Published ahead of print on January 17, 2008
doi: 10.3174/ajnr.A0902
Mechanisms of Occlusion and Recanalization in Canine Carotid Bifurcation Aneurysms Embolized with Platinum Coils: An Alternative Concept
J. Raymonda,
T. Darsauta,b,
I. Salazkina,
G. Gevrya and
F. Bouzeghranea
a Interventional Neuroradiology Laboratory, CHUM Research Centre, Centre Hospitalier de l'Université de Montréal-Hôpital Notre-Dame, Quebec, Canada
b Department of Surgery, Division of Neurosurgery, University of Alberta, Edmonton, Alberta, Canada

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Fig 2. Angiographic and macroscopic results. Angiography (A, C, E) and macroscopic photographs (B, D, F) of prototypical cases of recurrence at 3 months and poor neointimal closure (A and B), complete occlusions at 3 months with good neointimal closure of the neck (C and D), and angiographic occlusion but with poor neointimal closure of the neck (E and F). Note that the coils have been removed in D.
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Fig 5. Common findings of occluded and recurrent aneurysms. Macroscopic views with coils protruding into the lumen vessel before (A) and after coil retrieval (B). Note that all coils are re-covered with neointima, which consists of smooth muscle (SM) cells (C) embedded in a collagenous matrix surrounded by a unique layer of NOS+ cells (D). Note polypoid filaments (pink arrows in A and E) observed at the neck of aneurysms, with a similar neointima organization (F). Sections are hematoxylin-counterstained (scale bar: 200 µm for C, D, and F; 40 µm for insets in C, D, and F).
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Fig 6. Vascularized connective tissues are similarly organized in occluded (A and C) and recurrent (B and D) aneurysm with smooth muscle (SM) –actin+ cells, presumably myofibroblast (A and B) and NOS+ cells for neovascularization (C and D) (scale bar: 200 µm).
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Fig 7. Tissues infiltrating the core of the coils. Immunostaining of smooth muscle (SM) –actin (A), of NOS (B), and Movat pentachrome stain (C) shows the same structure as the vascularized tissue inside the aneurysm (scale bar: 200 µm).
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