Pathologic Features of Brain Hemorrhage After Radiation Treatment: Case Series with Somatic Mutation Analysis.

adverse radiation effects case series hemorrhage mutation stereotactic radiosurgery

Journal

Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association
ISSN: 1532-8511
Titre abrégé: J Stroke Cerebrovasc Dis
Pays: United States
ID NLM: 9111633

Informations de publication

Date de publication:
27 Mar 2024
Historique:
received: 25 10 2023
revised: 15 03 2024
accepted: 26 03 2024
medline: 30 3 2024
pubmed: 30 3 2024
entrez: 29 3 2024
Statut: aheadofprint

Résumé

Radiation treatment for diseases of the brain can result in hemorrhagic adverse radiation effects. The underlying pathologic substrate of brain bleeding after irradiation has not been elucidated, nor potential associations with induced somatic mutations. We retrospectively reviewed our department's pathology database over 5 years and identified 5 biopsy specimens (4 patients) for hemorrhagic lesions after brain irradiation. Tissues with active malignancy were excluded. Samples were characterized using H&E, Perl's Prussian Blue, and Masson's Trichrome; immunostaining for B-cells (anti-CD20), T-cells (anti-CD3), endothelium (anti-CD31), macrophages (anti-CD163), α-smooth muscle actin, and TUNEL. DNA analysis was done by two panels of next-generation sequencing for somatic mutations associated with known cerebrovascular anomalies. One lesion involved hemorrhagic expansion among multifocal microbleeds that had developed after craniospinal irradiation for distant medulloblastoma treatment. Three bleeds arose in the bed of focally irradiated arteriovenous malformations (AVM) after confirmed obliteration. A fifth specimen involved the radiation field distinct from an irradiated AVM bed. From these, 2 patterns of hemorrhagic vascular pathology were identified: encapsulated hematomas and cavernous-like malformations. All lesions included telangiectasias with dysmorphic endothelium, consistent with primordial cavernous malformations with an associated inflammatory response. DNA analysis demonstrated genetic variants in PIK3CA and/or PTEN genes but excluded mutations in CCM genes. Despite pathologic heterogeneity, brain bleeding after irradiation is uniformly associated with primordial cavernous-like telangiectasias and disruption of genes implicated in dysangiogenesis but not genes implicated as causative of cerebral cavernous malformations. This may implicate a novel signaling axis as an area for future study.

Sections du résumé

BACKGROUND BACKGROUND
Radiation treatment for diseases of the brain can result in hemorrhagic adverse radiation effects. The underlying pathologic substrate of brain bleeding after irradiation has not been elucidated, nor potential associations with induced somatic mutations.
METHODS METHODS
We retrospectively reviewed our department's pathology database over 5 years and identified 5 biopsy specimens (4 patients) for hemorrhagic lesions after brain irradiation. Tissues with active malignancy were excluded. Samples were characterized using H&E, Perl's Prussian Blue, and Masson's Trichrome; immunostaining for B-cells (anti-CD20), T-cells (anti-CD3), endothelium (anti-CD31), macrophages (anti-CD163), α-smooth muscle actin, and TUNEL. DNA analysis was done by two panels of next-generation sequencing for somatic mutations associated with known cerebrovascular anomalies.
RESULTS RESULTS
One lesion involved hemorrhagic expansion among multifocal microbleeds that had developed after craniospinal irradiation for distant medulloblastoma treatment. Three bleeds arose in the bed of focally irradiated arteriovenous malformations (AVM) after confirmed obliteration. A fifth specimen involved the radiation field distinct from an irradiated AVM bed. From these, 2 patterns of hemorrhagic vascular pathology were identified: encapsulated hematomas and cavernous-like malformations. All lesions included telangiectasias with dysmorphic endothelium, consistent with primordial cavernous malformations with an associated inflammatory response. DNA analysis demonstrated genetic variants in PIK3CA and/or PTEN genes but excluded mutations in CCM genes.
CONCLUSIONS CONCLUSIONS
Despite pathologic heterogeneity, brain bleeding after irradiation is uniformly associated with primordial cavernous-like telangiectasias and disruption of genes implicated in dysangiogenesis but not genes implicated as causative of cerebral cavernous malformations. This may implicate a novel signaling axis as an area for future study.

Identifiants

pubmed: 38552890
pii: S1052-3057(24)00144-7
doi: 10.1016/j.jstrokecerebrovasdis.2024.107699
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

107699

Informations de copyright

Copyright © 2024. Published by Elsevier Inc.

Déclaration de conflit d'intérêts

Declaration of competing interest Drs. Awad and Marchuk receive grant funding from the U.S. National Institutes of Health and the Department of Defense. Dr. Awad is a consultant to Neurelis, Inc. The other authors report no conflicts

Auteurs

Roberto J Alcazar-Felix (RJ)

Section of Neurosurgery, Biological Sciences Division, University of Chicago.

Abhinav Srinath (A)

Section of Neurosurgery, Biological Sciences Division, University of Chicago.

Stephanie Hage (S)

Section of Neurosurgery, Biological Sciences Division, University of Chicago.

Akash Bindal (A)

Section of Neurosurgery, Biological Sciences Division, University of Chicago.

Andrew Ressler (A)

Molecular Genetics and Microbiology Department, Duke University Medical Center.

Peter Pytel (P)

Section of Neurosurgery, Biological Sciences Division, University of Chicago.

Sammy Allaw (S)

Section of Neurosurgery, Biological Sciences Division, University of Chicago.

Romuald Girard (R)

Section of Neurosurgery, Biological Sciences Division, University of Chicago.

Douglas A Marchuk (DA)

Molecular Genetics and Microbiology Department, Duke University Medical Center.

Issam A Awad (IA)

Section of Neurosurgery, Biological Sciences Division, University of Chicago.

Sean P Polster (SP)

Section of Neurosurgery, Biological Sciences Division, University of Chicago.. Electronic address: seanpolster@gmail.com.

Classifications MeSH