Journal
JOURNAL OF THE NEUROLOGICAL SCIENCES
Volume 441, Issue -, Pages -Publisher
ELSEVIER
DOI: 10.1016/j.jns.2022.120349
Keywords
Transient global amnesia; Hippocampal punctate diffusion lesion; Atypical transient global amnesia; Amnesia; Magnetic resonance imaging
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This study analyzed the atypical clinical and radiological manifestations of patients with transient global amnesia (TGA) and/or hippocampal punctate diffusion-weighted imaging lesions (HPDL). The results showed that TGA may have atypical clinical manifestations, and patients with typical TGA may show disappearing extra-hippocampal punctate diffusion lesions. These findings contribute to better diagnosis of typical and atypical cases and stimulate further research.
Background: Transient global amnesia (TGA) represents a benign neurological syndrome of unknown patho-physiology, 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 manifes-tations, 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.
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