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 › peer-review

2 Citations (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

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10.1016/j.survophthal.2019.02.001

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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).",

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AU - Pellegrini, Francesco

AU - Stafa, Altin

AU - Bonsanto, Daniela

AU - Fraser, Clare L.

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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

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SN - 0039-6257

VL - 65

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JO - Survey of Ophthalmology

JF - Survey of Ophthalmology

IS - 3

ER -

The dark side of the (half) moon

Abstract

Keywords

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