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      Multifocal kaposiform haemangioendothelioma.

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          Abstract

          Kaposiform haemangioendothelioma (KHE) is a rare, locally aggressive vascular spindle cell proliferation, with resemblance to Kaposi's sarcoma. This tumour usually occurs in skin and retroperitoneum of infants and young children and is often complicated by the Kasabach-Merritt phenomenon (KMP). A 3-year-old boy presented with a right submandibular swelling due to lymphadenopathies, a violaceous skin lesion at the left commissure of the lips and an ill-defined lesion in the right thyroid lobe. There were some signs of KMP. Histological examination revealed a typical infiltrative multilobular spindle cell proliferation with slit-like vascular spaces in these three localisations. Immunohistochemical stains showed positivity for CD34 and CD31 and many alpha-smooth muscle actin-positive spindle cells around the vascular spaces. There was no Herpes virus type 8 expression. The presented case is unique in two ways. First, thyroid involvement of KHE has never been described in the literature until now. Secondly, and most remarkably, the multifocal presentation in three anatomically distinct and separated localisations is extremely unusual.

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          Author and article information

          Journal
          Virchows Arch
          Virchows Archiv : an international journal of pathology
          Springer Science and Business Media LLC
          0945-6317
          0945-6317
          Jun 2006
          : 448
          : 6
          Affiliations
          [1 ] Department of Pathology, University Hospital St. Rafaël, Katholieke Universiteit Leuven, Minderbroedersstraat 12, 3000 Leuven, Belgium.
          Article
          10.1007/s00428-006-0177-6
          16596383
          add2343a-ad3b-431c-bcef-5e5ecd786be2
          History

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