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Lymphoedema is a potential sequela of Kaposiform haemangioendothelioma: reply from the authors.

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Title: Lymphoedema is a potential sequela of Kaposiform haemangioendothelioma: reply from the authors.
Authors: Boccara O; Department of Dermatology and Reference Center for Genodermatoses and Rare Skin Diseases (MAGEC), Université Paris Descartes - Sorbonne Paris Cité, Institut Imagine, Hôpital Universitaire Necker-Enfants Malades, 149 Rue de Sèvres, 75015, Paris, France. olivia.boccara@aphp.fr., Hadj-Rabia S; Department of Dermatology and Reference Center for Genodermatoses and Rare Skin Diseases (MAGEC), Université Paris Descartes - Sorbonne Paris Cité, Institut Imagine, Hôpital Universitaire Necker-Enfants Malades, 149 Rue de Sèvres, 75015, Paris, France., Bourrat E; Department of General Paediatrics, Robert-Debré Hospital, Paris, France., Coulombe J; Department of Dermatology and Reference Center for Genodermatoses and Rare Skin Diseases (MAGEC), Université Paris Descartes - Sorbonne Paris Cité, Institut Imagine, Hôpital Universitaire Necker-Enfants Malades, 149 Rue de Sèvres, 75015, Paris, France., Bodemer C; Department of Dermatology and Reference Center for Genodermatoses and Rare Skin Diseases (MAGEC), Université Paris Descartes - Sorbonne Paris Cité, Institut Imagine, Hôpital Universitaire Necker-Enfants Malades, 149 Rue de Sèvres, 75015, Paris, France.
Source: The British journal of dermatology [Br J Dermatol] 2016 Oct; Vol. 175 (4), pp. 834. Date of Electronic Publication: 2016 Aug 11.
Publication Type: Letter; Comment
Journal Info: Publisher: Oxford University Press Country of Publication: England NLM ID: 0004041 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1365-2133 (Electronic) Linking ISSN: 00070963 NLM ISO Abbreviation: Br J Dermatol Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Lymphoedema is a potential sequela of Kaposiform haemangioendothelioma: reply from the authors.
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  Data: <searchLink fieldCode="AU" term="%22Boccara+O%22">Boccara O</searchLink>; Department of Dermatology and Reference Center for Genodermatoses and Rare Skin Diseases (MAGEC), Université Paris Descartes - Sorbonne Paris Cité, Institut Imagine, Hôpital Universitaire Necker-Enfants Malades, 149 Rue de Sèvres, 75015, Paris, France. olivia.boccara@aphp.fr.<br /><searchLink fieldCode="AU" term="%22Hadj-Rabia+S%22">Hadj-Rabia S</searchLink>; Department of Dermatology and Reference Center for Genodermatoses and Rare Skin Diseases (MAGEC), Université Paris Descartes - Sorbonne Paris Cité, Institut Imagine, Hôpital Universitaire Necker-Enfants Malades, 149 Rue de Sèvres, 75015, Paris, France.<br /><searchLink fieldCode="AU" term="%22Bourrat+E%22">Bourrat E</searchLink>; Department of General Paediatrics, Robert-Debré Hospital, Paris, France.<br /><searchLink fieldCode="AU" term="%22Coulombe+J%22">Coulombe J</searchLink>; Department of Dermatology and Reference Center for Genodermatoses and Rare Skin Diseases (MAGEC), Université Paris Descartes - Sorbonne Paris Cité, Institut Imagine, Hôpital Universitaire Necker-Enfants Malades, 149 Rue de Sèvres, 75015, Paris, France.<br /><searchLink fieldCode="AU" term="%22Bodemer+C%22">Bodemer C</searchLink>; Department of Dermatology and Reference Center for Genodermatoses and Rare Skin Diseases (MAGEC), Université Paris Descartes - Sorbonne Paris Cité, Institut Imagine, Hôpital Universitaire Necker-Enfants Malades, 149 Rue de Sèvres, 75015, Paris, France.
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