Literature DB >> 3680983

Adult cutaneous hemangiomas are composed of nonreplicating endothelial cells.

R M Tuder1, R Young, M Karasek, K Bensch.   

Abstract

Thirty-four human "cherry" dermal hemangiomas were studied by electron microscopy, immunohistochemistry, and cell culture to assess the neoplastic nature of these lesions. Electron microscopy of nine hemangiomas revealed a pronounced thickening of the basement membrane (0.6 to 14 micron) in 93% of the total 158 vascular structures examined within the lesions. This increase was caused mainly by multiple layers of basal lamina, which were irregular in outline and frequently associated with pericytes. Basement membrane changes were present both in the periphery of the hemangiomas, as well as in the center of the lesions. Immature vessels could not be identified and mitoses were absent in all endothelial cells. Using an immunohistochemical marker (Ki67) specific for proliferating cells in G2 and S phases, positive staining was not found in the endothelial cells lining the hemangiomatous vessels, whereas basal epidermal keratinocytes in the same preparations and cultured microvascular endothelial cells expressed the antigen. Endothelial cells of nine hemangiomas did not stain with an activation-related antibody (E12) specific for endothelial cells. When endothelial cells from 14 hemangiomas were isolated and cultured under conditions that support the growth of normal human skin microvascular endothelial cells, the cells of hemangiomatous origin failed to grow. We conclude that the adult hemangiomas may not be true neoplasms, but a tissue overgrowth composed of mature vessels resembling dermal venules, lined by endothelial cells with virtually no turnover.

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Year:  1987        PMID: 3680983     DOI: 10.1111/1523-1747.ep12461306

Source DB:  PubMed          Journal:  J Invest Dermatol        ISSN: 0022-202X            Impact factor:   8.551


  2 in total

1.  Use of Targeted Next-Generation Sequencing to Identify Activating Hot Spot Mutations in Cherry Angiomas.

Authors:  Nikolai Klebanov; William M Lin; Mykyta Artomov; Michael Shaughnessy; Ching-Ni Njauw; Romi Bloom; Agda Karina Eterovic; Ken Chen; Tae-Beom Kim; Sandy S Tsao; Hensin Tsao
Journal:  JAMA Dermatol       Date:  2019-02-01       Impact factor: 10.282

2.  Down-regulation of mir-424 contributes to the abnormal angiogenesis via MEK1 and cyclin E1 in senile hemangioma: its implications to therapy.

Authors:  Taiji Nakashima; Masatoshi Jinnin; Tomomi Etoh; Satoshi Fukushima; Shinichi Masuguchi; Keishi Maruo; Yuji Inoue; Tsuyoshi Ishihara; Hironobu Ihn
Journal:  PLoS One       Date:  2010-12-14       Impact factor: 3.240

  2 in total

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