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Transient global amnesia with unexpected clinical and radiological findings: A case series and systematic review.

Authors :
Piffer, Silvio
Nannoni, Stefania
Maulucci, Francesco
Beaud, Valérie
Rouaud, Olivier
Förster, Alex
Cereda, Carlo W.
Maeder, Philippe
Michel, Patrik
Source :
Journal of the Neurological Sciences. Oct2022, Vol. 441, pN.PAG-N.PAG. 1p.
Publication Year :
2022

Abstract

Transient global amnesia (TGA) represents a benign neurological syndrome of unknown pathophysiology, often accompanied by vanishing hippocampal punctate diffusion-weighted imaging lesions (HPDL). The literature suggests that TGA may present with unusual features. This study analyses atypical clinical and radiological manifestations of patients with TGA and/or HPDL. We retrospectively reviewed patients with atypical clinical or radiological presentations of TGA and/or HPDL in three neurology centers. We also performed a systematic review of literature using predefined search terms. Results were classified as: A) Atypical clinical manifestations of TGA (such as amnesia with additional manifestations, or only non-amnesic manifestations); B) Atypical radiological manifestations of clinically typical TGA. We identified 83 patients: 18 in our centres (median age 63.5 years, 39% female) and 65 in the literature. In group A, 43 patients presented atypical clinical manifestations such as TGA with added transitory cognitive or sensory-motor deficits, seizures, headaches, but also non-amnesic presentations associated with HPDL and incidental HPDL without symptoms. In group B, 40 patients with typical clinical TGA showed extra-hippocampal punctate diffusion lesions (E -HPDL) which disappeared on follow-up imaging. Using clinical and radiological manifestations, we classified these patients into different categories describing a "TGA-PDL spectrum". TGA may have atypical clinical manifestations despite typical neuroimaging and patients with typical TGA may show vanishing extra-hippocampal punctate diffusion lesions. TGA, related clinical manifestations, and vanishing punctate diffusion lesions should be considered part of a larger "TGA-PDL spectrum", allowing for better diagnosis of typical and atypical cases and stimulating further studies. • TGA may occasionally be accompanied by clinical features outside the strict original definition. • In addition to the characteristic HPDL, extra-hippocampal punctate vanishing lesions may be seen in TGA. • We propose a the term "TGA-HPDL spectrum", allowing classification also of atypical clinical and radiological cases. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
0022510X
Volume :
441
Database :
Academic Search Index
Journal :
Journal of the Neurological Sciences
Publication Type :
Academic Journal
Accession number :
159188227
Full Text :
https://doi.org/10.1016/j.jns.2022.120349