Temporal lobe epilepsy with isolated amygdala enlargement: anatomo-electro-clinical features and long-term outcome.

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Tác giả: Margherita Bevilacqua, Dalila Biancheri, Valeria Cuccarini, Marco de Curtis, Angelo Del Sole, Francesco Deleo, Roberta Di Giacomo, Giuseppe Didato, Fabio Martino Doniselli, Rosalba Ferrario, Margarida Ferro, Rita Garbelli, Gianluca Marucci, Annalisa Parente, Chiara Pastori, Rui Quintas, João Nuno Ramos, Michele Rizzi, Andrea Stabile, Flavio Villani, Elisa Visani

Ngôn ngữ: eng

Ký hiệu phân loại: 770.11 Inherent features

Thông tin xuất bản: Germany : Journal of neurology , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 98979

 BACKGROUND: Temporal lobe epilepsy with isolated amygdala enlargement (TLE-AE) still lacks a definite characterization and controversies exist. METHODS: We conducted a retrospective study identifying brain MRI scans with isolated AE between 2015 and 2021. We collected clinical and paraclinical data of patients with TLE-AE and evaluated the outcome. RESULTS: Forty-one subjects were included (20 males
  AE: right 13
  left 24
  bilateral 4). A strong correlation was found between AE and MRI T2-hyperintensity (right: p <
  0.005
  left: p <
  0.003). There was no history of febrile seizures
  85,4% had focal seizures with impaired awareness, 78,1% reported auras (epigastric sensation, déjà-vu, anxiety), 37% had psychiatric disturbances, 48,6% presented with cognitive impairment. We report that AE correlates with FDG-PET temporomesial hypometabolism (right: p = 0.022
  left: p = 0.053), temporal interictal activity on EEG (n = 41), and temporal ictal findings during long-term video-EEG monitoring (n = 23). Epilepsy surgery (n = 17) revealed gliosis (n = 4), inflammatory infiltrates (n = 4), or low-grade epilepsy-associated neuroepithelial tumors (n = 5) in the amygdala. Other treatments were immunotherapy (n = 6) and only antiseizure medications (n = 17), with good prognosis (58,1% seizure-free and 17,1% only with auras at last follow-up). There was no correlation between longitudinal changes in seizure frequency and amygdala size (p = 0.848) and T2-hyperintensity (p = 0.909). CONCLUSIONS: AE should be searched in TLE patients with typical aura, psychiatric and/or neurocognitive disturbances. The strong correlations found between AE lateralization and neurophysiological, FDG-PET, and MRI data support involvement of AE in the epileptogenic network. Drug resistance should prompt presurgical study. Inflammation in amygdala specimens and response after immunotherapy suggest an immune-mediated etiology in some TLE-AE cases.
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