal.2019.02.001

DO - 10.1016/j.survophthal.2019.02.001

M3 - Article

VL - 65

SP - 381

EP - 385

JO - Survey of Ophthalmology

JF - Survey of Ophthalmology

SN - 0039-6257

IS - 3

ER -