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Hyaline eosinophilic astrocytic inclusions in two children with drug-resistant epilepsy—Case reports and literature review

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dc.contributor.author Mezmezian, Mónica Beatriz
dc.contributor.author Arakaki, Naomi
dc.contributor.author Yáñez, Paulina
dc.contributor.author Arias Cebollada, Eugenia
dc.contributor.author Muro, Valeria L.
dc.contributor.author Sevlever, Gustavo Emilio
dc.date.accessioned 2024-06-19T15:56:37Z
dc.date.available 2024-06-19T15:56:37Z
dc.date.issued 2023-09-13
dc.identifier.citation Mezmezian MB, Arakaki N, Yáñez P, Arias Cebollada E, Muro VL, Sevlever GE. Hyaline eosinophilic astrocytic inclusions in two children with drug-resistant epilepsy—Case reports and literature review. Brain Pathology. 2023 Sep;33 Suppl 1(Suppl 1, Abstracts of the 20th International Congress of Neuropathology Berlin, Germany):e13194 es_ES
dc.identifier.uri https://doi.org/10.1111/bpa.13194
dc.identifier.uri https://repositorio.fleni.org.ar/xmlui/handle/123456789/1135
dc.description.abstract Introduction: Hyaline eosinophilic astrocytic inclusion (HEAI) is a rare histological finding in cases with drugresistant epilepsy (DRE). Objectives: To describe two cases of DRE with HEAI and review the literature. Patients and Methods: Case 1: A 5-year-old boy with a history of DRE since 5 months of age and global developmental delay, nonverbal (GDD, NV). MRI revealed signs of polymicrogyria, involving the right frontal operculum with an abnormal cortical folding and rotation pattern. The genetic panel showed a variant of uncertain significance in the SCL2A1 gene. Outcome: Engel IV-B. Case 2: A 5-year-old boy with a history of DRE since 4 months of age and GDD, NV. MRI showed abnormal cortical folding and cortical thickening in the right frontal lobe. Genetic testing demonstrated a variant of uncertain significance in the ADAR gene. Outcome: Engel IV-A. Resection of the lesion was performed in both patients. Results: Both cases showed brightly eosinophilic structures within the astrocytic cytoplasm in the gray matter and FCD type 2A. The inclusions were negative with PAS and Congo red. By immunohistochemistry, they were positive for S100 and negative for vimentin, and GFAP. We also analyzed the data of all the previously reported cases. Conclusion: HEAI is a rare entity, with only 53 cases reported, including our cases. Evaluating all the cases, the average age at seizure onset of pediatric patients (n = 48) was 7 months, without sex predilection. Seven patients had Aicardi syndrome, and 23 patients presented GDD. Seizures were observed in 47 patients. Outcome Engel: I in 10 cases, II in 5, III in 9, and IV in 9. Most cases involved the frontal lobe (n = 40). HEAIs were positive for S100 in 21/25 (84%), filamin in 22/25 (88%), GFAP in 3/32 cases (9%), vimentin in 1/16 (6%), and PAS in 3/21 (14%). FCD was observed in 19/50 patients (38%). The significance of HEAI is not clear. Genetic studies of the surgical specimens will probably allow a better comprehension of this entity. es_ES
dc.language.iso eng es_ES
dc.publisher Wiley es_ES
dc.subject Drug Resistant Epilepsy es_ES
dc.subject Epilepsia Refractaria es_ES
dc.subject Astrocytes es_ES
dc.subject Astrocitos es_ES
dc.subject Hyalin es_ES
dc.subject Hialina es_ES
dc.title Hyaline eosinophilic astrocytic inclusions in two children with drug-resistant epilepsy—Case reports and literature review es_ES
dc.type Presentation es_ES
dc.description.fil Fil: Mezmezian, Mónica Beatriz. Fleni. Departamento de Neuropatología y Biología Molecular; Argentina.
dc.description.fil Fil: Arakaki, Naomi. Fleni. Departamento de Neuropatología y Biología Molecular; Argentina.
dc.description.fil Fil: Yáñez, Paulina. Fleni. Departamento de Diagnóstico por Imágenes; Argentina.
dc.description.fil Fil: Arias Cebollada, Eugenia. Fleni. Departamento de Neuropatología y Biología Molecular; Argentina.
dc.description.fil Fil: Muro, Valeria L. Fleni. Centro Integral de Epilepsia y Unidad de Monitoreo de Videoelectroencefalografía; Argentina.
dc.description.fil Fil: Sevlever, Gustavo Emilio. Fleni. Departamento de Neuropatología y Biología Molecular; Argentina.
dc.relation.ispartofVOLUME 33
dc.relation.ispartofNUMBER Issue S1
dc.relation.ispartofPAGINATION 179
dc.relation.ispartofCOUNTRY Suiza
dc.relation.ispartofCITY Zürich
dc.relation.ispartofTITLE Brain Pathology
dc.relation.ispartofISSN 1750-3639
dc.type.snrd Presentation es_ES


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