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Trametinib for multiple non-ossifying fibromas due to KRAS mosaic mutations: two case reports.

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Title: Trametinib for multiple non-ossifying fibromas due to KRAS mosaic mutations: two case reports.
Authors: Vincent M; Service de Génétique Médicale, CHU Nantes, Nantes, France. marie.vincent@chu-nantes.fr.; Institut du thorax, INSERM, CNRS, UNIV, Nantes, France. marie.vincent@chu-nantes.fr., Tiriau S; Service de Pédiatrie-Spécialités, CHU Nantes, Nantes, France., Fouillet-Desjonqueres M; Service de Néphrologie-Rhumatologie-Dermatologie Pédiatriques, Hospices Civils de, Lyon, France.; Centre de référence des Maladies Osseuses Constitutionnelles, Hospices Civils de, Lyon, France., Besson A; Université Claude Bernard Lyon 1, CNRS, INSERM, Centre de Recherche en Neurosciences de Lyon CRNL U1028 UMR5292, GENDEV, Bron, France., Ouchetto W; Université Claude Bernard Lyon 1, CNRS, INSERM, Centre de Recherche en Neurosciences de Lyon CRNL U1028 UMR5292, GENDEV, Bron, France., Barbarot S; Service de Dermatologie, CHU Nantes, Nantes, France., Isidor B; Service de Génétique Médicale, CHU Nantes, Nantes, France.; Institut du thorax, INSERM, CNRS, UNIV, Nantes, France., Rouchaud A; Service d'Imagerie Médicale, Hospices Civils de, Lyon, France., Baujat G; Service de Génétique Médicale, Centre de Référence des Maladies Osseuses Constitutionnelles, Hôpital Necker-Enfants Malades, APHP, Paris, France., Vabres P; Service de Dermatologie, CHU Dijon Bourgogne, Dijon, France., Edery P; Université Claude Bernard Lyon 1, CNRS, INSERM, Centre de Recherche en Neurosciences de Lyon CRNL U1028 UMR5292, GENDEV, Bron, France.; Service de Génétique, Hospices Civils de, Lyon, France., Delous M; Université Claude Bernard Lyon 1, CNRS, INSERM, Centre de Recherche en Neurosciences de Lyon CRNL U1028 UMR5292, GENDEV, Bron, France., Rossi M; Centre de référence des Maladies Osseuses Constitutionnelles, Hospices Civils de, Lyon, France.; Université Claude Bernard Lyon 1, CNRS, INSERM, Centre de Recherche en Neurosciences de Lyon CRNL U1028 UMR5292, GENDEV, Bron, France.; Service de Génétique, Hospices Civils de, Lyon, France.
Source: Communications medicine [Commun Med (Lond)] 2026 May 18. Date of Electronic Publication: 2026 May 18.
Publication Type: Journal Article
Journal Info: Publisher: Nature Portfolio Country of Publication: England NLM ID: 9918250414506676 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2730-664X (Electronic) Linking ISSN: 2730664X NLM ISO Abbreviation: Commun Med (Lond)
Database: MEDLINE Ultimate
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  Data: Trametinib for multiple non-ossifying fibromas due to KRAS mosaic mutations: two case reports.
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  Data: <searchLink fieldCode="AU" term="%22Vincent+M%22">Vincent M</searchLink>; Service de Génétique Médicale, CHU Nantes, Nantes, France. marie.vincent@chu-nantes.fr.; Institut du thorax, INSERM, CNRS, UNIV, Nantes, France. marie.vincent@chu-nantes.fr.<br /><searchLink fieldCode="AU" term="%22Tiriau+S%22">Tiriau S</searchLink>; Service de Pédiatrie-Spécialités, CHU Nantes, Nantes, France.<br /><searchLink fieldCode="AU" term="%22Fouillet-Desjonqueres+M%22">Fouillet-Desjonqueres M</searchLink>; Service de Néphrologie-Rhumatologie-Dermatologie Pédiatriques, Hospices Civils de, Lyon, France.; Centre de référence des Maladies Osseuses Constitutionnelles, Hospices Civils de, Lyon, France.<br /><searchLink fieldCode="AU" term="%22Besson+A%22">Besson A</searchLink>; Université Claude Bernard Lyon 1, CNRS, INSERM, Centre de Recherche en Neurosciences de Lyon CRNL U1028 UMR5292, GENDEV, Bron, France.<br /><searchLink fieldCode="AU" term="%22Ouchetto+W%22">Ouchetto W</searchLink>; Université Claude Bernard Lyon 1, CNRS, INSERM, Centre de Recherche en Neurosciences de Lyon CRNL U1028 UMR5292, GENDEV, Bron, France.<br /><searchLink fieldCode="AU" term="%22Barbarot+S%22">Barbarot S</searchLink>; Service de Dermatologie, CHU Nantes, Nantes, France.<br /><searchLink fieldCode="AU" term="%22Isidor+B%22">Isidor B</searchLink>; Service de Génétique Médicale, CHU Nantes, Nantes, France.; Institut du thorax, INSERM, CNRS, UNIV, Nantes, France.<br /><searchLink fieldCode="AU" term="%22Rouchaud+A%22">Rouchaud A</searchLink>; Service d'Imagerie Médicale, Hospices Civils de, Lyon, France.<br /><searchLink fieldCode="AU" term="%22Baujat+G%22">Baujat G</searchLink>; Service de Génétique Médicale, Centre de Référence des Maladies Osseuses Constitutionnelles, Hôpital Necker-Enfants Malades, APHP, Paris, France.<br /><searchLink fieldCode="AU" term="%22Vabres+P%22">Vabres P</searchLink>; Service de Dermatologie, CHU Dijon Bourgogne, Dijon, France.<br /><searchLink fieldCode="AU" term="%22Edery+P%22">Edery P</searchLink>; Université Claude Bernard Lyon 1, CNRS, INSERM, Centre de Recherche en Neurosciences de Lyon CRNL U1028 UMR5292, GENDEV, Bron, France.; Service de Génétique, Hospices Civils de, Lyon, France.<br /><searchLink fieldCode="AU" term="%22Delous+M%22">Delous M</searchLink>; Université Claude Bernard Lyon 1, CNRS, INSERM, Centre de Recherche en Neurosciences de Lyon CRNL U1028 UMR5292, GENDEV, Bron, France.<br /><searchLink fieldCode="AU" term="%22Rossi+M%22">Rossi M</searchLink>; Centre de référence des Maladies Osseuses Constitutionnelles, Hospices Civils de, Lyon, France.; Université Claude Bernard Lyon 1, CNRS, INSERM, Centre de Recherche en Neurosciences de Lyon CRNL U1028 UMR5292, GENDEV, Bron, France.; Service de Génétique, Hospices Civils de, Lyon, France.
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