Evidence map›Paper›PMID 37308870›Full record

ArticleDiagnostic pathology2023

Completing the view - histologic insights from circular AAA specimen including 3D imaging : A methodologic approach towards histologic analysis of circumferential AAA samples.

Anna-Leonie Menges, Maja Nackenhorst, Johannes R Müller, Marie-Luise Engl, Renate Hegenloh, Jaroslav Pelisek, Ellen Geibelt, Anja Hofmann, Christian Reeps, Gabor Biro and 6 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Diagnostic pathology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.0field-weighted citation impact, top 21% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 7 institutions in 4 countries.

Anna-Leonie MengesDepartment for Vascular Surgery, University Hospital Zurich, Zurich, Switzerland.
Maja NackenhorstDepartment of Pathology, Medical University of Vienna, Vienna, Austria.
Johannes R MüllerDFG Cluster of Excellence "Physics of Life", TU Dresden, Dresden, Germany.
Marie-Luise EnglTechnical University Munich, Department for Vascular and Endovascular Surgery, Klinikum Rechts der Isar, Munich, Germany.
Renate HegenlohTechnical University Munich, Department for Vascular and Endovascular Surgery, Klinikum Rechts der Isar, Munich, Germany.
Jaroslav PelisekDepartment for Vascular Surgery, University Hospital Zurich, Zurich, Switzerland.
Ellen GeibeltLight Microscopy Facility, Center for Molecular and Cellular Bioengineering (CMCB), Technische Universität Dresden, Dresden, Germany.
Anja HofmannDepartment for Visceral-, Thoracic and Vascular Surgery, Medical Faculty and University Hospital Carl Gustav Carus, TUD Dresden University of Technology, Fetscherstrasse 74, Dresden, Germany.
Christian ReepsDepartment for Visceral-, Thoracic and Vascular Surgery, Medical Faculty and University Hospital Carl Gustav Carus, TUD Dresden University of Technology, Fetscherstrasse 74, Dresden, Germany.
Gabor BiroTechnical University Munich, Department for Vascular and Endovascular Surgery, Klinikum Rechts der Isar, Munich, Germany.
Hans-Henning EcksteinTechnical University Munich, Department for Vascular and Endovascular Surgery, Klinikum Rechts der Isar, Munich, Germany.
Alexander ZimmermannDepartment for Vascular Surgery, University Hospital Zurich, Zurich, Switzerland.
Derek MageeHeteroGenius Limited, Leeds, UK.
Martin FalkScientific Visualization Group, Department of Science and Technology (ITN), Linköping University, Linköping, Sweden.
Nadja Sachs *Technical University Munich, Department for Vascular and Endovascular Surgery, Klinikum Rechts der Isar, Munich, Germany.
Albert Busch *Technical University Munich, Department for Vascular and Endovascular Surgery, Klinikum Rechts der Isar, Munich, Germany. albert.busch@uniklinikum-dresden.de.ORCID http://orcid.org/0000-0003-2374-0338
TUM Klinikum · DEUniversity Hospital Carl Gustav Carus · DECenter for Systems Biology Dresden · DELinköping University · SEMedical University of Vienna · ATTechnische Universität Dresden · DEUniversity of Leeds · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Abdominal aortic aneurysm (AAA) is a pathologic enlargement of the infrarenal aorta with an associated risk of rupture. However, the responsible mechanisms are only partially understood. Based on murine and human samples, a heterogeneous distribution of characteristic pathologic features across the aneurysm circumference is expected. Yet, complete histologic workup of the aneurysm sac is scarcely reported. Here, samples from five AAAs covering the complete circumference partially as aortic rings are investigated by histologic means (HE, EvG, immunohistochemistry) and a new method embedding the complete ring. Additionally, two different methods of serial histologic section alignment are applied to create a 3D view. The typical histopathologic features of AAA, elastic fiber degradation, matrix remodeling with collagen deposition, calcification, inflammatory cell infiltration and thrombus coverage were distributed without recognizable pattern across the aneurysm sac in all five patients. Analysis of digitally scanned entire aortic rings facilitates the visualization of these observations. Immunohistochemistry is feasible in such specimen, however, tricky due to tissue disintegration. 3D image stacks were created using open-source and non-generic software correcting for non-rigid warping between consecutive sections. Secondly, 3D image viewers allowed visualization of in-depth changes of the investigated pathologic hallmarks. In conclusion, this exploratory descriptive study demonstrates a heterogeneous histomorphology around the AAA circumference. Warranting an increased sample size, these results might need to be considered in future mechanistic research, especially in reference to intraluminal thrombus coverage. 3D histology of such circular specimen could be a valuable visualization tool for further analysis.

Indexed as

CalcinosisImaging, Three-DimensionalAnimalsHumansMice3D histologyAbdominal Aortic AneurysmAneurysm sacInflammation

Identifiers

PMID37308870
PMCPMC10259026
OpenAlexW4380373996

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.