Myopericytoma and arterial intimal thickening: the relationship between myopericytes and myointimal cells

Background: Myopericytomas with intravascular growth have been reported and have been occasionally documented as intraarterial. In a retrospective study, we assessed intraarterial growth in myopericytomas, co‐existence with arterial intimal thickening (IT) and the relationship between the two. Metho...

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Veröffentlicht in:Journal of cutaneous pathology 2011-11, Vol.38 (11), p.857-864
Hauptverfasser: Díaz-Flores, Lucio, Gutiérrez, Ricardo, García, Maria P., Álvarez-Argüelles, Hugo, Díaz-Flores Jr, Lucio, Madrid, Juan F.
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container_end_page 864
container_issue 11
container_start_page 857
container_title Journal of cutaneous pathology
container_volume 38
creator Díaz-Flores, Lucio
Gutiérrez, Ricardo
García, Maria P.
Álvarez-Argüelles, Hugo
Díaz-Flores Jr, Lucio
Madrid, Juan F.
description Background: Myopericytomas with intravascular growth have been reported and have been occasionally documented as intraarterial. In a retrospective study, we assessed intraarterial growth in myopericytomas, co‐existence with arterial intimal thickening (IT) and the relationship between the two. Methods: This retrospective study was undertaken using 11 myopericytomas evaluated in serial microscopical sections. The results in light microscopy, electron microscopy and immunohistochemistry [including α‐smooth muscle actin (SMA), desmin and h‐caldesmon] were evaluated. Results: In four myopericytomas, we found intraarterial growth, with large areas of disrupted arterial wall and attachment of veins and venules, exhibiting angiogenic phenomena. Arterial IT was present and partially incorporated within the tumor (simulating medium‐sized vessels). The neointimal (myointimal) cells shared morphological and immunohistochemical phenotype with the myopericytoma myoid cells, including α‐SMA positivity and desmin negativity. Four of the remaining myopericytomas showed structures similar to arterial IT within the tumor. Conclusions: The findings shown here, including the association between myopericytomas and arterial IT, the incorporation of the latter into the tumor and the similar phenotype of their respective myoid and myointimal cells, support a close relationship between these processes. Histogenically, the pericytes of the penetrating neovasculature originating from the attached venules and veins may contribute to both lesions. Díaz‐Flores L, Gutiérrez R, García MP, Álvarez‐Argüelles H, Díaz‐Flores L Jr, Madrid JF. Myopericytoma and arterial intimal thickening: the relationship between myopericytes and myointimal cells.
doi_str_mv 10.1111/j.1600-0560.2011.01778.x
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In a retrospective study, we assessed intraarterial growth in myopericytomas, co‐existence with arterial intimal thickening (IT) and the relationship between the two. Methods: This retrospective study was undertaken using 11 myopericytomas evaluated in serial microscopical sections. The results in light microscopy, electron microscopy and immunohistochemistry [including α‐smooth muscle actin (SMA), desmin and h‐caldesmon] were evaluated. Results: In four myopericytomas, we found intraarterial growth, with large areas of disrupted arterial wall and attachment of veins and venules, exhibiting angiogenic phenomena. Arterial IT was present and partially incorporated within the tumor (simulating medium‐sized vessels). The neointimal (myointimal) cells shared morphological and immunohistochemical phenotype with the myopericytoma myoid cells, including α‐SMA positivity and desmin negativity. Four of the remaining myopericytomas showed structures similar to arterial IT within the tumor. Conclusions: The findings shown here, including the association between myopericytomas and arterial IT, the incorporation of the latter into the tumor and the similar phenotype of their respective myoid and myointimal cells, support a close relationship between these processes. Histogenically, the pericytes of the penetrating neovasculature originating from the attached venules and veins may contribute to both lesions. Díaz‐Flores L, Gutiérrez R, García MP, Álvarez‐Argüelles H, Díaz‐Flores L Jr, Madrid JF. 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In a retrospective study, we assessed intraarterial growth in myopericytomas, co‐existence with arterial intimal thickening (IT) and the relationship between the two. Methods: This retrospective study was undertaken using 11 myopericytomas evaluated in serial microscopical sections. The results in light microscopy, electron microscopy and immunohistochemistry [including α‐smooth muscle actin (SMA), desmin and h‐caldesmon] were evaluated. Results: In four myopericytomas, we found intraarterial growth, with large areas of disrupted arterial wall and attachment of veins and venules, exhibiting angiogenic phenomena. Arterial IT was present and partially incorporated within the tumor (simulating medium‐sized vessels). The neointimal (myointimal) cells shared morphological and immunohistochemical phenotype with the myopericytoma myoid cells, including α‐SMA positivity and desmin negativity. Four of the remaining myopericytomas showed structures similar to arterial IT within the tumor. Conclusions: The findings shown here, including the association between myopericytomas and arterial IT, the incorporation of the latter into the tumor and the similar phenotype of their respective myoid and myointimal cells, support a close relationship between these processes. Histogenically, the pericytes of the penetrating neovasculature originating from the attached venules and veins may contribute to both lesions. Díaz‐Flores L, Gutiérrez R, García MP, Álvarez‐Argüelles H, Díaz‐Flores L Jr, Madrid JF. 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Gutiérrez, Ricardo ; García, Maria P. ; Álvarez-Argüelles, Hugo ; Díaz-Flores Jr, Lucio ; Madrid, Juan F.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5028-7c7411c23631e465ee7225ddda66b530e29b080a6e0c43ab9ffab0e80c01269d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Actins - metabolism</topic><topic>Adult</topic><topic>Aged</topic><topic>Biological and medical sciences</topic><topic>Biomarkers, Tumor - metabolism</topic><topic>Calmodulin-Binding Proteins - metabolism</topic><topic>Dermatology</topic><topic>Desmin - metabolism</topic><topic>Female</topic><topic>Hemangiopericytoma - metabolism</topic><topic>Hemangiopericytoma - pathology</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Muscle, Smooth, Vascular - metabolism</topic><topic>Muscle, Smooth, Vascular - pathology</topic><topic>Myocytes, Smooth Muscle - metabolism</topic><topic>Myocytes, Smooth Muscle - pathology</topic><topic>myointimal cells</topic><topic>myopericytes</topic><topic>myopericytoma</topic><topic>neointimal cells</topic><topic>pericytes</topic><topic>Pericytes - metabolism</topic><topic>Pericytes - pathology</topic><topic>Retrospective Studies</topic><topic>Skin Neoplasms - metabolism</topic><topic>Skin Neoplasms - pathology</topic><topic>Tunica Intima - metabolism</topic><topic>Tunica Intima - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Díaz-Flores, Lucio</creatorcontrib><creatorcontrib>Gutiérrez, Ricardo</creatorcontrib><creatorcontrib>García, Maria P.</creatorcontrib><creatorcontrib>Álvarez-Argüelles, Hugo</creatorcontrib><creatorcontrib>Díaz-Flores Jr, Lucio</creatorcontrib><creatorcontrib>Madrid, Juan F.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of cutaneous pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Díaz-Flores, Lucio</au><au>Gutiérrez, Ricardo</au><au>García, Maria P.</au><au>Álvarez-Argüelles, Hugo</au><au>Díaz-Flores Jr, Lucio</au><au>Madrid, Juan F.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Myopericytoma and arterial intimal thickening: the relationship between myopericytes and myointimal cells</atitle><jtitle>Journal of cutaneous pathology</jtitle><addtitle>J Cutan Pathol</addtitle><date>2011-11</date><risdate>2011</risdate><volume>38</volume><issue>11</issue><spage>857</spage><epage>864</epage><pages>857-864</pages><issn>0303-6987</issn><eissn>1600-0560</eissn><coden>JCUPBN</coden><abstract>Background: Myopericytomas with intravascular growth have been reported and have been occasionally documented as intraarterial. In a retrospective study, we assessed intraarterial growth in myopericytomas, co‐existence with arterial intimal thickening (IT) and the relationship between the two. Methods: This retrospective study was undertaken using 11 myopericytomas evaluated in serial microscopical sections. The results in light microscopy, electron microscopy and immunohistochemistry [including α‐smooth muscle actin (SMA), desmin and h‐caldesmon] were evaluated. Results: In four myopericytomas, we found intraarterial growth, with large areas of disrupted arterial wall and attachment of veins and venules, exhibiting angiogenic phenomena. Arterial IT was present and partially incorporated within the tumor (simulating medium‐sized vessels). The neointimal (myointimal) cells shared morphological and immunohistochemical phenotype with the myopericytoma myoid cells, including α‐SMA positivity and desmin negativity. Four of the remaining myopericytomas showed structures similar to arterial IT within the tumor. Conclusions: The findings shown here, including the association between myopericytomas and arterial IT, the incorporation of the latter into the tumor and the similar phenotype of their respective myoid and myointimal cells, support a close relationship between these processes. Histogenically, the pericytes of the penetrating neovasculature originating from the attached venules and veins may contribute to both lesions. Díaz‐Flores L, Gutiérrez R, García MP, Álvarez‐Argüelles H, Díaz‐Flores L Jr, Madrid JF. Myopericytoma and arterial intimal thickening: the relationship between myopericytes and myointimal cells.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>21955312</pmid><doi>10.1111/j.1600-0560.2011.01778.x</doi><tpages>8</tpages></addata></record>
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subjects Actins - metabolism
Adult
Aged
Biological and medical sciences
Biomarkers, Tumor - metabolism
Calmodulin-Binding Proteins - metabolism
Dermatology
Desmin - metabolism
Female
Hemangiopericytoma - metabolism
Hemangiopericytoma - pathology
Humans
Male
Medical sciences
Middle Aged
Muscle, Smooth, Vascular - metabolism
Muscle, Smooth, Vascular - pathology
Myocytes, Smooth Muscle - metabolism
Myocytes, Smooth Muscle - pathology
myointimal cells
myopericytes
myopericytoma
neointimal cells
pericytes
Pericytes - metabolism
Pericytes - pathology
Retrospective Studies
Skin Neoplasms - metabolism
Skin Neoplasms - pathology
Tunica Intima - metabolism
Tunica Intima - pathology
title Myopericytoma and arterial intimal thickening: the relationship between myopericytes and myointimal cells
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