Portal de Periódicos da CAPES

Unique subungueal keratoacanthoma revealing incontinentia pigmenti

2015; Wiley; Volume: 30; Issue: 8 Linguagem: Inglês

10.1111/jdv.13245

1468-3083

M. Ferneiny, S. Hadj‐Rabia, S. Régnier, Nicolás Ortonne, Asma Smahi, Julie Steffann, Jean‐Paul Bonnefont, S. Fraitag, O. Chosidow, Christine Bodemer,

Nonmelanoma Skin Cancer Studies

Journal of the European Academy of Dermatology and VenereologyVolume 30, Issue 8 p. 1401-1403 Letter to the Editor Unique subungueal keratoacanthoma revealing incontinentia pigmenti M. Ferneiny, M. Ferneiny Reference center for genodermatoses and rare skin diseases (MAGEC), Department of Dermatology, Necker-Enfants Malades Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France Institut Imagine, Paris Descartes University - Sorbonne Paris Cité, Paris, FranceSearch for more papers by this authorS. Hadj-Rabia, S. Hadj-Rabia Reference center for genodermatoses and rare skin diseases (MAGEC), Department of Dermatology, Necker-Enfants Malades Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France Institut Imagine, Paris Descartes University - Sorbonne Paris Cité, Paris, France INSERM U1163, Institut Imagine, Paris, FranceSearch for more papers by this authorS. Regnier, S. Regnier Department of Dermatology, Henri Mondor Hospital, Assistance Publique-Hôpitaux de Paris, Créteil, FranceSearch for more papers by this authorN. Ortonne, N. Ortonne Department of Pathology, Hôpital Henri Mondor, Assistance Publique-Hôpitaux de Paris, Créteil, FranceSearch for more papers by this authorA. Smahi, A. Smahi INSERM U1163, Institut Imagine, Paris, FranceSearch for more papers by this authorJ. Steffann, J. Steffann Institut Imagine, Paris Descartes University - Sorbonne Paris Cité, Paris, France Molecular genetics laboratory, Necker-Enfants Malades Hospital, Assistance Publique- Hôpitaux de Paris, Paris, FranceSearch for more papers by this authorJ.-P. Bonnefont, J.-P. Bonnefont Institut Imagine, Paris Descartes University - Sorbonne Paris Cité, Paris, France Molecular genetics laboratory, Necker-Enfants Malades Hospital, Assistance Publique- Hôpitaux de Paris, Paris, FranceSearch for more papers by this authorS. Fraitag, S. Fraitag Reference center for genodermatoses and rare skin diseases (MAGEC), Department of Dermatology, Necker-Enfants Malades Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France Department of Pathology, Necker-Enfants-Malades Hospital, Assistance Publique-Hôpitaux de Paris, Paris, FranceSearch for more papers by this authorO. Chosidow, O. Chosidow Department of Dermatology, Henri Mondor Hospital, Assistance Publique-Hôpitaux de Paris, Créteil, FranceSearch for more papers by this authorC. Bodemer, Corresponding Author C. Bodemer Reference center for genodermatoses and rare skin diseases (MAGEC), Department of Dermatology, Necker-Enfants Malades Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France Institut Imagine, Paris Descartes University - Sorbonne Paris Cité, Paris, France INSERM U1163, Institut Imagine, Paris, France Correspondence: C. Bodemer. E-mail: [email protected] M. Ferneiny and S. Hadj-Rabia contribute equally to this work.Search for more papers by this author M. Ferneiny, M. Ferneiny Reference center for genodermatoses and rare skin diseases (MAGEC), Department of Dermatology, Necker-Enfants Malades Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France Institut Imagine, Paris Descartes University - Sorbonne Paris Cité, Paris, FranceSearch for more papers by this authorS. Hadj-Rabia, S. Hadj-Rabia Reference center for genodermatoses and rare skin diseases (MAGEC), Department of Dermatology, Necker-Enfants Malades Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France Institut Imagine, Paris Descartes University - Sorbonne Paris Cité, Paris, France INSERM U1163, Institut Imagine, Paris, FranceSearch for more papers by this authorS. Regnier, S. Regnier Department of Dermatology, Henri Mondor Hospital, Assistance Publique-Hôpitaux de Paris, Créteil, FranceSearch for more papers by this authorN. Ortonne, N. Ortonne Department of Pathology, Hôpital Henri Mondor, Assistance Publique-Hôpitaux de Paris, Créteil, FranceSearch for more papers by this authorA. Smahi, A. Smahi INSERM U1163, Institut Imagine, Paris, FranceSearch for more papers by this authorJ. Steffann, J. Steffann Institut Imagine, Paris Descartes University - Sorbonne Paris Cité, Paris, France Molecular genetics laboratory, Necker-Enfants Malades Hospital, Assistance Publique- Hôpitaux de Paris, Paris, FranceSearch for more papers by this authorJ.-P. Bonnefont, J.-P. Bonnefont Institut Imagine, Paris Descartes University - Sorbonne Paris Cité, Paris, France Molecular genetics laboratory, Necker-Enfants Malades Hospital, Assistance Publique- Hôpitaux de Paris, Paris, FranceSearch for more papers by this authorS. Fraitag, S. Fraitag Reference center for genodermatoses and rare skin diseases (MAGEC), Department of Dermatology, Necker-Enfants Malades Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France Department of Pathology, Necker-Enfants-Malades Hospital, Assistance Publique-Hôpitaux de Paris, Paris, FranceSearch for more papers by this authorO. Chosidow, O. Chosidow Department of Dermatology, Henri Mondor Hospital, Assistance Publique-Hôpitaux de Paris, Créteil, FranceSearch for more papers by this authorC. Bodemer, Corresponding Author C. Bodemer Reference center for genodermatoses and rare skin diseases (MAGEC), Department of Dermatology, Necker-Enfants Malades Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France Institut Imagine, Paris Descartes University - Sorbonne Paris Cité, Paris, France INSERM U1163, Institut Imagine, Paris, France Correspondence: C. Bodemer. E-mail: [email protected] M. Ferneiny and S. Hadj-Rabia contribute equally to this work.Search for more papers by this author First published: 21 September 2015 https://doi.org/10.1111/jdv.13245Citations: 5Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat No abstract is available for this article. References 1Oliwiecki S, Peachey RD, Bradfield JW, Ellis J, Lovell CR. Subungual keratoacanthoma–a report of four cases and review of the literature. Clin Exp Dermatol 1994; 19: 230–235. 2Baran R, Goettmann S. Distal digital keratoacanthoma: a report of 12 cases and a review of the literature. Br J Dermatol 1998; 139: 512–515. 3Sakai H, Minami M, Satoh E, Matsuo S, Iizuka H. Keratoacanthoma developing on a pigmented patch in incontinentia pigmenti. Dermatology 2000; 200: 258–261. 4Montes CM, Maize JC, Guerry-Force ML. Incontinentia pigmenti with painful subungual tumors: a two-generation study. J Am Acad Dermatol 2004; 50(2 Suppl): S45–S52. 5Baek HJ, Lee SJ, Cho KH et al. Subungual tumors: clinicopathologic correlation with US and MR imaging findings. Radiographics 2010; 30: 1621–1636. 6Allen CA, Stephens M, Steel WM. Subungual keratoacanthoma. Histopathology 1994; 25: 181–183. 7Smahi A, Courtois G, Vabres P et al. Genomic rearrangement in NEMO impairs NF-κB activation and is a cause of incontinentia pigmenti. Nature 2000; 405: 466–472. 8Hadj-Rabia S, Rimella A, Smahi A et al. Clinical and histologic features of incontinentia pigmenti in adults with nuclear factor-κB essential modulator gene mutations. J Am Acad Dermatol 2011; 64: 508–515. 9Donati P, Muscardin L, Amantea A, Paolini F, Venuti A. Detection of HPV-15 in painful subungual tumors of incontinentia pigmenti: successful topical therapy with retinoic acid. Eur J Dermatol 2009; 19: 243–247. 10Martinez-Pomar N, Munoz-Saa I, Heine-Suner D et al. A new mutation in exon 7 of NEMO gene: late skewed X-chromosome inactivation in an incontinentia pigmenti female patient with immunodeficiency. Hum Genet 2005; 118: 458–465. Citing Literature Volume30, Issue8August 2016Pages 1401-1403 ReferencesRelatedInformation