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Pediatric meningioma with rhabdoid features developed at the site of skull fracture: illustrative case
BACKGROUND: Pediatric meningiomas are rare, and only a few cases attributed to trauma and characterized by development at the site of bone fracture have been reported. Both pediatric and traumatic meningiomas have aggressive characteristics. OBSERVATIONS: An 11-year-old boy who sustained a head inju...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association of Neurological Surgeons
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9563953/ https://www.ncbi.nlm.nih.gov/pubmed/36131573 http://dx.doi.org/10.3171/CASE21107 |
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author | Takata, Sho Tamase, Akira Hayashi, Yasuhiko Tachibana, Osamu Sato, Katsuaki Iizuka, Hideaki |
author_facet | Takata, Sho Tamase, Akira Hayashi, Yasuhiko Tachibana, Osamu Sato, Katsuaki Iizuka, Hideaki |
author_sort | Takata, Sho |
collection | PubMed |
description | BACKGROUND: Pediatric meningiomas are rare, and only a few cases attributed to trauma and characterized by development at the site of bone fracture have been reported. Both pediatric and traumatic meningiomas have aggressive characteristics. OBSERVATIONS: An 11-year-old boy who sustained a head injury resulting from a left frontal skull fracture 8 years previously experienced a convulsive attack. Imaging revealed a meningioma in the left frontal convexity. Total removal of the tumor with a hyperostotic section was successfully achieved. Intraoperative investigation showed tumor invasion into the adjacent frontal cortex. Histologically, the surgical specimen revealed a transitional meningioma with brain invasion and a small cluster of rhabdoid cells. This led to a final pathological diagnosis of an atypical meningioma with rhabdoid features. The postoperative course was uneventful, and no recurrence of the tumor was found after 2 years without adjuvant therapy. LESSONS: This is the first report of a pediatric meningioma with rhabdoid features occurring at the site of a skull fracture. Meningiomas that contain rhabdoid cells without malignant features are not considered to be as aggressive as rhabdoid meningiomas. However, the clinical course must be carefully observed for possible long-term tumor recurrence. |
format | Online Article Text |
id | pubmed-9563953 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Association of Neurological Surgeons |
record_format | MEDLINE/PubMed |
spelling | pubmed-95639532022-10-18 Pediatric meningioma with rhabdoid features developed at the site of skull fracture: illustrative case Takata, Sho Tamase, Akira Hayashi, Yasuhiko Tachibana, Osamu Sato, Katsuaki Iizuka, Hideaki J Neurosurg Case Lessons Case Lesson BACKGROUND: Pediatric meningiomas are rare, and only a few cases attributed to trauma and characterized by development at the site of bone fracture have been reported. Both pediatric and traumatic meningiomas have aggressive characteristics. OBSERVATIONS: An 11-year-old boy who sustained a head injury resulting from a left frontal skull fracture 8 years previously experienced a convulsive attack. Imaging revealed a meningioma in the left frontal convexity. Total removal of the tumor with a hyperostotic section was successfully achieved. Intraoperative investigation showed tumor invasion into the adjacent frontal cortex. Histologically, the surgical specimen revealed a transitional meningioma with brain invasion and a small cluster of rhabdoid cells. This led to a final pathological diagnosis of an atypical meningioma with rhabdoid features. The postoperative course was uneventful, and no recurrence of the tumor was found after 2 years without adjuvant therapy. LESSONS: This is the first report of a pediatric meningioma with rhabdoid features occurring at the site of a skull fracture. Meningiomas that contain rhabdoid cells without malignant features are not considered to be as aggressive as rhabdoid meningiomas. However, the clinical course must be carefully observed for possible long-term tumor recurrence. American Association of Neurological Surgeons 2021-10-04 /pmc/articles/PMC9563953/ /pubmed/36131573 http://dx.doi.org/10.3171/CASE21107 Text en © 2021 The authors https://creativecommons.org/licenses/by-nc-nd/4.0/CC BY-NC-ND 4.0 (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ). |
spellingShingle | Case Lesson Takata, Sho Tamase, Akira Hayashi, Yasuhiko Tachibana, Osamu Sato, Katsuaki Iizuka, Hideaki Pediatric meningioma with rhabdoid features developed at the site of skull fracture: illustrative case |
title | Pediatric meningioma with rhabdoid features developed at the site of skull fracture: illustrative case |
title_full | Pediatric meningioma with rhabdoid features developed at the site of skull fracture: illustrative case |
title_fullStr | Pediatric meningioma with rhabdoid features developed at the site of skull fracture: illustrative case |
title_full_unstemmed | Pediatric meningioma with rhabdoid features developed at the site of skull fracture: illustrative case |
title_short | Pediatric meningioma with rhabdoid features developed at the site of skull fracture: illustrative case |
title_sort | pediatric meningioma with rhabdoid features developed at the site of skull fracture: illustrative case |
topic | Case Lesson |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9563953/ https://www.ncbi.nlm.nih.gov/pubmed/36131573 http://dx.doi.org/10.3171/CASE21107 |
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