Detailed histological analysis of a thrombectomy-resistant ischemic stroke thrombus: a case report.

Histology Ischemic stroke NETs Thrombectomy Thrombus composition von Willebrand factor

Journal

Thrombosis journal
ISSN: 1477-9560
Titre abrégé: Thromb J
Pays: England
ID NLM: 101170542

Informations de publication

Date de publication:
22 Feb 2021
Historique:
received: 03 09 2020
accepted: 03 02 2021
entrez: 23 2 2021
pubmed: 24 2 2021
medline: 24 2 2021
Statut: epublish

Résumé

Mechanical removal of a thrombus by thrombectomy can be quite challenging. For reasons that are not fully understood, some thrombi require multiple passes to achieve successful recanalization, whereas other thrombi are efficiently removed in a single pass. Since first pass success is associated with better clinical outcome, it is important to better understand the nature of thrombectomy resistant thrombi. The aim of this study was therefore to characterize the cellular and molecular composition of a thrombus that was very hard to retrieve via mechanical thrombectomy. In a patient that was admitted with a right middle cerebral artery M1-occlusion, 11 attempts using various thrombectomy devices and techniques were required for removal of the thrombus. This peculiar case provided a rare opportunity to perform an in-depth histopathological study of a difficult to retrieve thrombus. Thrombus material was histologically analyzed using hematoxylin and eosin, Martius Scarlet Blue stain (red blood cells and fibrin), Feulgen stain (DNA), von Kossa stain (calcifications) and immunohistochemical analysis of von Willebrand factor, platelets, leukocytes and neutrophil extracellular traps. Histological analysis revealed abnormally high amounts of extracellular DNA, leukocytes, von Willebrand factor and calcifications. Extracellular DNA stained positive for markers of leukocytes and NETs, suggesting that a significant portion of DNA is derived from neutrophil extracellular traps. In this unique case of a nearly thrombectomy-resistant stroke thrombus, our study showed an atypical composition compared to the common structural features found in ischemic stroke thrombi. The core of the retrieved thrombus consisted of extracellular DNA that colocalized with von Willebrand factor and microcalcifications. These results support the hypothesis that von Willebrand factor, neutrophil extracellular traps and microcalcifications contribute to mechanical thrombectomy resistance. Such information is important to identify novel targets in order to optimize technical treatment protocols and techniques to increase first pass success rates.

Sections du résumé

BACKGROUND BACKGROUND
Mechanical removal of a thrombus by thrombectomy can be quite challenging. For reasons that are not fully understood, some thrombi require multiple passes to achieve successful recanalization, whereas other thrombi are efficiently removed in a single pass. Since first pass success is associated with better clinical outcome, it is important to better understand the nature of thrombectomy resistant thrombi. The aim of this study was therefore to characterize the cellular and molecular composition of a thrombus that was very hard to retrieve via mechanical thrombectomy.
CASE PRESENTATION METHODS
In a patient that was admitted with a right middle cerebral artery M1-occlusion, 11 attempts using various thrombectomy devices and techniques were required for removal of the thrombus. This peculiar case provided a rare opportunity to perform an in-depth histopathological study of a difficult to retrieve thrombus. Thrombus material was histologically analyzed using hematoxylin and eosin, Martius Scarlet Blue stain (red blood cells and fibrin), Feulgen stain (DNA), von Kossa stain (calcifications) and immunohistochemical analysis of von Willebrand factor, platelets, leukocytes and neutrophil extracellular traps. Histological analysis revealed abnormally high amounts of extracellular DNA, leukocytes, von Willebrand factor and calcifications. Extracellular DNA stained positive for markers of leukocytes and NETs, suggesting that a significant portion of DNA is derived from neutrophil extracellular traps.
CONCLUSION CONCLUSIONS
In this unique case of a nearly thrombectomy-resistant stroke thrombus, our study showed an atypical composition compared to the common structural features found in ischemic stroke thrombi. The core of the retrieved thrombus consisted of extracellular DNA that colocalized with von Willebrand factor and microcalcifications. These results support the hypothesis that von Willebrand factor, neutrophil extracellular traps and microcalcifications contribute to mechanical thrombectomy resistance. Such information is important to identify novel targets in order to optimize technical treatment protocols and techniques to increase first pass success rates.

Identifiants

pubmed: 33618719
doi: 10.1186/s12959-021-00262-1
pii: 10.1186/s12959-021-00262-1
pmc: PMC7901204
doi:

Types de publication

Journal Article

Langues

eng

Pagination

11

Subventions

Organisme : Fonds Wetenschappelijk Onderzoek
ID : G.0A86.13
Organisme : Fonds Wetenschappelijk Onderzoek
ID : G.0785.17
Organisme : Fonds Wetenschappelijk Onderzoek
ID : 1509216N
Organisme : Onderzoeksraad, KU Leuven
ID : OT/14/099
Organisme : Onderzoeksraad, KU Leuven
ID : ISP/14/02L2
Organisme : Horizon 2020 Research and Innovation Program
ID : INSIST No 777072

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Auteurs

Senna Staessens (S)

Laboratory for Thrombosis Research, KU Leuven Campus Kulak Kortrijk, E. Sabbelaan 53, 8500, Kortrijk, Belgium.

Olivier François (O)

Department of Medical Imaging, AZ Groeninge, Kortrijk, Belgium.

Linda Desender (L)

Laboratory for Thrombosis Research, KU Leuven Campus Kulak Kortrijk, E. Sabbelaan 53, 8500, Kortrijk, Belgium.

Peter Vanacker (P)

Department of Neurology, AZ Groeninge, Kortrijk, Belgium.
Department of Neurology, University Hospitals Antwerp, Antwerp, Belgium.
Department of Translational Neuroscience, University of Antwerp, Antwerp, Belgium.

Tom Dewaele (T)

Department of Medical Imaging, AZ Groeninge, Kortrijk, Belgium.

Raf Sciot (R)

Department of Pathology, University Hospitals KU Leuven, Leuven, Belgium.

Karen Vanhoorelbeke (K)

Laboratory for Thrombosis Research, KU Leuven Campus Kulak Kortrijk, E. Sabbelaan 53, 8500, Kortrijk, Belgium.

Tommy Andersson (T)

Department of Medical Imaging, AZ Groeninge, Kortrijk, Belgium.
Departments of Neuroradiology, Karolinska University Hospital, and Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden.

Simon F De Meyer (SF)

Laboratory for Thrombosis Research, KU Leuven Campus Kulak Kortrijk, E. Sabbelaan 53, 8500, Kortrijk, Belgium. simon.demeyer@kuleuven.be.

Classifications MeSH