Highlights
- •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
Background
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.
Methods
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.
Results
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”.
Conclusions
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.
Keywords
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Article info
Publication history
Published online: July 22, 2022
Accepted:
July 19,
2022
Received in revised form:
July 7,
2022
Received:
March 4,
2022
Identification
Copyright
© 2022 Elsevier B.V. All rights reserved.