File:PMC4056107 fimmu-05-00281-g001.png

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PMC4056107_fimmu-05-00281-g001.png(512 × 130 pixels, file size: 166 KB, MIME type: image/png)

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Attribution 3.0 Unported (CC BY 3.0)

Summary

Author:Cavalli G, Biavasco R, Borgiani B, Dagna L , Unit of Internal Medicine and Clinical Immunology, IRCCS San Raffaele Scientific Institute (Openi/National Library of Medicine) Source:https://openi.nlm.nih.gov/detailedresult?img=PMC4056107_fimmu-05-00281-g001&query=Erdheim%E2%80%93Chester%20disease&it=xg&req=4&npos=2 Description:F1: Histological findings in patients with Erdheim–Chester disease (ECD). Histology shows a xanthogranulomatous infiltrate composed by foamy histiocytes accompanied by fibrosis [(A), H&E, original magnification 200×]. Immunohistochemical studies reveal that some of the infiltrating histiocytes stain for BRAFV600E [(B), VE1 immunostaining, 200×], and p16Ink4a [(C), p16Ink4a immunostaining, 200×].

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current20:59, 24 October 2021Thumbnail for version as of 20:59, 24 October 2021512 × 130 (166 KB)Ozzie10aaaa (talk | contribs)Author:Cavalli G, Biavasco R, Borgiani B, Dagna L , Unit of Internal Medicine and Clinical Immunology, IRCCS San Raffaele Scientific Institute (Openi/National Library of Medicine) Source:https://openi.nlm.nih.gov/detailedresult?img=PMC4056107_fimmu-05-00281-g001&query=Erdheim%E2%80%93Chester%20disease&it=xg&req=4&npos=2 Description:F1: Histological findings in patients with Erdheim–Chester disease (ECD). Histology shows a xanthogranulomatous infiltrate composed by foamy histiocytes accompanie...

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